Table of contents
- 1. Introduction to Genetics51m
- 2. Mendel's Laws of Inheritance3h 37m
- 3. Extensions to Mendelian Inheritance2h 41m
- 4. Genetic Mapping and Linkage2h 28m
- 5. Genetics of Bacteria and Viruses1h 21m
- 6. Chromosomal Variation1h 48m
- 7. DNA and Chromosome Structure56m
- 8. DNA Replication1h 10m
- 9. Mitosis and Meiosis1h 34m
- 10. Transcription1h 0m
- 11. Translation58m
- 12. Gene Regulation in Prokaryotes1h 19m
- 13. Gene Regulation in Eukaryotes44m
- 14. Genetic Control of Development44m
- 15. Genomes and Genomics1h 50m
- 16. Transposable Elements47m
- 17. Mutation, Repair, and Recombination1h 6m
- 18. Molecular Genetic Tools19m
- 19. Cancer Genetics29m
- 20. Quantitative Genetics1h 26m
- 21. Population Genetics50m
- 22. Evolutionary Genetics29m
13. Gene Regulation in Eukaryotes
GAL Regulation
Problem 25a
Textbook Question
Regulation of the lac operon in E. coli (see Chapter 16) and regulation of the GAL system in yeast are analogous in that they both serve to adapt cells to growth on different carbon sources. However, the transcriptional changes are accomplished very differently. Consider the conceptual similarities and differences as you address the following.
Compare and contrast how these two systems are negatively regulated such that they are downregulated in the presence of glucose.
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<span>Identify the key components involved in the regulation of the lac operon in E. coli and the GAL system in yeast.</span>
<span>Understand the mechanism of negative regulation in the lac operon: In the presence of glucose, the lac operon is downregulated through catabolite repression, where glucose decreases the levels of cyclic AMP (cAMP), reducing the activity of the cAMP receptor protein (CRP), which is necessary for the activation of the lac operon.</span>
<span>Examine the negative regulation of the GAL system in yeast: In the presence of glucose, the GAL genes are downregulated by the Mig1 protein, which is a repressor that binds to the promoters of GAL genes and recruits a complex that modifies chromatin to repress transcription.</span>
<span>Compare the role of glucose in both systems: In both E. coli and yeast, glucose acts as a preferred carbon source and its presence leads to the downregulation of alternative metabolic pathways (lactose in E. coli and galactose in yeast) through different molecular mechanisms.</span>
<span>Contrast the molecular mechanisms: The lac operon uses a reduction in cAMP levels to prevent activation, while the GAL system uses a repressor protein (Mig1) to directly inhibit transcription.</span>
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Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Lac Operon Regulation
The lac operon in E. coli is a classic example of gene regulation, where the presence of lactose induces the expression of genes necessary for lactose metabolism. In the absence of lactose, a repressor protein binds to the operator region, preventing transcription. When glucose is present, the operon is further downregulated through catabolite repression, where high glucose levels inhibit the production of cyclic AMP (cAMP), reducing the activity of the cAMP-CAP complex that promotes transcription.
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Lac Operon Regulation
GAL System Regulation
The GAL system in yeast regulates the metabolism of galactose and is controlled by a different mechanism. When glucose is abundant, the GAL genes are repressed through a process called glucose repression, which involves the inhibition of transcription factors necessary for GAL gene expression. This repression occurs via the Snf1 kinase pathway, which is activated in low glucose conditions, allowing the transcription of GAL genes when glucose is scarce.
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GAL Regulation
Catabolite Repression
Catabolite repression is a regulatory mechanism that ensures cells preferentially utilize the most efficient carbon source, typically glucose. In both the lac operon and the GAL system, the presence of glucose leads to a decrease in the expression of genes involved in the metabolism of alternative sugars. This is achieved through the reduction of cAMP levels in E. coli and the activation of specific repression pathways in yeast, highlighting a common strategy in different organisms to optimize energy use.
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