Previous Article | Next Article ![]()
Molecular and Cellular Biology, May 1999, p. 3624-3634, Vol. 19, No. 5
Department of Biology, Syracuse University,
Syracuse, New York 13244,1 and
Department of Biology, University of Rochester, Rochester,
New York 146272
Received 20 August 1998/Returned for modification 6 October
1998/Accepted 8 February 1999
Heterochromatin represents a specialized chromatin environment
vital to both the repression and expression of certain eukaryotic genes. One of the best-studied heterochromatin-associated proteins is
Drosophila HP1. In this report, we have disrupted all
somatic copies of the Tetrahymena HHP1 gene, which encodes
an HP1-like protein, Hhp1p, in macronuclei (H. Huang, E. A. Wiley,
R. C. Lending, and C. D. Allis, Proc. Natl. Acad. Sci. USA
95:13624-13629, 1998). Unlike the Drosophila HP1 gene,
HHP1 is not essential in Tetrahymena spp., and
during vegetative growth no clear phenotype is observed in cells
lacking Hhp1p (
0270-7306/99/$04.00+0
Copyright © 1999, American Society for Microbiology. All rights reserved.
A Nonessential HP1-Like Protein Affects
Starvation-Induced Assembly of Condensed Chromatin and Gene
Expression in Macronuclei of Tetrahymena
thermophila

and
HHP1). However, during a shift to
nongrowth conditions, the survival rate of
HHP1 cells is
reduced compared to that of wild-type cells. Upon starvation, Hhp1p
becomes hyperphosphorylated concomitant with a reduction in
macronuclear volume and an increase in the size of electron-dense
chromatin bodies; neither of these morphological changes occurs in the
absence of Hhp1p. Activation of two starvation-induced genes
(ngoA and CyP) is significantly reduced in
HHP1 cells while, in contrast, the expression of several growth-related or constitutively expressed genes is comparable to that
in wild-type cells. These results suggest that Hhp1p functions in the
establishment and/or maintenance of a specialized condensed chromatin
environment that facilitates the expression of certain genes linked to
a starvation-induced response.
*
Corresponding author. Present address: Department of
Biochemistry and Molecular Genetics, 6222 Jordan Hall, University of Virginia H.S.C., 1300 Jefferson Park Ave., Charlottesville, VA 22908. Phone: (804) 243-6048. Fax: (804) 924-5069. E-mail:
allis{at}virginia.edu.
Present address: Fred Hutchinson Cancer Research Center, Seattle,
WA 98109.
This article has been cited by other articles:
Copyright © 2010 by the American Society for Microbiology. For an alternate route to Journals.ASM.org, visit: http://intl-journals.asm.org | More Info»