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Expression
Alberts, Chapters 8
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Eucaryotic gene expression can be controlled at
several different steps
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The Transcription Cycle
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A Cluster Of Baterical Genes Can Be
Transcribed From A Single Promoter
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Genes can be switched on and off with repressor proteins: lessons
from tryptophan operon
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Gene expression can also be controlled with
activator proteins
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An Activator and a Repressor Control lac Operon
Activator CAP binds to DNA activation sequence when it binds with cAMP
Repressor binds to the operator sequence.
Allolactose binds to the repressor protein and removes it from the DNA.
Addition of lactose increase the concentration of allolactose.
Addition of glucose decrease the concentration of cAMP.
1. RNA polymerases;
2. Transcription factors;
3. Eucaryotic gene regulatory proteins control
gene expression from a distance;
4. DNA package.
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Eucaryptic RNA
polymerase II
requires general
transcription
factors to initiate
transcription
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In eucaryotes, gene activation occurs at a distance
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Initiation of Eucaryptic Gene Transcription
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Regulatory proteins work together as a committee to
control the expression of a eucaryptic gene
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Even-skipped-eve in the big egg of
Drosophila
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Modular construction of the eve gene regulatory regions
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Four gene regulatory proteins distribute unevenly in
the early fly embryo
Activator Repressor
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Figure 8-14 Essential Cell Biology ( Garland Science 2010)
The regulatory module for eve stripe 2 contains
binding sites for four different gene regulatory proteins
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Figure 8-14 Essential Cell Biology ( Garland Science 2014)
A single transcription regulator can coordinated
the expression of many different genes
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Transcription factors consist of discrete, functional modules.
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A gene regulatory protein binds to the major
groove of a DNA helix
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Gene regulartory
proteins contain a
variety of DNA
binding motifs
Helix turn-helix
Zinc finger
Leucine zipper
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Transcription factor dimers that recognize novel targets
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Chapter 8 Study Guide. Control of Gene Expression
Overall Goal: Understand how gene expression is regulated, especially at the transcriptional level.
Specific Objectives:
4) Know how enhancers work to regulate transcription, and how combinations of different proteins can work
through them to regulate gene expression.
5) Understand that chromatin structure and histone modifications can strongly influence gene expression.
6) Combine the information in this chapter, especially Fig 8-3, with what you learned in Chapter 7, to
understand how RNA splicing (processing), RNA export, and translational control can be regulated to control
the expression of proteins in a cell.
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Chapter 9
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The tree of life has three major divisions
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Phylogenetic trees display the relationships among modern life forms
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Features of evolutionary
sequence conservation
in closely related species
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Figure 9-22 Essential Cell Biology ( Garland Science 2010)
The puffer fish, Fugu rubripes, has a remarkable compact genome
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Gene duplication can occur by crossover
between short repeated sequence on DNA
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Exon shuffling can generate proteins with
new combinations of protein domains
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The positions of mobil genetic elements in the human and
mouse genomes reflect the long evolutionary time
separating the two species
09_18_transposons.jpg
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Figure 9-20 Essential Cell Biology ( Garland Science 2010)
Chapter 9 Study Guide. How Genes and Genomes evolve
Overall Goals: Understand what the patterns of sequence conservation and sequence differences reveals about gene structure,
function, and evolution. Understand the fundamental means by which genomes change in structure over time.
Specific Objectives:
1) Know how to interpret the relationships in simple phylogenetic trees.
2) Be able to interpret the pattern of sequence conservation and divergence to extract information about gene structure and
regulatory information.
3) Recognize that much of the genome is repetitive and that much of it consists of transposable elements
4) Understand how mutations, duplications, and exon duplications and exon shuffling can influence genome evolution.
Problems:
9-3, 9-8, 9-9, 9-12, 9-14, 9-15, 9-17. Do all these problems. In addition to addressing molecular evolution, they are useful review
for much material in Chapters 5, 6, 7, and 8.
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