Top Banner
REVIEW SESSION Wednesday, September 15 5:30 5:30 PM PM SHANTZ 242 E SHANTZ 242 E
33

REVIEW SESSION 5:30 PM Wednesday, September 15 5:30 PM SHANTZ 242 E.

Jan 05, 2016

Download

Documents

Poppy Fleming
Welcome message from author
This document is posted to help you gain knowledge. Please leave a comment to let me know what you think about it! Share it to your friends and learn new things together.
Transcript
Page 1: REVIEW SESSION 5:30 PM Wednesday, September 15 5:30 PM SHANTZ 242 E.

REVIEW SESSION

Wednesday, September 15 5:30 PM5:30 PM

SHANTZ 242 ESHANTZ 242 E

Page 2: REVIEW SESSION 5:30 PM Wednesday, September 15 5:30 PM SHANTZ 242 E.

Gene Regulation

Page 3: REVIEW SESSION 5:30 PM Wednesday, September 15 5:30 PM SHANTZ 242 E.

Gene Regulation

Gene expression can be turned on, turned off, turned up or turned down!

For example, as test time approaches, some of you may note that stomach acid production increases dramatically…. due to regulation of the genes that control synthesis of HCl by cells within the gastric pits of the stomach lining.

Page 4: REVIEW SESSION 5:30 PM Wednesday, September 15 5:30 PM SHANTZ 242 E.

Gene Regulation in Prokaryotes

Prokaryotes may turn genes on and off depending on metabolic demands and requirements for

respective gene products.

NOTE: For prokaryotes, “turning on/off” refers almost exclusively to stimulating or repressing

transcription

Page 5: REVIEW SESSION 5:30 PM Wednesday, September 15 5:30 PM SHANTZ 242 E.

Gene Regulation in Prokaryotes

Inducible/Repressible Inducible/Repressible gene products: those produced only when specific chemical substrates are present/absent.

ConstitutiveConstitutive gene products: those produced continuously, regardless of chemical substrates present.

Page 6: REVIEW SESSION 5:30 PM Wednesday, September 15 5:30 PM SHANTZ 242 E.

Gene Regulation in Prokaryotes

Regulation may be

Negative: gene expression occurs unless it is shut off by a regulator molecule

or

Positive: gene expression only occurs when a regulator mole turns it on

Page 7: REVIEW SESSION 5:30 PM Wednesday, September 15 5:30 PM SHANTZ 242 E.

Operons

In prokaryotes, genes that code for enzymes all related to a single metabolic process tend to be organized into clusters within the genome, called operonsoperons.

An operon is usually controlled by a single regulatory unit.

Page 8: REVIEW SESSION 5:30 PM Wednesday, September 15 5:30 PM SHANTZ 242 E.

Regulatory Elements

ciscis-acting element-acting element: The regulatory region of the DNA that binds the molecules that influences expression of the genes in the operon. It is almost always upstream (5’) to the genes in the operon.

Trans-acting elementTrans-acting element: The molecule(s) that interact with the cis-element and influence expression of the genes in the operon.

Page 9: REVIEW SESSION 5:30 PM Wednesday, September 15 5:30 PM SHANTZ 242 E.

The lac operonThe lac operon contains the genes that must be

expressed if the bacteria is to use the disaccharide lactose as the primary energy source.

To be used as an energy source, lactose must be cleaved into glucose and galactose. The glucose is then available for metabolism (glycolysis).

Note: glucose is the preferred energy substrate.

Page 10: REVIEW SESSION 5:30 PM Wednesday, September 15 5:30 PM SHANTZ 242 E.

Negative Control

The genes in the lac operon are normally turned off, and only expressed when a repressor molecule is removed from the regulatory region.

This repressor is removed only in the presence of lactose

Page 11: REVIEW SESSION 5:30 PM Wednesday, September 15 5:30 PM SHANTZ 242 E.

LacI P O lacAlacYlacZ

The lac Operon

Repressorgene

Regulatory Region Structural Genes

P=PromoterO=Operator

Page 12: REVIEW SESSION 5:30 PM Wednesday, September 15 5:30 PM SHANTZ 242 E.

Structural GenesStructural genes are those that encode for the

enzymes that do the metabolic work.

LacZ: -galactosidase, cleaves lactose into glucose and galactose

LacY: Permease, promotes entry of lactose into cell

LacA: Transacetylase, thought to reduce toxicity of byproducts of lactose metabolism

Page 13: REVIEW SESSION 5:30 PM Wednesday, September 15 5:30 PM SHANTZ 242 E.

Structural Genes

In prokaryotes, all the structural genes within an operon are usually transcribed as a single mRNA, then the genes are independently translated by ribosomes.

Page 14: REVIEW SESSION 5:30 PM Wednesday, September 15 5:30 PM SHANTZ 242 E.

LacI—The Repressor

LacI is the regulatory molecule.

When there is no lactose present in the cell,LacI binds to the Operator element and blocks binding of RNA polymerase to the Promoter element.

LacI P O lacAlacYlacZX

Page 15: REVIEW SESSION 5:30 PM Wednesday, September 15 5:30 PM SHANTZ 242 E.

LacI—The Repressor

When lactose IS present, the genes to metabolize lactose must be expressed.

Lactose itself causes LacI to dissociate from the operator, which frees up the promoter region, allowing RNA polymerase to bind, and transcription begins.

Lactose is the inducer moleculeinducer molecule for the lac operon.

Page 16: REVIEW SESSION 5:30 PM Wednesday, September 15 5:30 PM SHANTZ 242 E.

Induction of the lac operon

LactoseBinding of lactose causes achange in the shape of LacI

LacI P O lacAlacYlacZ

Page 17: REVIEW SESSION 5:30 PM Wednesday, September 15 5:30 PM SHANTZ 242 E.

Induction of the lac operon

LacI P O lacAlacYlacZ

LacI P O lacAlacYlacZ

Page 18: REVIEW SESSION 5:30 PM Wednesday, September 15 5:30 PM SHANTZ 242 E.

What happens if you mutate LacI?

LacI encodes the lac repressor, which keeps the operon shut off in the absence of lactose.

Page 19: REVIEW SESSION 5:30 PM Wednesday, September 15 5:30 PM SHANTZ 242 E.

What happens if you mutate LacI?

Inactivation of LacI would be called a constitutive constitutive mutationmutation, because the genes of the lac operon would be on all the time even if there is no lactose present (removed repression).

Page 20: REVIEW SESSION 5:30 PM Wednesday, September 15 5:30 PM SHANTZ 242 E.

Positive Control of the lac Operon

A further increase in transcription of the lac operon occurs if a molecule called catabolite-activating protein (CAP)(CAP) also binds the promoter region.

LacI P O lacAlacYlacZ

CAP facilitates the binding of RNA polymerase,and therefore increases transcription

Page 21: REVIEW SESSION 5:30 PM Wednesday, September 15 5:30 PM SHANTZ 242 E.

Positive Control

Remember, glucose is the preferred substrate.

CAP exists in the state that will bind the promoter ONLY when glucose is absent.

LacI P O lacAlacYlacZ

This is the form CAP takes when there is no glucose

Page 22: REVIEW SESSION 5:30 PM Wednesday, September 15 5:30 PM SHANTZ 242 E.

Positive Control

When glucose is present, CAP exists in a state that will NOT bind the promoter of the lac operon.

LacI P O lacAlacYlacZ

XThis is the shape CAP takes when glucose ispresent. It cannot bind the promoter in this shape

X

Page 23: REVIEW SESSION 5:30 PM Wednesday, September 15 5:30 PM SHANTZ 242 E.

Regulation of the lac Operon

So, transcription is regulated as follows:

OffOff when lactose is absent (repressed)

ActiveActive when lactose is present as well as glucose (de-repressed)

Really activeReally active when lactose is present but glucose is absent (activated)

Page 24: REVIEW SESSION 5:30 PM Wednesday, September 15 5:30 PM SHANTZ 242 E.

Gene Regulation in Eukaryotes

Page 25: REVIEW SESSION 5:30 PM Wednesday, September 15 5:30 PM SHANTZ 242 E.

Differences between Prokaryotes and Eukaryotes

1. DNA is a lot more complicated in eukaryotes—there’s a lot more of it and it’s complexed with proteins to form chromatin

2. Genetic information is carried on multiple chromosomes

3. Transcription and translation are physically separated

Page 26: REVIEW SESSION 5:30 PM Wednesday, September 15 5:30 PM SHANTZ 242 E.

Differences between Prokaryotes and Eukaryotes (cont.)

4. Eukaryotic mRNA is processed prior to translation

5. Eukaryotic mRNA is much more stable (not as easily degraded)

Gene expression can be controlled at the level of translation!

6. Different cell types express different genes

Page 27: REVIEW SESSION 5:30 PM Wednesday, September 15 5:30 PM SHANTZ 242 E.

Chromatin Remodeling

Chemical alteration of the histone proteins of chromatin facilitates or inhibits access of RNA polymerases to DNA promoters.

Page 28: REVIEW SESSION 5:30 PM Wednesday, September 15 5:30 PM SHANTZ 242 E.

Recruitment of Co-activators

Remember enhancer elementsenhancer elements? These are binding sites for molecules that influence formation of the RNA polymerase initiation complex.

Enhancer elements may have DNA sequences for both positive and negative regulators of transcription.

Page 29: REVIEW SESSION 5:30 PM Wednesday, September 15 5:30 PM SHANTZ 242 E.

Enhancers

The presence or absence of regulators is determined by the cell’s environment, metabolic state, developmental state and/or the presence or absence of signal molecules.

The net effect of all the information available, summed up by the regulators present, dictates the transcription efficiency of RNA polymerase from a given promoter.

Page 30: REVIEW SESSION 5:30 PM Wednesday, September 15 5:30 PM SHANTZ 242 E.

DNA Methylation

Chemical modification of DNA by adding or removing methyl (-CH3) groups from the DNA bases, usually cytosine.

The presence of the methyl group alters the shape of DNA, which influences the binding of proteins to the methylated DNA.

Page 31: REVIEW SESSION 5:30 PM Wednesday, September 15 5:30 PM SHANTZ 242 E.

DNA Methylation

Typically, increased methylation decreases transcription efficiency.

In mammalian females, one X chromosome is inactivated (only one of the X chromosomes is used to drive transcription). The inactivated X chromosome has much more methylation than the active chromosome.

Page 32: REVIEW SESSION 5:30 PM Wednesday, September 15 5:30 PM SHANTZ 242 E.

Post-Transcriptional Regulation

Alternative Splicing:

Exon 1 Exon 2 Exon 3 Exon 4 Exon 5

Exon 1 Exon 2 Exon 3 Exon 4 Exon 5

Exon 1 Exon 2 Exon 4 Exon 5

1.

2.

Page 33: REVIEW SESSION 5:30 PM Wednesday, September 15 5:30 PM SHANTZ 242 E.

Post-Transcriptional Control

RNA Stability

1. Stability sequences

2. Instability sequences

3. Translation efficiency—increased translation increases stability