Affiliation:
1. Department of Biology, University of Rochester, Rochester, New York 14627
Abstract
ABSTRACT
Tetrahymena thermophila
macronuclear histone H1 is phosphorylated by a cdc2 kinase, and H1 phosphorylation regulates
CDC2
expression by a positive feedback mechanism. In starved wild-type cells, decreased expression of the
CDC2
gene is correlated with a global reduction in the phosphorylation of H1 and reduced phosphorylation of H1 in the region upstream of the
CDC2
gene. To determine whether the reduced H1 phosphorylation upstream of the
CDC2
gene is merely a reflection of global dephosphorylation or is due to specific targeting of dephosphorylation of H1 to the
CDC2
promoter during starvation, the
CDC2
promoter was mapped, and the distributions of phosphorylated and unphosphorylated H1 across the
CDC2
gene were determined using chromatin immunoprecipitation. Unphosphorylated H1 is specifically enriched in a region of the
CDC2
promoter when the gene's expression is reduced during starvation but not when
CDC2
is highly active in growing cells. The region of unphosphorylated H1 coincides with a region that is essential for
CDC2
expression. These studies are the first in vivo demonstration that the phosphorylation of H1 is being regulated at a fine level and that unphosphorylated H1 can be specifically targeted to a promoter, where it likely regulates transcription in a gene-specific manner.
Publisher
American Society for Microbiology
Subject
Cell Biology,Molecular Biology
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