Isw1 functions in parallel with the NuA4 and Swr1 complexes in stress-induced gene repression

被引:54
作者
Lindstrom, Kimberly C.
Vary, Jay C., Jr.
Parthun, Mark R.
Delrow, Jeffrey
Tsukiyama, Toshio [1 ]
机构
[1] Fred Hutchinson Canc Res Ctr, Div Basic Sci, Seattle, WA 98109 USA
[2] Univ Washington, Fred Hutchinson Canc Res Ctr, Mol & Cellular Biol Program, Seattle, WA 98195 USA
[3] Ohio State Univ, Dept Mol & Cellular Biochem, Columbus, OH 43210 USA
[4] Fred Hutchinson Canc Res Ctr, Genom Resource, Seattle, WA 98109 USA
关键词
D O I
10.1128/MCB.00642-06
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The packaging of DNA into chromatin allows eukaryotic cells to organize and compact their genomes but also creates an environment that is generally repressive to nuclear processes that depend upon DNA accessibility. There are several classes of enzymes that modulate the primary structure of chromatin to regulate various DNA-dependent processes. The biochemical activities of the yeast Isw1 ATP-dependent chromatin-remodeling enzyme have been well characterized in vitro, but little is known about how these activities are utilized in vivo. In this work, we sought to discern genetic backgrounds that require Isw1 activity for normal growth. We identified a three-way genetic interaction among Isw1, the NuA4 histone acetyltransferase complex, and the Swr1 histone replacement complex. Transcription microarray analysis revealed parallel functions for these three chromatin-modifying factors in the regulation of TATA-containing genes, including the repression of a large number of stress-induced genes under normal growth conditions. In contrast to a recruitment-based model, we find that the NuA4 and Swr1 complexes act throughout the genome while only a specific subset of the genome shows alterations in transcription.
引用
收藏
页码:6117 / 6129
页数:13
相关论文
共 66 条
[31]   Functional consequences of histone modifications [J].
Iizuka, M ;
Smith, MM .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 2003, 13 (02) :154-160
[32]   Translating the histone code [J].
Jenuwein, T ;
Allis, CD .
SCIENCE, 2001, 293 (5532) :1074-1080
[33]   Histone variants: deviants? [J].
Kamakaka, RT ;
Biggins, S .
GENES & DEVELOPMENT, 2005, 19 (03) :295-310
[34]   Type B histone acetyltransferase Hat1p participates in telomeric silencing [J].
Kelly, TJ ;
Qin, S ;
Gottschling, DE ;
Parthun, MR .
MOLECULAR AND CELLULAR BIOLOGY, 2000, 20 (19) :7051-7058
[35]   The Saccharomyces cerevisiae histone H2A variant Htz1 is acetylated by NuA4 [J].
Keogh, MC ;
Mennella, TA ;
Sawa, C ;
Berthelet, S ;
Krogan, NJ ;
Wolek, A ;
Podolny, V ;
Carpenter, LR ;
Greenblatt, JF ;
Baetz, K ;
Buratowski, S .
GENES & DEVELOPMENT, 2006, 20 (06) :660-665
[36]   A protein complex containing the conserved Swi2/Snf2-related ATPase Swr1p deposits histone variant H2A.Z into euchromatin [J].
Kobor, MS ;
Venkatasubrahmanyam, S ;
Meneghini, MD ;
Gin, JW ;
Jennings, JL ;
Link, AJ ;
Madhani, HD ;
Rine, J .
PLOS BIOLOGY, 2004, 2 (05) :587-599
[37]   Regulation of chromosome stability by the histone H2A variant Htz1, the Swr1 chromatin remodeling complex, and the histone acetyltransferase NuA4 [J].
Krogan, NJ ;
Baetz, K ;
Keogh, MC ;
Datta, N ;
Sawa, C ;
Kwok, TCY ;
Thompson, NJ ;
Davey, MG ;
Pootoolal, J ;
Hughes, TR ;
Emili, A ;
Buratowski, S ;
Hieter, P ;
Greenblatt, JF .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2004, 101 (37) :13513-13518
[38]   A Snf2 family ATPase complex required for recruitment of the histone H2A variant Htz1 [J].
Krogan, NJ ;
Keogh, MC ;
Datta, N ;
Sawa, C ;
Ryan, OW ;
Ding, HM ;
Haw, RA ;
Pootoolal, J ;
Tong, A ;
Canadien, V ;
Richards, DP ;
Wu, XR ;
Emili, A ;
Hughes, TR ;
Buratowski, S ;
Greenblatt, JF .
MOLECULAR CELL, 2003, 12 (06) :1565-1576
[39]   Histone acetylation and deacetylation in yeast [J].
Kurdistani, SK ;
Grunstein, M .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2003, 4 (04) :276-284
[40]   Yaf9, a novel NuA4 histone acetyltransferase subunit, is required for the cellular response to spindle stress in yeast [J].
Le Masson, I ;
Yu, DY ;
Jensen, K ;
Chevalier, A ;
Courbeyrette, R ;
Boulard, Y ;
Smith, MM ;
Mann, C .
MOLECULAR AND CELLULAR BIOLOGY, 2003, 23 (17) :6086-6102