properties of an intergenic terminator and start
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PROPERTIES OF AN INTERGENIC TERMINATOR AND START
SITE SWITCHING THAT REGULATES IMD2 TRANSCRIPTION IN
YEAST
M. Harley Jenks#, Thomas W. O’Rourke
#, and Daniel Reines*
Department of Biochemistry, Emory University School of Medicine
Atlanta, GA 30322
Word count: Materials & Methods-948
Word count: Intro, Results, Discussion-4,718
Running Title: regulated start site selection and termination
#These authors contributed equally to this work.
*Corresponding author
Phone: 404-727-3361
FAX 404-727-2538
Email: dreines@emory.edu
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Copyright © 2008, American Society for Microbiology and/or the Listed Authors/Institutions. All Rights Reserved.Mol. Cell. Biol. doi:10.1128/MCB.00380-08 MCB Accepts, published online ahead of print on 21 April 2008
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SUMMARY
The IMD2 gene in Saccharomyces cerevisiae is regulated by intracellular guanine
nucleotides. Regulation is exerted through the choice of alternative transcription start sites that
results in synthesis of either an unstable short transcript terminating upstream of the start codon
or a full length productive IMD2 mRNA. Start site selection is dictated by the intracellular
guanine nucleotide levels. Here we have mapped the polyadenylation sites of the upstream,
unstable short transcripts that form a heterogeneous family of RNAs of …200 nt. The switch
from the upstream to downstream start sites required the Rpb9 subunit of RNA polymerase II.
The enzyme’s ability to locate the downstream initiation site decreased exponentially as the start
was moved downstream from the TATA box. This suggests that RNA polymerase II’s pincer
grip is important as it slides on DNA in search of a start site. Exosome degradation of the
upstream transcripts was highly dependent upon the distance between the terminator and the
promoter. Similarly, termination was dependent upon the Sen1 helicase when close to the
promoter. These findings extend the emerging concept that distinct modes of termination by
RNA polymerase II exist and that the distance of the terminator from the promoter, as well as its
sequence, is important for the pathway chosen. ACCEPTED
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INTRODUCTION
A large number of short RNAs that do not code for proteins have been identified in
eukaryotic cells. In Saccharomyces cerevisiae many of these are found between conventional
mRNA-encoding transcription units; some of these play a regulatory function in controlling
adjacent gene activity (Martens et al., 2004; Davis and Ares, 2006; Steinmetz et al., 2006b).
IMD2 encodes IMP dehydrogenase, an enzyme important for de novo synthesis of guanine
nucleotides. Its transcription is strongly induced when intracellular guanine nucleotide pools are
depleted by drugs such as mycophenolate and 6-azauracil (Shaw and Reines, 2000; Escobar-
Henriques and Daignan-Fornier, 2001; Hyle et al., 2003). This response enables cells to
maintain adequate guanine nucleotide pools and survive drug exposure. A transcription unit
upstream of IMD2 that generates a short, unstable, non-coding RNA was discovered following
inactivation of an RNA degradation system known as the nuclear exosome (Davis and Ares,
2006). The presence of a transcriptional terminator between the upstream transcription unit and
the downstream unit encoding IMD2 mRNA was inferred in a genome-wide analysis of RNA
polymerase II density on yeast chromosomes (Steinmetz et al., 2006b). Comparison of wildtype
and sen1 mutant strains revealed a downstream shift in RNA polymerase II density toward the
IMD2 ORF, suggestive of terminator readthrough (Steinmetz et al., 2006b) since SEN1 encodes
an essential helicase known to be involved in transcription termination (Steinmetz and Brow,
1996; Rasmussen and Culbertson, 1998; Steinmetz et al., 2001; Steinmetz et al., 2006a; Kim et
al., 2006). Furthermore, there is a regulated shift from a set of upstream transcription start sites
(Fig. 1, thin arrows) to a single downstream adenine start site (Fig. 1, thick arrow) when levels of
intracellular guanine nucleotides become depleted (Davis and Ares, 2006; Steinmetz et al.,
2006b; Kuehner and Brow, manuscript submitted). Under guanine-replete conditions, the
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upstream start predominates and transcription terminates before the IMD2 ORF is reached,
resulting in production of a short, non-coding RNA. This ‘intergenic’ transcript is rapidly
degraded in an exosome-dependent manner (Davis and Ares, 2006). Under guanine-depleted
conditions, the start site downstream of the termination region is used resulting in full length
IMD2 mRNA encoding IMP dehydrogenase. Deletion or mutation of the terminator region
(previously referred to at the Repressive Element; underlined in Fig. 1) was shown to de-repress
IMD2 expression enabling its transcription even when guanine is plentiful (Shaw et al., 2001;
Escobar-Henriques-Henriques and Daignan-Fornier, 2001). As well, the terminator region
possesses autonomous terminator function when placed downstream of a promoter where it can
generate polyadenylated transcripts (Kopcewicz et al., 2007). This terminator is unusual in that
it overlaps the transcription start site employed when IMD2 transcription is induced by low
guanine nucleotide levels (Fig. 1). This explains why it is required to maintain the repressed
state of the IMD2 ORF since when this DNA is deleted or mutated, transcription reads into the
IMD2 ORF from the upstream start events that are normally aborted by termination when
guanine levels are adequate. Here we will refer to this novel terminator as the intergenic-IMD2
terminator (IT) because it is responsible for the formation of a discrete intergenic transcript.
Termination by RNA polymerase II is poorly understood. For conventional terminators
at the end of mRNA transcription units, RNA polymerase II ceases elongation and disengages
from chromatin in a manner coupled to the processing of the 3’-end of the RNA; i.e. cleavage of
the primary transcript and its polyadenylation (reviewed in Buratowski, 2005; Rosonina et al.,
2006). Recent evidence suggests there is more than one mechanism of transcription termination
by RNA polymerase II, depending upon the gene being transcribed. Small nuclear (sn) and
nucleolar (sno) RNAs which are relatively short and are not polyadenylated in their mature form,
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employ an alternative system that involves the Sen1 helicase and the Nrd1 and Nab3 RNA
binding proteins (Steinmetz et al., 2001; Kim et al., 2006; Steinmetz et al., 2006a). An
additional set of components appears to be shared by the two termination/processing systems
including Pcf11, Rna14, Rna15, and Ssu72 (Steinmetz and Brow, 2003; Rosonina et al., 2006;
Arigo et al., 2006; Kim et al., 2006; Lykke-Anderson and Jensen, 2007). One determinant of the
termination mechanism to be employed is the distance between the termination region from the
transcription start site (Steinmetz et al., 2006a; Kopciewicz et al., 2007).
Recent evidence indicates that termination of one group of short non-coding RNAs is
coupled to their rapid degradation by the exosome (Arigo et al., 2006; Thiebaut et al., 2006;
Vasiljeva and Buratowski, 2006). The terminator at the end of the transcription unit upstream of
IMD2 appears to fall into this class (Davis and Ares, 2006; Steinmetz et al., 2006b; Kopciewicz
et al., 2007). Previous results suggested that Nrd1-dependent termination is most active at a
short distance from the transcription start site; whereas conventional cleavage and
polyadenylation operate at more distal downstream sites such as those at the end of protein-
encoding mRNAs (Steinmetz et al., 2006a).
Here we explore the requirements for termination at the intergenic-IMD2 terminator and
compare it with the canonical terminator/polyadenylation site found at the end of the CYC1 gene.
The RNA generated by the intergenic-IMD2 terminator is rapidly degraded by the nuclear
exosome, a phenomenon seen only when the sequence is placed close to a promoter. In contrast,
the CYC1 terminator yields a stable RNA even when close to the promoter. As well, the
intergenic-IMD2 terminator is highly Sen1-dependent compared to the CYC1 terminator.
Grafting a portion of the intergenic-IMD2 terminator containing a Nab3 consensus site onto the
CYC1 terminator enhanced its exosome-sensitivity. Increasing the distance between the
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upstream start sites and the terminator resulted in longer intergenic terminated transcripts and
prevented use of the downstream start site, consistent with a model in which RNA polymerase II
scans along DNA for a start site. Furthermore, the guanine regulated shift from the upstream to
downstream start sites was highly dependent upon the Rpb9 subunit of RNA polymerase II,
accounting for the extreme drug-sensitivity of cells lacking this RNA polymerase II subunit and
emphasizing the importance of RNA polymerase II’s “jaw” in grasping DNA during
translocation.
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MATERIALS AND METHODS
Plasmid Construction: The plasmids pGAlLuc, pREFXba-Luc, pRERXba-Luc, pREFBstEII-Luc
and pRERBstEII-Luc have been previously described by our lab (Shaw et al., 2001; Kopcewicz
2007). The lambda insertion family of plasmids were derived from pRS316-IMD2-BsiWImut
which was made by mutagenesis using mismatch oligonucleotides 5’-
gcttacattttacctcgtacgctgggaacc-3’ and 5’-ggttcccagcgtacgaggtaaaatgtataagc-3’ to introduce a
BsiWI restriction site … 180 bp upstream of the start codon in plasmid pRS316-IMD2 (Hyle et
al., 2003). pRS316-IMD2-24bpn, pRS316-IMD2-36bpn, pRS316-IMD2-45bpn, pRS316-
IMD2-103bpn, pRS316-IMD2-153bpn, and pRS316-IMD2-218bpn were made by inserting
HaeIII or BstUI digested lambda DNA of less than 250 bp into pRS316-IMD2-BsiWImut cut
with BstWI and filled in with DNA polymerase. A distribution of clones with increasing insert
sizes were selected for confirmation by sequencing.
A DNA duplex encoding the 5’ end of the IT and the CYC1 transcription terminator was
cut with XbaI and inserted into similarly cut pGalLuc to create pChimera1-F-XbaLuc. This
chimeric piece of DNA was made by annealing 5’-
agctcatctagattccgtattctattctattccttgccttacttttcttattattttctatttatttttt-3’ and
gatcgatctagagtataatgttacatgcgtacacgcgtctgtacagaaaaaaaagaaaaatttgaaatataaataacgttcttaatactaacata
actataaaaaaataaata-3’ and extending each primer via mutually primed synthesis with T4 DNA
polymerase. The same product in the opposite orientation was also inserted into pGalLuc to
form pChimera1-R-XbaLuc. The plasmid pCYC1TT-F-XbaLuc was made by inserting an XbaI
digested PCR product encoding the CYC1 transcription terminator region into XbaI cut pGalLuc.
The PCR product was generated from pYES2 (Invitrogen) using the primers 5’-
agctcatctagagacaacctgaagtctagg-3 ’ and 5’-gatcgatctagagtataatgttacatgcgt-3’. A similar BsiWI-
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digested PCR product was generated from pCYC1TT-F-XbaLuc using the oligonucleotides 5’-
agctcacgtacggacaacctgaagtctagg-3’ and 5’-gatcgacgtacggtataatgttacatgcgt-3’ for insertion of the
CYC1 terminator into the BsiWI site of pGalLuc to form pCYC1TT-F-BsiLuc. The plasmid
pChimera-F-BsiLuc was assembled by inserting a BsiWI-digested PCR product made off
pChimera1-F-XbaLuc with primers 5’-agctcacgtacgttccgtattctattctat-3’ and 5’-
gatcgacgtacggtataatgttacatgcgt-3’.
The plasmid pGalNabMutXba-F-Luc was made by inserting into XbaI-digested pGalLuc
an XbaI-digested PCR product with the IT containing a site directed mutation of the putative
Nab3 site. This PCR product was generated from plasmid pREFXbaLuc using 5’-
agctcatctagattccgtattctattctattccttgccttactttagttattattttc-3’ which contains the mutation and 5’-
gatcgatctagaaacaaaatgcgtttatgacag-3’.
Strains: Strains DY682-DY689 were made by transforming wildtype and sen1E1597K
strains (46a
and sen1E1597K
; D. Brow, U. Wisconsin, Madison) with the plasmids pREFXbaLuc,
pRERXbaLuc, pREFBstLuc, and pRERBstLuc as indicated in Table I. DY695 was constructed
by transforming Open Biosystems’ FRRP6 yeast strain (YSC1021-551682) with the IMD2 gene
disruption cassette from pUC19-IMD2KO (Hyle et al., 2003). Integration of the IMD2 knockout
was confirmed by sequencing of PCR products. Strains DY1701-1708 were made by
transformation of DY695 with the indicated plasmids (Table I) using the lithium acetate method
(Gietz et al., 1992). DY1562 and DY1563 were made by transforming the plasmid
pGalNabMutXba-F-Luc into BY4741 and YSC1021-551682, respectively.
PolyA analysis: To identify the polyA addition sites we used a derivative of the rapid
amplification of cDNA ends-polyA test (RACE-PAT) assay (Salles et al., 1999). Total RNA
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from the rrp6F-strain YSC1021-551682 (Open Biosystems, Inc.) was reverse transcribed with
Moloney murine leukemia virus reverse transcriptase and the oligo-dT-anchor oligonucleotide,
5’-gggaattcgacctcgtcttgcaccttgaagttttcctgttttttttttttttt-3. After heat inactivation of the enzyme, this
cDNA was amplified by PCR using an anchor oligonucleotide 5’-gggaattcgacctcgtcttgcacc-3’,
and an IT-specific oligonucleotide 5’-cgggatccttccgtattctattctattccttgc-3’, digested with EcoRI
and BamHI, ligated into similarly cut pBluescript-KS (Stratagene, Inc.), and transformed into E.
coli. Plasmid was prepared from insert-containing transformants and sequenced.
RNA and Northern blots: Cells were grown in liquid media, collected in the logarithmic growth
phase, washed once with water, and frozen. Total RNA was isolated from thawed cell pellets by
hot acid phenol extraction and quantified by measuring absorbance at 260 nm. Total RNA (15-
30 µg) was resolved on a 1% (w/v) agarose-formaldehyde gel and blotted onto Zeta-probe GT
nylon (Bio-Rad) or Hybond XL (Amersham). Filters were baked at 85°C for 2 h and then pre-
hybridized for a minimum of 3h at 42°C in 5x SSC (1x SSC = 0.15 M NaCl, 0.015 M sodium
citrate), 5X Denhardt's solution, 50% (v/v) formamide, 1% (w/v) SDS, and 100 µg/ml salmon
sperm DNA. Filters were hybridized under the same conditions with 50 oCi of 32
P-labeled DNA
probe for 4h at 30°. Filters were washed at least twice at 42°C in 2x SSC/0.1% SDS for 15 min
each. Washed filters were exposed to Kodak X-Omat or Pierce CL–Xposure film or for
quantification, a phosphorimager screen read by a Fujix BAS1000. Probes were labeled with
Klenow DNA polymerase (NEB), random hexamer primers, and [c/32P]-dATP (Amersham
Biosciences or Perkin-Elmer). For probing transcripts from the GAL1 promoter-terminator
plasmids, a promoter proximal PCR probe was generated from pGalLuc (Shaw et al., 2001)
using the primers 5'-atactttaacgtcaaggagaaaaaacc-3' and 5'-tgttcacctcgatatgtgcatctgtaa-3'. The
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SED1 probe was prepared by PCR from yeast genomic DNA using 5’-
ccgaattccactgattgctccacgtcat-3’ and 5’-ccggatccttacacgcaacgcgtaagaa-3’. To probe northern
blots for the transcripts from IMD2-containing plasmids and chromosomes (Figs. 5 and 6), the
‘upstream’ probe from the IMD2 locus was generated by PCR using 5’-
gactagtgcggccgcatcggttgagcgcgatatta-3’ and 5’-ctgatcaggatccggccattgcttttgctactt-3’ and yeast
genomic DNA. The ‘downstream’ probe was a PCR product made from yeast genomic DNA
using 5’-gtggtatgttggccggtactaccg-3’ and 5’-tcagttatgtaaacgcttttcgta-3’ as described previously
(Kopcewicz et al., 2007).
Primer extension: 5’-32
P labeled, HPLC-purified oligonucleotide (1.5 pmol;
gcgtttatgacagttaaaaag) was mixed with 20 µg of total RNA from the indicated yeast strains,
dried, dissolved in 10 ol of 2 mM Tris, pH 8.1, 0.2 mM EDTA, and 250 mM KCl and annealed
at 65°C for 5 min followed by a 1 hr incubation at 45 °C. Twenty five ol of 55 mM Tris-HCl,
pH 8.1, 9 mM MgCl, 1 mM dithiothreitol, and 500 µM of each dNTP were added to annealing
reactions. The primers were extended with 200 units of M-MLV reverse transcriptase
(Invitrogen) at 37°C. Samples were ethanol precipitated, dissolved in 5 µl of 90 mM Tris borate,
pH 8, 2 mM EDTA, 80% (v/v) formamide, heated to 95°C, and resolved on an 8%
polyacrylamide-7M urea gel.
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RESULTS
Mapping the 3’-ends of the upstream non-coding RNA
To understand the complexity of the IMD2 promoter we set out to define the beginning
and end of the short intergenic transcripts resulting from transcription termination at the
intergenic-IMD2 terminator. While initiation sites have been mapped, the sites at which polyA+
tails are added are unknown. Using reverse transcription from a poly dT primer and a primer
specific for sequences upstream of IMD2, we obtained cDNAs from an RRP6 deletion strain of
S. cerevisiae. Deletion of RRP6 stabilizes short, intergenic non-coding RNAs that would
otherwise be degraded by the exosome (Davis and Ares, 2006). Sequencing of eleven clones
identified sites at which the RNA was polyadenylated (Fig. 1, circled bases). PolyA tails varied
from 11 to 50 bases and the set of addition sites extended over a 78 base interval. All polyA tails
were added at positions downstream of the “low guanine” start site (thick arrow), and almost all
addition sites were at UA or CA dinucleotides as is common in yeast (Graber et al., 2002). The
terminator region contains the four sequence elements present in many yeast termination/polyA
signals and scored highly in a polyA site prediction algorithm (data not shown; Graber et al.,
2002). These 3’-map positions, combined with the spectrum of upstream guanine initiation sites
(Steinmetz et al., 2006b), means that under guanine-replete conditions, short transcripts of 75 to
211 bases (exclusive of polyA) can be synthesized depending upon which pair of initiation and
polyadenylation sites are used (Fig. 1). This range is consistent with the short transcripts
observed earlier on northern blots (Davis and Ares, 2006; Steinmetz et al., 2006b).
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Comparison of the IMD2 intergenic terminator and the CYC1 transcription terminator.
We previously developed a reporter assay for the termination activity of the intergenic-
IMD2 terminator (previously referred to as Repressive Element [RE], referred to here as IT; Fig.
1, underlined) based on its ability to generate short polyA+ transcripts when it was placed
downstream of the GAL1 promoter (Kopciewicz et al., 2007). We used this assay to compare the
IT to a well-characterized conventional terminator derived from the end of the CYC1 gene (Zaret
and Sherman, 1982; Osborne and Guarente, 1989). As described before, when located 120 bp
downstream of the GAL1 start site, the IT efficiently stopped transcription and prevented full
length transcript accumulation following galactose induction (Kopcewicz et al., 2007; Fig. 2;
lanes 1-3). The terminated transcript only became detectable when RRP6 was deleted (Fig. 2;
lanes 4-6). In contrast, when transcription was driven into the CYC1 termination element, a
prominent terminated RNA was detected regardless of RRP6 status (Fig. 2, lanes 7-9 vs 10-12).
Control full length transcripts were also unaffected by deletion of RRP6 (lanes 13-15 vs 16-18).
A similar result was obtained when both elements were inserted 15 bp closer to the promoter
(data not shown). When the IT is moved 110 bp further downstream, however, the terminated
transcript is stable even in the presence of RRP6 (Kopciewicz et al., 2007). Thus, the distance
from the promoter is important for stability of the terminated transcript generated from the IT but
not the CYC1 terminator. This suggests that both distance from the promoter and specific
sequences at the terminator are determinants of transcript handling by the nuclear exosome.
To test the sequence requirement, we grafted 49 bp of the IT (approximately the 5’-half;
Fig. 1, double underline) onto the minimal CYC1 terminator and placed that under GAL1 control.
This piece of the IT is known to be insufficient for termination (Kopcewicz et al., 2007). The
chimeric element efficiently terminated transcription (Fig. 3A; lanes 1-6). The RRP6-
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dependence of the RNAs generated by termination due to the IT, CYC1, and chimeric
terminators, was quantified by phosphorimaging at the 90 min induction time point and
normalizing to a constitutive reference transcript (SED1). Transcripts terminated by the IT in
wildtype strains were 9% as abundant as when the Rrp6 exosome subunit was deleted (lanes 13-
15 vs 16-18 ). This is in striking contrast to the CYC1 terminator in which almost all of the RNA
was stable when the exosome was intact (87% RRP6+ vs Frrp6; lanes 7-9 vs 10-12). The
upstream portion of the IT endowed the CYC1 terminated transcript with increased sensitivity to
the exosome (RRP6+ 39% of rrp6F; lanes 1-3 vs 4-6) when grafted onto its 5’-end, rendering the
transcript more like that generated by the IT than the CYC1 terminator. When the chimeric
construct was moved downstream an additional 110 bp, to a position in which even the IT is
immune to exosome degradation (Kopcewicz et al., 2007), the chimera was also relatively Rrp6-
independent (Fig. 3B; lanes 1-3 vs 4-6) as was the CYC1 terminator (lanes 7-9 vs 10-12).
The Nab3 RNA binding protein has been implicated in termination and degradation of
small RNAs in yeast (Steinmetz et al., 2001; Arigo et al., 2006; Vasiljeva and Buratowski, 2006;
Thiebaut et al., 2006; Kim et al., 2006). The IT has a consensus Nab3 binding site (UCUU).
This site was contained in the portion of the IT grafted to the CYC1 (Fig. 1) and could be part of
the signals for termination and turnover of the non-coding small transcript. We mutated this site
to AGUU in the reporter plasmid in which it is placed downstream of the GAL1 promoter. The
plasmid was introduced into RRP6+ and Frrp6 strains and transcription was induced with
galactose. Mutation of this putative Nab3 site strongly stabilized (5.8 fold) the terminated short
RNA in cells containing an intact exosome (RRP6; Fig. 3C). Interestingly, the mutation did not
improve readthrough, i.e. it did not reduce termination efficiency of the IT. This contrasts with a
point mutation 10 bp downstream of UCUU that essentially abrogates termination giving rise to
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a stable full length RNA (Kopcewicz et al., 2007). Thus, separate sequences in the IT provide
for the termination and RNA degradation functions. There is a slight increase in abundance of
the terminated transcript in a Frrp6 strain (1.4 fold), suggesting that the transcript may be
degraded by residual activity of the Rrp6-depleted nuclear exosome or another nuclease pathway
(Frrp6; Fig. 3C). These results are consistent with experiments in a nab3 mutant strain that also
suggests a role for this protein in IT function (Kuehner and Brow, manuscript submitted).
Position-dependence of Sen1-mediated termination.
Sen1 is strongly implicated in termination at the IT (Steinmetz et al., 2006b). We tested
its role directly by transcribing the reporter construct in a strain bearing the temperature sensitive
sen1E1597K
allele. In a strain wildtype for SEN1, the IT promoted termination and yielded trace
levels of an unstable transcript (Fig. 4A; lanes 1-4, solid arrow). In contrast, the sen1 mutation
rendered the terminator significantly less effective at both the permissive and restrictive
temperatures (lanes 5-8). Presumably these longer transcripts escape exosome attack thereby
explaining their higher level of accumulation compared to terminated RNAs in lanes 1-6. If the
Sen1 termination mechanism operates preferentially on short transcripts in concert with the
exosome, then moving the IT downstream should abrogate the ability of the sen1E1597K
mutation
to cause readthrough of the terminator. Indeed the IT shows strong termination when positioned
680 bp downstream from the start site regardless of the status of SEN1 (lanes 9-12 vs 13-16).
The sen1E1597K
mutation had no effect on readthrough even at the restrictive temperature when
the IT was in this location (lanes 13-16). Overall RNA abundance was also higher when the IT
was this far downstream since the transcripts were not diverted to the exosome degradation
pathway (lanes 10, 12, 14, 16). This demonstrates a strong position-dependence to Sen1’s
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termination function. The CYC1 terminator is also dependent upon the Sen1 pathway (Steinmetz
et al., 2006b). It is a canonical polyA-signal/termination site found at the end of the ORF. The
CYC1 terminator was 77% effective as a terminator in a SEN1+ strain at either permissive or
restrictive temperatures when located close (120 bp) to the transcription start site (Fig. 4B, lanes
1-6). The sen1E1597K
mutation reduced termination efficiency (short transcripts divided by total
transcripts) to 43% and 28% at the permissive and restrictive temperatures, respectively (Fig. 4B,
lanes 7-9 and 10-12) in a manner similar to the mutation’s effect on the IT and as seen before in
another reporter system (Steinmetz et al., 2006b). These results confirm that Sen1 influences
terminator function for both terminators but only IMD2’s IT renders terminated RNA sensitive to
exosome degradation. Therefore, termination and degradation of short transcripts are not
obligatorily coupled.
Effect of distance upon RNA polymerase II’s ability to switch initiation sites.
We next asked if the distance between the two types of initiation sites (Fig. 1, the
upstream Gs vs the downstream A) was important for their regulated selection, for example if
RNA polymerase slides between them when making its initiation decision. To test this, we
introduced a BsiWI restriction site (Fig. 1; targeted sequence is boxed) between the initiation
sites for high guanine and the low guanine start into which we inserted random pieces of DNA
from lambda phage of varying size (24, 36, 45, 103, 153, and 218 bp). Plasmids with these
‘lengthened’ versions of IMD2 were introduced into a yeast strain deleted for chromosomal
IMD2 and the transcription start site patterns of the lengthened constructs were analyzed. Start
site mapping by primer extension revealed that the normal high guanine start sites were still used
when cells were grown in guanine (Fig. 5A; odd numbered lanes). (Although more complex
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initiation patterns are apparent for the two largest inserts.) In contrast, when the cells were
grown in mycophenolic acid, RNA polymerase II’s ability to start from the normal downstream
A-residue was gradually compromised with increasing distance (Fig. 5A; ‘low G (MPA) start’ in
even numbered lanes, and graph). These results suggest that either RNA polymerase II abandons
its search for a start site or finds alternative start sites before the IT. In the latter case, transcripts
started upstream of the IT would terminate, be degraded, and fail to produce any protein-
encoding IMD2 mRNA. To examine this, we performed northern analysis on the transcripts
produced from these constructs in RRP6-deletion strains, using a probe that detects the upstream
short transcript and full length downstream transcripts (Fig. 5B, upper panel) or just the
downstream transcripts containing approximately the 3’-half of the IMD2 ORF (lower panel).
As expected, long transcripts were produced at the expense of short RNAs from wildtype IMD2,
as well as from the IMD2 in which we engineered a new restriction site (upper panel, lanes 1 vs 3
and 4 vs 6). The addition of 24 bp of lambda DNA between the upstream and downstream
initiation sites did not influence this pattern (lanes 7-9). When larger pieces of DNA were
inserted, MPA-induction of full length RNAs detected by either probe was reduced (36 bp, lane
12) or virtually absent (45, 103, 153, 218 bp; lanes 15, 18, 21 and 24, respectively). Thus, RNA
synthesis from any start site was curtailed when RNA polymerase II was unable to find the
favored downstream A-start site in the presence of MPA. The lack of short or long RNA
production in the presence of MPA (lanes 15, 18, 21, and 24) also strongly suggests that no other
start sites are found as alternatives, either up or downstream of the natural initiation site unless
such aberrant RNAs are degraded by a nuclease system other than that requiring RRP6.
Since IMD2 expression is required for growth in the presence of MPA, the absence of full
length IMD2-encoding mRNA in these strains should render them MPA-sensitive. This was
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indeed the case, as growth was proportional to expression of full length IMD2 mRNA where the
36 bp insert allowed some growth but larger inserts did not support any (Fig. 5C). Hence, the
regulated switch from transcription of the upstream short RNA to the downstream biologically
active IMD2 mRNA can be disrupted by perturbing the choice of transcription initiation site.
The role of the Rpb9 subunit of RNA polymerase II in IMD2 start site selection.
To further examine the start site shift, we studied initiation in a strain of yeast deleted for
RPB9. This small subunit of RNA polymerase II is not essential but its loss shifts transcription
start sites upstream and impairs elongation more generally (Furter-Graves et al., 1994; Hull et
al., 1995; Sun et al., 1996; Awrey et al., 1997; Hemming et al., 2000). It also renders cells
extremely MPA-sensitive as well as defective in IMD2 induction (Shaw et al., 2001). This
suggested that RNA polymerase lacking this subunit might have a start site switch problem on
IMD2 during induction. Primer extension (Fig. 6A) and northern blotting (Fig. 6B) showed no
detectable IMD2 transcripts in an RPB9-null strain following MPA treatment (Fig. 6A, lanes 7-9;
Fig. 6B, lanes 4-6). As seen before, when RRP6 was deleted in order to stabilize the small
intergenic transcripts, the upstream guanine initiation sites were detectable by primer extension
in a strain with intact RPB9 (Fig. 6A, lane 4). When challenged with MPA, the downstream
‘low-guanine’ start was observed (Fig. 6A, lane 6). When RRP6 was deleted in order to stabilize
the intergenic transcripts in the RPB9-deletant, we found that RNA polymerase II could employ
the ‘high-guanine’ starts (Fig. 6A, lanes 1 and 2) but they were shifted upstream relative to
RPB9. More importantly, the RPB9-deletants were not capable of utilizing the downstream
initiation site normally induced by MPA (Fig. 6A, lane 3 vs lane 6). This is a likely explanation
for why an RPB9 deletion strain is so sensitive to MPA. Northern blotting of the Frpb9 Frrp6
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double deletant (Fig. 6B) confirmed this start site shift defect since short intergenic transcripts
were synthesized normally, but full length mRNA could not be induced (lane 1 vs lane 7 and
lane 3 vs lane 9).
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DISCUSSION
Regulation of IMD2 employs an unusual mechanism involving a non-coding transcript
arising from upstream of the productive transcription start site. This non-coding RNA is
degraded since its synthesis is not as important as the fact that polymerase molecules
preferentially initiate at an upstream site when GTP is available and terminate at the IT, thereby
preventing use of a downstream start that would otherwise produce IMD2 coding mRNA. Brow
and co-workers have shown that start site selection is governed by RNA polymerase’s choice of
GTP vs ATP as the initiating nucleotide, with the upstream G-starts preferred when guanine
nucleotide pools are adequate and the alternate downstream start site employed when GTP is
limiting (Steinmetz et al., 2006b, Kuehner and Brow, manuscript submitted; Fig. 1). This
preference probably explains why the region has evolved an unusual sequence bias of only 13%
G between the TATA box and initiation codon whereas the IMD2 ORF is 23% G and all ORFs
average 21% G. The 97 bp terminator element itself, in which the low-G adenine start site lies,
is a strikingly low 6% G. Under this scenario, the productive downstream start site is not
accessed unless GTP levels are low enough that the upstream starts can not be employed because
RNA polymerase II is essentially starved for that nucleotide at those positions. Thus, the option
of two start sites appears to be largely a mutually exclusive choice.
Here we delineate the intergenic transcripts’ boundaries by identifying their 3’-ends. The
short transcripts are a family of polyA+ RNAs potentially ranging from 75 nucleotides to slightly
over 200 nucleotides. The polyA-addition sites all fall downstream of the adenine start site that
generates IMD2 mRNA and which is centrally located in the terminator (Fig. 1). Hence, at the
MPA-induced start site, RNA polymerase initiates inside the terminator and can not transcribe
the full set of sequences required for termination at the IT. By mapping RNA polymerase II
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density using a chromatin immunoprecipitation-microarray (ChIP-chip) assay, readthrough of the
IT in a sen1 mutant strain was observed (Steinmetz et al., 2006). Here we show directly that the
IT’s activity is Sen1-dependent. As predicted from work on short transcript termination
(Steinmetz et al., 2001; Kim et al., 2006; Thiebaut et al., 2006; Arigo et al., 2006; Steinmetz et
al., 2006b), we also observed that the role of Sen1 in termination is strongly distance dependent;
it failed to affect termination when the IT was 680 bp from the start site (Fig. 4A). Termination
was nevertheless efficient and therefore has been subsumed by an alternative termination
mechanism. The IT terminator functioned autonomously to yield a transcript that was very
sensitive to degradation by the exosome, but again only when it was positioned close to an
initiation site. This was unique to the IMD2 IT since transcripts generated by the canonical
CYC1 terminator were not susceptible to degradation at that distance but could be made so by
transferring a piece of the IT upstream of the CYC1 terminator. Therefore, a sequence
determinant as well as distance influences the fate of the terminated transcript. A good candidate
for the relevant sequence is a Nab3 consensus site found in the region (Fig. 3C and Kuehner and
Brow, manuscript submitted). These findings also fit with a model in which different classes of
RNA polymerase II transcripts are terminated by different systems. One system employs the
RNA binding proteins Nab3 and Nrd1 along with the Sen1 helicase (Steinmetz et al., 2001;
Steinmetz and Brow, 2003; Carroll et al., 2004; Steinmetz et al., 2006b; Vasiljeva and
Buratowski, 2006; Kim et al., 2006). Short transcripts, such as non-coding regulatory RNAs and
snRNA/snoRNAs use this system. Handling of the former set of transcripts is also coupled to
rapid degradation by the exosome, as observed here (Davis and Ares, 2006; Arigo et al., 2006;
Thiebaut et al., 2006).
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What could account for the strong distance dependence of Sen1 activity and exosome
stimulating activity we observed for this terminator? An obvious candidate is the
phosphorylation state of the carboxyl terminal domain (CTD) of the large subunit of RNA
polymerase II. Since the phosphorylation pattern changes as a function of where in the
transcription cycle polymerase is, it is attractive to consider that the transcribing enzyme matures
over the transcription unit with respect to phosphorylation and loading of the Sen1 termination
machinery onto the elongation complex. Serine 5 phosphorylation of the CTD repeat is enriched
in the 5’-end of transcription units whereas serine 2 phosphorylation is enriched at the 3’-end
(Phatnani and Greenleaf, 2006). It has been postulated that these markings are signals for the
different co-transcriptional events that process primary transcripts into mature mRNA
(Komarnitsky et al., 2000). Once a transition point has been reached, Sen1 can no longer gain
access to the complex and the window of opportunity for that termination system to operate has
passed. A role for Nrd1 and Nab3 in engaging the complex early after initiation is attractive as
these proteins are known to associate with each other and Nrd1 binds the CTD (Conrad et al.,
2000; Carroll et al., 2007). As well, the CTD kinase CTK1 has been linked to the
Sen1/Nrd1/Nab3 termination system (Conrad et al., 2000). Recent work has shown that Nrd1
recognizes Ser-5 phosphorylated RNA polymerase II and phosphorylation at serine-7 has
recently been identified that is specific for snRNA synthesis (Egloff et al., 2007; Vasiljeva et al.,
2008). Hence, there is enough variety in the modification of an elongation complex to provide
signals to distinct termination machineries over the course of transcription.
Our results in modifying the spacing between the upstream and downstream start sites
reveal an exponential decay in the ability of RNA polymerase II to recognize an initiation site
that is progressively more distant from the TATA box (Fig. 5A). These data are consistent with
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a scanning model for RNA polymerase II in which the enzyme enters chromatin through
recognition of the pre-initiation complex, melts DNA, and tracks on the template until it finds a
satisfactory initiation site (Giardina and Lis, 1993; Leuther et al., 1996; Kuehner and Brow,
2006). Given the regulatory role of guanine nucleotide concentration in this case, and the unique
nature of the high guanine start sites (rare tandem GG dinucleotides, Kuehner and Brow,
manuscript submitted), sliding between start sites would likely take place without chain
initiation. However, the possibility that small oligonucleotides such as abortive transcripts are
made and released during this search, cannot be excluded. The distance effect may also
represent the difficulty RNA polymerase has in making contact with proteins that reside
upstream such as TFIID. With respect to the start site decision at IMD2, it will be interesting to
examine the role of TFIIB in this process since it is part of the measuring device that positions
start sites at a fixed point downstream of the TATA box (Pinto et al., 1992; Pinto et al., 1994; Li
et al., 1994; Leuther et al., 1996; Chen and Hampsey, 2004; Bushnell et al., 2004). In the case
of IMD2, start site selection is a regulated variable so for this unusual promoter there is plasticity
in this feature.
Our experiments with strains lacking the Rpb9 subunit help elucidate why those cells are
so sensitive to MPA and why they fail to induce IMD2. RNA polymerase II without this subunit
initiates at the upstream site but cannot initiate from the A-start downstream. This makes sense
since Rpb9 is known to play a role in start site positioning generally and is a significant
component of one of the pincers of the enzyme’s jaws that contacts downstream duplex DNA
(Furter-Graves et al., 1994; Hull et al., 1995; Hemming et al., 2000; Cramer et al., 2001).
Absence of the subunit may result in a structural deficit, such as a loose grip on DNA, that
hampers controlled translocation of the enzyme. This could also explain the importance of Rpb9
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in: 1) general elongation, 2) the RNA cleavage activity of the enzyme, which involves reverse
translocation, and 3) proofreading, which in turn relies on RNA cleavage and translocation
(Awrey et al., 1997; Hemming et al., 2000; Nesser et al., 2006; Koyama et al., 2007). If RNA
polymerase II deficient in Rpb9 slides on DNA between these two possible start sites, it will be
interesting to know if it is released from the upstream transcription unit following its failure to
find the downstream start site, or remains bound to DNA.
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ACKNOWLEDGEMENTS
We thank Dr. D. Brow for materials and information prior to publication, Dr. J. Boss for
a critical reading of the manuscript, and Katrina Kopcewicz for contributing to early portions of
this study. This work was supported by NIH grant GM46331.
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FIGURE LEGENDS
Figure 1- Sequence of the IMD2 promoter region. Initiation sites in the presence of guanine are
indicated with thin bent arrows. The initiation site when guanine is limiting is depicted with the
thick bent arrow (Steinmetz et al., 2006b). Map positions at which polyA is added to IT-
terminated, intergenic RNAs are circled. The TATA box (per Escobar-Henriques et al., 2003)
and start codon are shown in large type. The IT is identified with a solid underline (single and
double). The portion of the IT used to create a chimeric terminator is doubly underlined. The
hexamer mutagenized to a BsiWI site (AGTATG å CGTACG) is boxed. The consensus Nab3
binding site is in a shaded box.
Figure 2- Exosome sensitivity of the IT and CYC terminated transcripts. RNA was prepared for
northern analysis from yeast strains wildtype or deleted for RRP6 and bearing a plasmid
containing the GAL1 promoter and either the CYC1 or IMD2 intergenic terminator (IT) inserted
downstream of the promter (indicated schematically at the bottom of the figure). [Strains were,
from left to right, DY1038, DY1403, DY1532, DY 1534, DY1035, and DY1400.] Cells were
induced with 2% galactose for 0, 30, or 90 min and probed with the GAL1 or the SED1 (as a
loading control) probes, as indicated.
Figure 3- Exosome sensitivity of terminated transcripts. RNA was prepared for northern analysis
from yeast strains wildtype or deleted for RRP6 and bearing a plasmid containing the GAL1
promoter and either the CYC1 terminator, the IT, or a chimera between the CYC1 and IMD2-IT.
The chimera contained 49 bp of the IT (double underlined in Fig. 1) placed 5’ to 102 bp of the
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CYC1 core terminator (there was a 4 bp overlap of common sequence between them).
Terminators were inserted at proximal (XbaI, panel A) or distal (BsiWI, panel B) positions
downstream of the promoter (indicated schematically at the bottom of the figure). [Strains were
DY1550 (part A, lanes 1-3), DY1551 (lanes 4-6), DY1532 (lanes 7-9), D1534 (lanes 10-12),
DY1038 (lanes 13-15), DY1403 (lanes 16-18) DY1554 (part B, lanes 1-3), DY1555 (lanes 4-6),
DY1558 (lanes 7-9) and DY1559 (lanes 10-12)]. Transcription was induced following galactose
exposure for the indicated times. Filters were probed with the GAL1 or SED1 probes as
indicated. Full length (IT in the reverse orientation in the XbaI site) marker RNA from
galactose-induced DY1552 was loaded in the lane marked M. In panel C, transcription through
an IT with a mutated consensus Nab3 binding site (AGUU) or an unaltered site (UCUU) was
analyzed by northern blotting as described in parts A and B.
Figure 4- SEN1-dependence of termination. RNA was prepared for northern analysis from
wildtype yeast and strains with the Sen1E1597K
mutation. Each strain contained plasmids with the
GAL1 promoter and either the CYC1 terminator or the IMD2 IT inserted downstream of the
promoter. Terminators were inserted at promoter proximal (XbaI) or distal (BstEII) positions.
[Strains used for panel A were DY682 (lanes 1-4), DY686 (lanes 5-8), DY684 (lanes 9-12), and
DY688 (13-16). Those for panel B were DY2900 (SEN1) and DY2902 (sen1E1597K
).] Strains
were grown at the indicated temperatures after 0 or 90 min of galactose induction and filters
were probed with the GAL1 or SED1 probes as indicated.
Figure 5- The effect of spacing upon start site selection. A) Start site mapping of IMD2 with
increasing spacing between the ‘high-guanine’ and ‘low-guanine’ (MPA) starts. An rrp6F strain
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was transformed with a family of plasmids containing increasing amounts of lambda DNA
inserted into the engineered BsiWI site (boxed in Fig. 1) between the high G and low G start
sites. Each derived strain was grown in the presence of 0.5 mM guanine for 30 min or 15 og/ml
MPA for 2 h before RNA was prepared and subjected to 5’-end mapping by primer extension.
[Strains used were DY1701 (lanes 1 & 2), DY1702 (lanes 3 & 4), DY1703 (lanes 5 & 6),
DY1704 (lanes 7 & 8), DY1706 (lanes 9 & 10), DY1707 (lanes 11 & 12), and DY1708 (lanes 13
& 14).] Extension products representing the low-guanine/downstream and high
guanine/upstream starts are indicated. Phosphorimaging was used to quantify the extension
product corresponding to the MPA-induced start and plotted as a function of the length of DNA
inserted between the two starts. Prism 4.0 (GraphPad Software, Inc.) was used for curve fitting.
B) Northern blot of IMD2 transcripts with increasing spacing between the ‘high-guanine’ and
‘low-guanine’ starts. The RNAs from strains described in part A were analyzed by northern
blotting. Strains DY1700 (lanes 1-3), DY1701 (lanes 4-6), DY1702 (lanes 7-9), DY1703 (10-
12), DY1704 (lanes 13-15), DY1706 (lanes 16-18), DY1707 (lanes 19-21), and DY1708 (lanes
22-24) were grown in SC-ura with 0.5 mM guanine and 15 og/ml MPA for 2 h before RNA was
prepared. Filters were probed with the ‘upstream’ or ‘downstream’ probes described in
Materials & Methods. C) Cultures from the strains in part B were set to an O.D.600nm of 0.01,
serially diluted in four-fold increments, and 5 ol of each dilution was spotted onto SC–ura and
SC–ura containing 15 og/ml MPA and grown at 30ºC.
Figure 6- Effect of Rpb9 subunit on initiation site selection. A) Start site mapping. RNA
transcribed from the native chromosomal loci was analyzed by northern blotting from strains
deleted for RRP6, RPB9, or both genes, as indicated in the figure. Strains DY1549 (lanes 1-3),
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YSC1021-551682 (lanes 4-6), and BY4741-4437 (lanes 7-9) were grown in the presence of 0.5
mM guanine for 30 min or 15 og/ml mycophenolic acid for 2 h before RNA was isolated for
primer extension. In “-“ lanes cells received neither treatment. The fast moving band in all lanes
is a non-specific species in the probe preparation that serves as an internal standard. B)
Northern analysis. RNA from strains BY4741-4437 (lanes 1-3), YSC1021-551682 (lanes 4-6),
and DY1549 (lanes 7-9) were prepared as in part A and subjected to northern blotting. The
upper panel of the northern blot was probed with the ‘upstream’ probe described in Materials and
Methods and the lower panel with the SED1 probe as a loading control.
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TABLE I. Yeast strains used in this study
Strain Genotype
46a1
MATa cup1F ura3 his3 trp1 lys2 ade2 leu2
BY47412
MATa his3Ä1 leu2Ä0 met15Ä0 ura3Ä0
BY4741-
44372
MATa his3Ä1 leu2Ä0 met15Ä0 ura3Ä0 rpb9F0
DY682 MATa cup1F ura3 his3 trp1 lys2 ade2 leu2 [pREF-XbaLuc (URA3)]
DY684 MATa cup1F ura3 his3 trp1 lys2 ade2 leu2 [pREF-BstLuc (URA3)]
DY686 MATa cup1F ura3 his3 trp1 lys2 ade2 leu2 sen1E1597K [pREF-XbaLuc (URA3)]
DY688 MATa cup1F ura3 his3 trp1 lys2 ade2 leu2 sen1E1597K [pREF-BstLuc (URA3)]
DY1035 MATa his3Ä1 leu2Ä0 met15Ä0 ura3Ä0 [pGalLuc (URA3)]
DY1038 MATa his3Ä1 leu2Ä0 met15Ä0 ura3Ä0 [pGalREF-XbaLuc (URA3)]
DY1400 MATa his3Ä1 leu2Ä0 met15Ä0 rrp6Ä0 ura3Ä0 [pGalLuc (URA3)]
DY1403 MATa his3Ä1 leu2Ä0 met15Ä0 rrp6Ä0 ura3Ä0 [pGalREF-XbaLuc (URA3)]
DY1532 MATa his3Ä1 leu2Ä0 met15Ä0 ura3Ä0 [pCYC1TT-F-XbaLuc (URA3)]
DY1534 MATa his3Ä1 leu2Ä0 met15Ä0 ura3Ä0 rrp6Ä0 [pCYC1TT-F-XbaLuc (URA3)]
DY1549 MATa his3Ä1 leu2Ä0 met15Ä0 ura3Ä0 rpb9F0 rrp6::URA3
DY1550 MATa his3Ä1 leu2Ä0 met15Ä0 ura3Ä0 [pChimera1-F-XbaLuc (URA3)]
DY1551 MATa his3Ä1 leu2Ä0 met15Ä0 ura3Ä0 rrp6Ä0 [pChimera1-F-XbaLuc (URA3)]
DY1552 MATa his3Ä1 leu2Ä0 met15Ä0 ura3Ä0 [pChimera1-R-XbaLuc (URA3)]
DY1554 MATa his3Ä1 leu2Ä0 met15Ä0 ura3Ä0 [pChimera-F-BsiLuc (URA3)]
DY1555 MATa his3Ä1 leu2Ä0 met15Ä0 ura3Ä0 rrp6Ä0 [pChimera-F-BsiLuc (URA3)]DY1558 MATa his3Ä1 leu2Ä0 met15Ä0 ura3Ä0 [pCYC1TT-F-BsiLuc (URA3)]
DY1559 MATa his3Ä1 leu2Ä0 met15Ä0 ura3Ä0 rrp6Ä0 [pCYC1TT-F-BsiLuc (URA3)]
DY1562 MATa his3Ä1 leu2Ä0 met15Ä0 ura3Ä0 [pGalNabMutXba-F-Luc]
DY1563 MATa his3Ä1 leu2Ä0 met15Ä0 ura3Ä0 rrp6Ä0 [pGalNabMutXba-F-Luc]
DY1700 MATa his3Ä1 leu2Ä0 met15F0 rrp6F0 ura3Ä0 imd2::LEU2 [pRS316-IMD2 (URA3)]
DY1701 MATa his3Ä1 leu2Ä0 met15F0 rrp6F0 ura3Ä0 imd2::LEU2 [pRS316-IMD2-BsiWImut(URA3)]
DY1702 MATa his3Ä1 leu2Ä0 met15F0 rrp6F0 ura3Ä0 imd2:: LEU2 [pRS316-IMD2-24bpn(URA3)]
DY1703 MATa his3Ä1 leu2Ä0 met15F0 rrp6F0 ura3Ä0 imd2:: LEU2 [pRS316-IMD2-36bpn(URA3)]
DY1704 MATa his3Ä1 leu2Ä0 met15F0 rrp6F0 ura3Ä0 imd2:: LEU2 [pRS316-IMD2-45bpn(URA3)]
DY1706 MATa his3Ä1 leu2Ä0 met15F0 rrp6F0 ura3Ä0 imd2:: LEU2 [pRS316-IMD2-103bpn(URA3)]
DY1707 MATa his3Ä1 leu2Ä0 met15F0 rrp6F0 ura3Ä0 imd2:: LEU2 [pRS316-IMD2-153bpn(URA3)]
DY1708 MATa his3Ä1 leu2Ä0 met15F0 rrp6F0 ura3Ä0 imd2:: LEU2 [pRS316-IMD2-218bpn(URA3)]
DY2900 MATa cup1Ä ura3 his3 trp1 lys2 ade2 leu2 [pCYC1TTF-XbaLuc (URA3)]
DY2902 MATa cup1Ä ura3 his3 trp1 lys2 ade2 leu2 sen1E1597K [pCYC1TTF-XbaLuc (URA3)]
Sen1E1597K1
MATa cup1Ä ura3 his3 trp1 lys2 ade2 leu2 sen1E1597K
YSC1021-
5516823
MATa his3Ä1 leu2Ä0 met15Ä0 ura3Ä0 rrp6F0
1 from D. Brow (U. Wisconsin, Madison)
2 from Research Genetics, Inc.
3 from Open Biosystems, Inc.
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Frrp6 Frrp6 Frrp6
no insert
RRP6 RRP6 RRP6
IMD2-IT CYC-TT
0 30 90 0 30 90 0 30 90 0 30 90 0 30 90 0 30 90
GAL1
XbaI
IMD2-IT or CYC-TT
FULL
SED1
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18
GAL1-IT
Galactose (min):
short RNA
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1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18
SED1
Frrp6 Frrp6 Frrp6RRP6 RRP6 RRP6
IMD2-IT
0 30 90 0 30 90 0 30 90 0 30 90 0 30 90 0 30 90
CYC-TTchimeric IT-CYC
M
GAL1-IT
SED1
GAL1-IT
1 2 3 4 5 6 7 8 9 10 11 12
GAL1
XbaI
terminator
A
B
GAL1
BsiWI
terminator
Frrp6 Frrp6RRP6 RRP60 30 90 0 30 90 0 30 90 0 30 90
CYC-TTchimeric IT-CYC
FULL
Galactose (min):
Galactose (min):
short
short
BsiWI
XbaI
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AGUUUCUU0 30 90 0 30 90 0 30 90 0 30 90 M
Frrp6RRP6
Galactose (min):
GAL1-IT
FULL
short
RNA sequence: AGUUUCUU
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SEN1SEN1 sen1E1597Ksen1E1597K
25� 25� 25� 25�37� 37� 37� 37�
0galactose (min):
SED1
GAL1-IT
1 2 3 4 5 6 7 8 9 10 11 12 13 1415
GAL1
XbaI
IMD2-IT or
BstEII
IMD2-IT
FULL
16
0 00 0 0 0 090 90 90 90 90 90 90 90
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SEN1 sen1E1597K
25� 25�37� 37�
Galactose:
SED1
GAL1-CYCTT
00 0 030 30 30 3090 90 90 90
1 2 3 4 5 6 7 8 9 10 11 12
GAL1
XbaI
CYC-TT
FULL
BstEII
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upstream
starts
low G
(MPA) start
1 2 3 4 5 6 7 8 910 1112 1314
0 100 2000
5000
10000
15000
bp inserted DNA
MP
A in
itia
tio
n s
ite
(ph
osp
ho
rim
ag
er
un
its)
+ guanine:
+ MPA: ++-
-+
+-
-+
+-
-+
+-
-+
+-
-+
+-
-+
+-
-
bp inserted: 0 24 36 45 103 153 218
AG
GG
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+ guanine:
+ MPA:
bp inserted: 0 (Bsi) 24 36 45 103 153 218
+- -+- - +- -+- - +- -+- - +- -+- -+- - +- - +- - +- -+- - +- -
0 (wt)
+- -+- -
upstreamprobe
downstreamprobe
1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 23 24
FULL
FULL
short
short
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SC-ura+15µg/ml MPASC-ura
IMD2 WT
IMD2 BsiWI
24 bp insert
36 bp insert
45 bp insert
103 bp insert
153 bp insert
218 bp insert
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rpb9Frrp6F
RPB9
rrp6Frpb9FRRP6
[+
guanin
e
+guanin
e
+guanin
e
- - -
+M
PA
+M
PA
+M
PA
“low G” start
“high G” starts
1 2 3 4 5 6 7 8 9
AG
GGACCEPTED
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Frrp6 RPB9 RRP6 Frpb9 Frrp6 Frpb9
guanine:
MPA: +--
--+
-+-
-+
-- +-
SED1
IMD2 mRNA
1 2 3 4 5 6 7 8 9
+- -
shortACCEPTED on A
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