ESSENTIALS OF GENETICS ALC & MOD MSTG/ET VP
ESSENTIALS OF GENETICS ALC & MOD MSTG/ET VP
1st Edition
ISBN: 9780134452890
Author: KLUG
Publisher: Pearson Education
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Chapter 11, Problem 18PDQ
Summary Introduction

To review:

The effect of chemical modifications of histone proteins on nucleosome–DNA (deoxyribonucleic acid) interactions and gene activity.

Introduction:

Nucleosomes are the basic unit of packaging of the DNA molecule in eukaryotes. The nucleosome is folded in a successive ordered manner to form a chromosome. Nucleosome core particles consist of DNA molecules wrapped around the histone proteins. Histone protein is present as an octamer having two copies of each H2A, H2B, H3, and H4 in the core and a linker histone H1 that is associated with the linker DNA present between the two nucleosomes.

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What chemical and structural properties of histones enable them to successfully package eukaryotic DNA? What is chromatin remodeling, and how is it controlled within eukaryotic cells?
Glenn Croston and his colleagues studied the relation between chromatin structure and transcription activity. In one set of experiments, they measured the level of in vitro transcription of a Drosophila gene by RNA polymerase II in the presence of DNA and various combinations of histone proteins (G. E. Croston et al. 1991. Science 251:643–649). First, they measured the level of transcription of naked DNA, with no associated histone proteins. Then they measured the level of transcription after nucleosome octamers (without H1) were added to the DNA. The addition of the octamers caused the level of transcription to drop by 50%. When both nucleosome octamers and H1 proteins were added to the DNA, transcription was greatly repressed, dropping to less than 1% of that obtained with naked DNA, as shown in the table below. GAL4-VP16 is a protein that binds to the DNA of certain eukaryotic genes. When GAL4-VP16 is added to DNA, the level of transcription by RNA polymerase II is greatly elevated.…
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