Textbook Question
What features of eukaryotes provide additional opportunities for the regulation of gene expression compared to bacteria?
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Ch. 16 - Regulation of Gene Expression in Eukaryotes
Klug10th EditionEssentials of GeneticsISBN: 9780135588789
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Table of contents
- Ch. 1 - Introduction to Genetics16
- Ch. 2 - Mitosis and Meiosis28
- Ch. 3 - Mendelian Genetics37
- Ch. 4 - Modification of Mendelian Ratios53
- Ch. 5 - Sex Determination and Sex Chromosomes32
- Ch. 6 - Chromosome Mutations: Variation in Number and Arrangement37
- Ch. 7 - Linkage and Chromosome Mapping in Eukaryotes36
- Ch. 8 - Genetic Analysis and Mapping in Bacteria and Bacteriophages24
- Ch. 9 - DNA Structure and Analysis38
- Ch. 10 - DNA Replication29
- Ch. 11 - Chromosome Structure and DNA Sequence Organization22
- Ch. 12 - The Genetic Code and Transcription36
- Ch. 13 - Translation and Proteins27
- Ch. 14 - Gene Mutation, DNA Repair, and Transposition34
- Ch. 15 - Regulation of Gene Expression in Bacteria22
- Ch. 16 - Regulation of Gene Expression in Eukaryotes37
- Ch. 17 - Recombinant DNA Technology27
- Ch. 18 - Genomics, Bioinformatics, and Proteomics30
- Ch. 19 - The Genetics of Cancer21
- Ch. 20 - Quantitative Genetics and Multifactorial Traits37
- Ch. 21 - Population and Evolutionary Genetics45
Chapter 16, Problem 6
Present an overview of the manner in which chromatin can be remodeled. Describe the manner in which these remodeling processes influence transcription.
Verified step by step guidance1
Begin by defining chromatin remodeling as the dynamic modification of chromatin architecture to allow access of condensed genomic DNA to the regulatory transcription machinery proteins, thereby controlling gene expression.
Explain the two main mechanisms of chromatin remodeling: (1) covalent modifications of histone proteins (such as acetylation, methylation, phosphorylation) and (2) ATP-dependent chromatin remodeling complexes that reposition or evict nucleosomes.
Describe how histone acetylation, typically carried out by histone acetyltransferases (HATs), neutralizes positive charges on histones, decreasing their affinity for DNA and resulting in a more open chromatin structure that facilitates transcription.
Discuss how ATP-dependent remodeling complexes use energy from ATP hydrolysis to slide nucleosomes along DNA, eject nucleosomes, or restructure nucleosome composition, thereby exposing promoter and enhancer regions to transcription factors and RNA polymerase.
Conclude by linking these remodeling processes to transcriptional regulation: open chromatin states generally promote transcription by allowing transcription factor binding, while closed or condensed chromatin states repress transcription by restricting access to DNA.
Key Concepts
Here are the essential concepts you must grasp in order to answer the question correctly.
Chromatin Structure and Organization
Chromatin is composed of DNA wrapped around histone proteins forming nucleosomes, which further fold into higher-order structures. Its organization regulates DNA accessibility, influencing gene expression by controlling how tightly or loosely DNA is packed.
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Chromatin
Mechanisms of Chromatin Remodeling
Chromatin remodeling involves ATP-dependent complexes that reposition, eject, or restructure nucleosomes to alter DNA accessibility. These changes enable or restrict the binding of transcription factors and RNA polymerase to DNA, thereby regulating gene activity.
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Impact of Chromatin Remodeling on Transcription
By modifying chromatin structure, remodeling processes either facilitate or hinder transcription initiation and elongation. Open chromatin states promote transcription by allowing factor binding, while closed states repress gene expression by limiting access to DNA.
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Related Practice
Textbook Question
Provide a brief description of two different types of histone modification and how they impact transcription.
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Textbook Question
Distinguish between the cis-acting regulatory elements referred to as promoters and enhancers.
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Textbook Question
Describe the manner in which activators and repressors influence the rate of transcription initiation. How might chromatin structure be involved in such regulation?
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Textbook Question
Many promoter regions contain CAAT boxes containing consensus sequences CAAT or CCAAT approximately 70 to 80 bases upstream from the transcription start site. How might one determine the influence of CAAT boxes on the transcription rate of a given gene?
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