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Regulation of Gene Expression

Regulation of Gene Expression. Dr. Ishtiaq Ahmad Khan Dr. Panjwani Center for Molecular Medicine and Drug Research. Definitions. Constitutively expressed genes:

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Regulation of Gene Expression

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  1. Regulation of Gene Expression Dr. Ishtiaq Ahmad Khan Dr. Panjwani Center for Molecular Medicine and Drug Research

  2. Definitions • Constitutively expressed genes: • Genes that are actively transcribed (and translated) under all experimental conditions, at essentially all developmental stages, or in virtually all cells. • Inducible genes: • Genes that are transcribed and translated at higher levels in response to an inducing factor • Repressible genes: • Genes whose transcription and translation decreases in response to a repressing signal

  3. Definitions • Housekeeping genes: • genes for enzymes of central metabolic pathways (e.g. TCA cycle) • these genes are constitutively expressed • the level of gene expression may vary

  4. Modulators of transcription • Modulators: (1) specificity factors, (2) repressors, (3) activators • Specificity factors: Alter the specificity of RNA polymerase Examples: s-factors (s70, s32 ), TBPs s70 s32 Standard promoter Heat shock promoter Housekeeping gene Heat shock gene

  5. Modulators of transcription 2. Repressors: mediate negative gene regulation may impede access of RNA polymerase to the promoter actively block transcription bind to specific “operator” sequences (repressor binding sites) Repressor binding is modulated by specific effectors Effector (e.g. endproduct) Repressor Operator Coding sequence Promoter

  6. Negative regulation (1) Repressor Effector Example: lac operon RESULT: Transcription occurs when the gene is derepressed Source: Lehninger pg. 1076

  7. Negative regulation (2) Repressor Effector (= co-repressor) Example: pur-repressor in E. coli; regulates transcription of genes involved in nucleotide metabolism Source: Lehninger pg. 1076

  8. Modulators of transcription 3. Activators: mediate positive gene regulation bind to specific regulatory DNA sequences (e.g. enhancers) enhance the RNA polymerase -promoter interaction and actively stimulate transcription common in eukaryotes RNA pol. Activator promoter Coding sequence

  9. Positive regulation (1) Activator RNA polymerase Source: Lehninger pg. 1076

  10. Positive regulation (2) Activator Effector RNA polymerase Source: Lehninger pg. 1076

  11. Operons • a promoter plus a set of adjacent genes whose gene products function together. • usually contain 2 –6 genes, (up to 20 genes) • these genes are transcribed as a polycistronic transcript. • relatively common in prokaryotes • rare in eukaryotes

  12. Pi I P O1 Z Y A O3 O2 The lactose (lac) operon • Contains several elements • lacZ gene = b-galactosidase • lacY gene = galactosidase permease • lacA gene = thiogalactoside transacetylase • lacI gene = lac repressor • Pi = promoter for the lacI gene • P = promoter for lac-operon • O1 = main operator • O2 and O3 = secondary operator sites (pseudo-operators)

  13. The lac operon consists of three structural genes, and a promoter, a terminator,regulator, and an operator. The three structural genes are: lacZ, lacY, and lacA. • lacZ encodesβ-galactosidase (LacZ), an intracellular enzyme that cleaves the disaccharide lactose into glucose and galactose. • lacY encodesβ-galactoside permease (LacY), a membrane-bound transport protein that pumps lactose into the cell. • lacA encodesβ-galactoside transacetylase (LacA), an enzyme that transfers an acetyl group from acetyl-CoA to β-galactosides. • Only lacZ and lacY appear to be necessary for lactose catabolism.

  14. First Level • The lacI gene coding for the repressor lies nearby the lac operon and is always expressed (constitutive). • Hinder production of β-galactosidase in the absence of lactose. • If lactose is missing from the growth medium, the repressor binds very tightly to a short DNA sequence called the lac operator. • The repressor binding to the operator interferes with binding of RNA Pol to the promoter, and therefore mRNA encoding LacZ and LacY is only made at very low levels. • When cells are grown in the presence of lactose, however, a lactose metabolite called allolactose , which is a combination of glucose and galactose, binds to the repressor, causing a change in its shape. • Thus altered, the repressor is unable to bind to the operator, allowing RNAP to transcribe the lac genes and thereby leading to higher levels of the encoded proteins.

  15. Second Level • The second control mechanism is a response to glucose, which uses the Catabolite activator protein (CAP) to greatly increase production of β-galactosidase  in the absence of glucose.  • Cyclic adenosine monophosphate  (cAMP) is a signal molecule whose prevalence is inversely proportional to that of glucose. • It binds to the CAP, which in turn allows the CAP to bind to the CAP binding site (a 16 bp DNA sequence upstream of the promoter), • which assists the RNAP in binding to the DNA. In the absence of glucose, the cAMP concentration is high and binding of CAP-cAMP to the DNA significantly increases the production of β-galactosidase • enabling the cell to hydrolyse (digest) lactose and release galactose and glucose.

  16. LacZ LacY LacA Inducer molecules: Allolactose: - natural inducer, degradable IPTG (Isopropylthiogalactoside) - synthetic inducer, not metabolized, lacI repressor Pi Pi I I P P Q1 Q1 Z Z Y Y A A Q3 Q3 Q2 Q2 Regulation of the lac operon

  17. Operons in eukaryotes • Dicistronic transcription units specify a messenger RNA (mRNA) encoding two separate genes that is transported to the cytoplasm and translated in that form. Presumably, internal ribosome entry sites (IRES), or some form of translational re-initiation following the stop codon, are responsible for allowing translation of the downstream gene. • In the other type, the initial transcript is processed by 3΄ end cleavage and trans-splicing to create monocistronic mRNAs that are transported to the cytoplasm and translated. • Like bacterial operons, eukaryotic operons often result in co-expression of functionally related proteins. Blumenthal T, BRIEFINGS IN FUNCTIONAL GENOMICS AND PROTEOMICS. VOL 3. NO 3. 199–211. NOVEMBER 2004

  18. Genes whose function is to specify mitochondrial proteins and those that encode the basic machinery for gene expression, transcription, splicing and translation have a very strong tendency to be transcribed in operons

  19. Examples in C. elegans • An operon that expresses two subunits of the acetylcholine receptor. • An operon that encodes two proteins needed for modifying collagen, expressed only in collagen-producing cells. • An operon that co-expresses an ion channel protein with a protein that modifies the activity of that channel;

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