the replication of dna generalprinciples-bidirectional, semi ... · replication in prokaryotes and...
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The Replication of DNAGeneral principles - bidirectional,semi-conservative and semi-discontinuous replication.Replication in prokaryotes andeukaryotes.
Unit III
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DNA Replication
Before cells divide, they must double their DNA so that each cell gets identical copies of the DNA strands.
DNA replication helps assure that the bases are copied correctly.
Enzymes carry out the process.
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Overview of DNAreplicationThe hydrogen bondsbreak to “unzip” theDNA strand. Enzymesguide free nucleotidesto the exposed singlestrands and match thenucleotides.
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Meselson and Stahl experiment (1957)
• Bacteria were grown in a medium containingnitrogen 15 for several generations
• If the medium contains no other nitrogen source, E.coli will use N15 and incorporate it into their DNA
• Eventually they will only have N15• Once the E. coli had only N15, they were put into a
growing medium containing N14• N15 is heavier than N14 making new incorporation
of nitrogen easy to distinguish• The differences were measured according to the
densities of the new strand
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How exactly does DNA replicate?
Findings:
– Replication is carried out by DNA polymerase.
• 50 nucleotides per second in mammals
• 500 nucleotides per second in bacteria
– DNA strands unzip and each one acts as a template for
the formation of a new strand.
– Nucleotides line up along template strand in accordance
with base pairing rules.
– Enzymes link the nucleotides together to form new DNA
strands.
– Semiconservative replication: Each new helix will
contain one new strand and one old strand.
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DNA Replication is Semiconservative
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How exactly does DNA replicate?
– Strands are antiparallel: Run in opposite directions.
– DNA polymerases can only add nucleotides to one
end of the strand (3’ end).
– New strands grow in a 5’ to 3’ direction
– Replication fork with:
• Leading strand: Made continuously.
• Lagging strand: Made discontinuously in Okazaki
fragments which are then joined together.
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Transcription & Modification of RNAConcept of Central Dogma: Basic concepts oftranscription in prokaryotes and eukaryotes.Principles of transcriptional regulation; Prokaryotes:Regulation of lactose metabolism and tryptophansynthesis in E. coli; Eukaryotes: transcriptionfactors; Split genes, introns and exons, mRNAtransport.
Unit IV
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Basic concept of transcription
Prokaryotic cell
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Eukaryotic cell
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Transcription vs. Translation
DNA RNA Proteins
Transcription:• Like copying information from a
book in the reserved section of the library
• Using the same language
Translation:• Literally translating between
two different languages
• Take the copied info from the library and translate it into Hindi/French/Spanish
नम�कार
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enzymatic
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“Upstream” of the gene is a promoter• whole promoter = several dozen nucleotides
example of DNA that is essential but is not transcribed
where the gene is
the “start here” signal
Transcription Unit:
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Elongation
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GC rich regions capable of making hairpin structure
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Some terminators require a rho factor fortermination and is called as rho dependenttermination.
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2α, β, β’
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(α)
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Promoter sequence
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Enhancers
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Key Concepts of gene regulation
• Several strategies are used to regulategene expression
• Many prokaryotic genes are regulated inoperons
• Eukaryotic genes are regulated bytranscription factors and DNA changes
• Eukaryotic gene expression can beregulated after transcription
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1. Transcription2. Post-transcriptional
modification (Splicing)3. Translation4. Post-translational
modification of protein
Several steps in the gene expression processmay be modulated, including the
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Transcriptional regulation/Consequences due to mutation in transcription factors
• Predominant form ofregulation of geneexpression found in cells.
• The protein factors thatregulate gene expressionvia transcription arecritical to many biologicalprocesses.
• When these factorsfunction incorrectly,pathological and otheraberrant effects occur.
Development of the eye in humans
Wing development in flies
Flower development in plants
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Classification of genes with respect to their expression
Constitutive (house keeping) genes:Expressed at a fix rate irrespective to thecell condition or environmental cue.
Controllable genes:Are expressed only as needed.Their amount may increase or decreasewith respect to basal level expression.
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Regulation of gene expression may be categorized in to two types;
1.Positive regulation (Inducible genes)Genes are turned on
2. Negative regulation (Repressive genes)Genes are turned off
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1. Positive regulation When the expression of a gene is quantitatively
increased by the presence of specific regulatoryelement, then it is known as positive regulation
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2. Negative regulation When the expression of a gene is quantitatively
decreased by the presence of specific regulatoryelement, then it is known as negative regulation
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Bacterial gene regulation
• Francois Jacob and Jacques Monod (1961) were the first to propose the operon model of gene regulation following genetic analysis of E. coli
• Operon: In bacteria, the genes that encode the enzymes of a metabolic pathway are usually clustered together in units on the chromosome in a functional complex called an operon.
• A typical bacterial operon consists of:-• Structural genes• Promoter• Operator• Regulator
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• Our understanding of transcriptional regulation comes fromstudies of enzyme induction in E.coli.
• E. coli exhibit an extremely sophisticated regulation of enzymeinduction in response to changing environmental conditions.
• The primary source of food for bacteria is glucose!• If both glucose and lactose are present together, glucose is
utilized first.• The organism will first breakdown glucose by turning on genes
for enzymes that metabolize glucose.• The enzymes required for lactose metabolism are shut off!• Once the glucose is completely metabolized, the genes
responsible for glucose metabolism are shut down. Then thegenes for the enzymes involved in lactose metabolism areturned on.
How does a cell turn on and off these genes?
Lac operon
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Lac operon: The cluster of genes that regulates
production of the enzymes needed to degrade lactose inE. coli and some other enteric bacteria.
• Lactose is a disaccharidecomposed of glucose andgalactose.
• When only lactose is present, thegenes for lactose metabolism areturned on.
• When all the lactose is brokendown, the genes are shut off.
Lac operon: Regulatory response to lactose
• This uses an intracellular regulatory protein called as lactose repressor.
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When lactose is absent in the medium
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When lactose is present in the medium
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Lac operon: Regulatory response in presence of both glucose and lactose
• If both glucose and lactose are present together, glucose is utilized first. The mechanism by which bacteria prefers glucose over lactose is called as catabolite repression.
• It is not enough for lactose alone to be present to induce the lac operon.
• RNA polymerase affinity for the promoter of lac operon increases by a regulatory protein i.e. cAMPreceptor protein (CRP).
• Glucose inhibits the formation of cAMP.• High glucose conc. lowers the conc. of cAMP and
vice versa.
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CRP-cAMP complex controls lac operon
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Regulation of tryptophan synthesis in E. coli(The ‘Tryptophan’ Operon)
• trp operon – a repressible operon
• Normally, the structural genes (which are used tosynthesize tryptophan) for this operon, are operational.
• These genes are repressed when tryptophan isreadily available to the bacteria from the environment.
• A corepressor (tryptophan) binds to the repressor,altering its shape so that it binds to the operator regionof the DNA sequence.
• This then stops the transcription of the structural genesand tryptophan synthesis is halted.
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What type of feedback is demonstrated upon the structural genes in each “operon” case?
• lac operon demonstrates positive feedback
• trp operon demonstrates negative feedback
• May be inducible operons generally controlcatabolic pathways and repressible operonsusually control anabolic pathways.
What type of pathway do inducible operonsgenerally control:
Anabolic or Catabolic?
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