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Chapter 17 Lecture
Concepts of Genetics Tenth Edition
Regulation of Gene Expression in Eukaryotes
Chapter Contents
17.1 Eukaryotic Gene Regulation Can Occur at Any of the Steps Leading from DNA to Protein Product
17.2 Programmed DNA Rearrangements Regulate Expression of a Small Number of Genes
17.3 Eukaryotic Gene Expression Is Influenced by Chromatin Modifications
17.4 Eukaryotic Transcription Initiation Is Regulated at Specific Cis-Acting Sites
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Chapter Contents
17.5 Eukaryotic Transcription Initiation Is Regulated by Transcription Factors That Bind to Cis-Acting Sites
17.6 Activators and Repressors Interact with General Transcription Factors at the Promoter
17.7 Gene Regulation in a Model Organism: Transcription of the GAL genes of Yeast
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Chapter Contents
17.8 Posttranscriptional Gene Regulation Occurs at All the Steps from RNA Processing to Protein Modification
17.9 RNA Silencing Controls Gene Expression in Several Ways
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17.1 Eukaryotic Gene Regulation Can Occur at Any of the Steps Leading from
DNA to Protein Product
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Section 17.1
• Gene regulation in eukaryotes is more complex than it is in prokaryotes because – of the larger amount of DNA that is associated with histones and
other proteins – most genes of mRNAs must be spliced, capped, and
polyadenylated prior to transport from nucleus – chromosomes with many genes are enclosed in a double
membrane nucleus – of movement of RNAs into cytoplasm after transcription – of RNA stability – of modulation of mRNA translation as well as protein processing,
modification, and degradation
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17.2 Programmed DNA Rearrangements Regulate Expression of a Small Number
of Genes
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Section 17.2
• Genomic DNA in most organisms is stable; however, some gene regulation by DNA rearrangement exists – DNA (gene) amplification – DNA rearrangements during developmental regulation
• Creation of new gene from gene fragments • Switch in expression of genes due to recombination • Loss of DNA sequences in somatic cells
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Section 17.2
• Antigen recognition allows the immune system to bind to foreign substances (antigens)
• Humoral immunity involves production of immunoglobins (antibodies) that directly bind to antigens – Synthesized by B cells that are made up of four variable regions
allowing recognition of a specific antigen – Each B cell synthesizes only one type of immunoglobulin
• DNA rearrangements can contribute to antibody diversity
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Section 17.2
• The human k light-chain gene is assembled during B-cell development from multiple regions along chromosome 2 – DNA regions organized into L (leader) and V (variable)
regions – Antibody diversity occurs in part from the random
recombination of one of 35–50 different functional LV regions with any of five different J regions
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Section 17.2
• Two other mechanisms further increase antibody diversity – Imprecise recombination between any particular pair
of LV and J regions shows considerable variation – High hypermutation (random somatic mutation)
introduces more variation into the LVJ region’s sequence
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17.3 Eukaryotic Gene Expression Is Influenced by Chromatin Modifications
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Section 17.3
• Chromosomes occupy a discrete territory in the nucleus and stay separate from other chromosomes – Transcription and translation spatially distinct
• Eukaryotic DNA combined with histone and non-histone proteins to form chromatin – Chromatin structure inhibits transcription, replication,
and DNA repair
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Section 17.3
• During interphase, each chromosome occupies a discrete area called chromosome territory
• Channels between chromosomes are called interchromosomal domains
• Chromosome structure is continuously rearranged so that transcriptionally active genes are cycled to the edges of chromosome territories
• Transcription factories are nuclear sites that contain most of the active RNA polymerase and transcription regulatory molecules
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Section 17.3
• Chromatin remodeling is an important step in gene regulation and involves changes to either the nucleosome or DNA
• Most histones contain normal histones H2A and H3 – Variant histones (H2A.Z and H3.3) can facilitate gene
transcription
• Histone acetylation of the nucleosome is catalyzed by histone acetyltransferase enzymes (HATs) and is associated with increased transcription
• Histones can also be modified by phosphorylation and methylation
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Section 17.3
• Chromatin remodeling involves repositioning or removal of nucleosomes on DNA
• Repositioned nucleosomes make regions of the chromosome accessible to transcription regulatory proteins – Transcription activators – RNA polymerase II
• The SWI/SNF is one of the best-studied remodeling complexes
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Section 17.3
• DNA methylation is associated with decreased gene expression
• Methylation occurs most often on the cytosine of CG doubled in DNA
• Methylation can repress transcription by binding to transcription factors of DNA
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17.4 Eukaryotic Transcription Initiation Is Regulated at Specific Cis-Acting Sites
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Section 17.4
• Transcription regulation requires binding of many regulatory factors to specific DNA sequences (cis-acting sequences) – Cis-acting sequence is located on the same
chromosome as the gene that it regulates – Promoters, Enhancers, Silencers
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Section 17.4
• Promoters are nucleotide sequences that serve as recognition sites for the transcription machinery – Critical for initiation of transcription – Located adjacent to genes regulated
• Great diversity exits in promoters in terms of
structure and function – Focused promoters: Specific transcription start site
– Dispersed promoters: Several start sites
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Section 17.4
• Promoters are made up of one or more core elements that bind to specific initiation proteins – Initiator (Inr), TATA box, TFIIB recognition element
(BRE), downstream promoter element (DPE), and motif ten element (MTE)
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• Many promoters contain proximal promoter elements located upstream of the TATA and BRE motifs, enhancing levels of basal transcription – CAAT and GC boxes
Section 17.4
• Enhancers (cis-acting) are modular and contain several short DNA sequences increasing transcription rates – Located on either side of gene, some distance from gene, or
even within the gene
• Silencers are cis-acting elements that repress the level of transcription initiation
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