centromeres

47

Upload: hector

Post on 23-Mar-2016

24 views

Category:

Documents


0 download

DESCRIPTION

Centromeres. Heterochromatin Kinetochore - spindle fiber attachment No universal DNA sequences Repeat sequences - CENs - 5 to 170 bp – humans, alphoid satellite repeats Specific associated proteins. Telomeres. Telomeres. About 15,000 bp in humans Lagging strand problem - PowerPoint PPT Presentation

TRANSCRIPT

Page 1: Centromeres
Page 2: Centromeres

Centromeres

Heterochromatin

Kinetochore - spindle fiber attachment

No universal DNA sequences

Repeat sequences - CENs - 5 to 170 bp – humans, alphoid satellite repeats

Specific associated proteins

Page 3: Centromeres
Page 4: Centromeres

Telomeres

Page 5: Centromeres
Page 6: Centromeres

Telomeres

•About 15,000 bp in humans•Lagging strand problem•Telomere shortening•Hayflick – and then we die•Cancer, AIDs, stem cells

Page 7: Centromeres

The structure and organization of chromosomes change during the course of the cell cycle.

Page 8: Centromeres
Page 9: Centromeres
Page 10: Centromeres
Page 11: Centromeres

Nonrandom chromosome positioning

• Gene rich chromosomes toward center• Gene poor chromosomes toward

periphery• Centromeres are not the determining

factor• Chromosomes with adjacent positions

more likely to interact cytolologically

Page 12: Centromeres

How porous are territories?

• Previously it was predicted that active genes would be located at the surface of chromosome territories.

• Now, it appears that they are also in the interior

• Some are also found on loops outside of the territory

Page 13: Centromeres
Page 14: Centromeres

In order for DNA to physically fit into a nucleus, several levels of packing are necessary.

How is the DNA packaged in this way and how is it available for replication and transcription if it is tightly packed?

Page 15: Centromeres

The 4 nm DNA filament

Page 16: Centromeres

Histones • folding and coiling chromosomes• 45% of the total mass• 60 million molecules of each type per cell

Page 17: Centromeres

• Histones are highly conserved across all eukaryotic organisms

• Histones are small basic proteins (102-135 aa) rich in lysine and arginine

• Each histone contains a region that folds in a characteristic structure called the histone fold and a tail region

• Tail region is post translationally modified in various ways to control many aspects of chromatin structure

Page 18: Centromeres
Page 19: Centromeres
Page 20: Centromeres
Page 21: Centromeres

Core particle - Approximately 1.8 turns of DNA (consisting of 146 bp) wound around the outside of the histone octamer.

Page 22: Centromeres

Note that other chromatin modifying complexes include kinases, methylases and ubiquitin conjugating proteins.

Acetylation typically correlates with transcriptional activation while deacetylation correlates with repression.

Page 23: Centromeres

Histone “tails” stick out between the coil of DNA

Post-translational chemical modification of the tails controls function. Modification patterns comprise the “histone code”.

Page 24: Centromeres
Page 25: Centromeres

• Non-histone proteins (NHPs, acidic proteins, nonhistone chromosomal proteins, NHC proteins)– help regulate DNA transcription and

replication– at least 30 types

Page 26: Centromeres

“Chromatin remodeling complexes” and “Chromatin modifying complexes” are important for transcriptional activation

Chromatin modifying complex

Page 27: Centromeres
Page 28: Centromeres
Page 29: Centromeres
Page 30: Centromeres

Chromatin decondensation appears to require two types of protein complexes each made of several polypeptide subunits:

1. Histone acetylase complexes.These are often referred to as HATS for histone

acetylases.

2. Chromatin remodeling factors. These are often refered to as Swi/Snf factors

because they were first identified as yeast mutants defective in mating type switching and in the ability to metabolize sucrose (sucrose non-fermenting).

Page 31: Centromeres

Chromatin remodeling factors use energy from ATP hydrolysis to rearrange the packing of nucleosomes in higher order chromatin structures

There are several different chromatin remodeling complexes in cells.

Some of these bind to activation domains andde-condense the associated chromatin.

Some bind to repression domains and condense the associated chromatin.

Page 32: Centromeres
Page 33: Centromeres
Page 34: Centromeres
Page 35: Centromeres

The 10 nm nucleoprotein fibril

Nucleosomes + 60 (approx) bp DNA

Page 36: Centromeres

A eukaryotic gene of 10,000 bp will be associated with about 50 nucleosomes. A human cell contains 3 x 107 nucleosomes.

One molecule of histone H1 and the nucleososome is sometimes referred to as the chromatosome.

Page 37: Centromeres

Most interphase chromatin is condensed into 30nm coils?

Page 38: Centromeres

A model for the structure of an interphase chromosome

Most interphase chromatin is condensed into 30nm coils?

Page 39: Centromeres

Lampbrush chromosomes (amphibian oocyte, immature eggs)

Page 40: Centromeres

In mitotic chromosomes, a scaffold is formed, and matrix attachment sites correspond to sites of chromatin attachment to the scaffold?

Page 41: Centromeres

Histone depleted metaphase chromosomes

Page 42: Centromeres
Page 43: Centromeres

Scaffold Attachment Regions (SARs)?

Regions of the chromosomes with sequences specific for topoisomerase, HMG protein, and histone H1 binding

Found only in untranscribed regions of the eukaryotic chromosomes

Spaced along the chromosomes, with the intervening regions containing one or more genes?

Highly AT rich (65%) and may be several hundred bp long

Page 44: Centromeres

Discrete loops of DNA appear to be connected at both ends to the scaffold

Page 45: Centromeres

Quaternary structure: final folding into chromosome shape

Page 46: Centromeres
Page 47: Centromeres