Chromatin assembly factor I and Hir proteins contribute to building functional kinetochores in S-cerevisiae

被引:120
作者
Sharp, JA
Franco, AA
Osley, MA
Kaufman, PD [1 ]
机构
[1] Univ Calif Berkeley, Lawrence Berkeley Lab, Berkeley, CA 94720 USA
[2] Univ Calif Berkeley, Dept Mol & Cell Biol, Berkeley, CA 94720 USA
[3] Univ New Mexico, Hlth Sci Ctr, Dept Mol Genet & Microbiol, Albuquerque, NM 87131 USA
关键词
centromere; kinetochore; historic; yeast; checkpoint; chromatin;
D O I
10.1101/gad.925302
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Budding yeast centromeres are comprised of similar to125-bp DNA sequences that direct formation of the kinetochore, a specialized chromatin structure that mediates spindle attachment to chromosomes. We report here a novel role for the historic deposition complex chromatin assembly factor I (CAF-I) in building centromeric chromatin. The contribution of CAF-I to kinetochore function overlaps that of the Hit proteins, which have also been implicated in nucleosome formation and heterochromatic gene silencing. cacDelta hirDelta double mutant cells lacking both CAF-I and Hir proteins are delayed in anaphase entry in a spindle assembly checkpoint-dependent manner. Further, cacDelta and hirDelta deletions together cause increased rates of chromosome missegregation, genetic synergies with mutations in kinetochore protein genes, and alterations in centromeric chromatin structure. Finally, CAF-I subunits and Hir1 are enriched at centromeres, indicating that these proteins make a direct contribution to centromeric chromatin structures.
引用
收藏
页码:85 / 100
页数:16
相关论文
共 99 条
[31]   EVIDENCE THAT SNF2/SWI2 AND SNF5 ACTIVATE TRANSCRIPTION IN YEAST BY ALTERING CHROMATIN STRUCTURE [J].
HIRSCHHORN, JN ;
BROWN, SA ;
CLARK, CD ;
WINSTON, F .
GENES & DEVELOPMENT, 1992, 6 (12A) :2288-2298
[32]   Exit from mitosis: Spindle pole power [J].
Hoyt, MA .
CELL, 2000, 102 (03) :267-270
[33]   Ctf19p:: A novel kinetochore protein in Saccharomyces cerevisiae and a potential link between the kinetochore and mitotic spindle [J].
Hyland, KM ;
Kingsbury, J ;
Koshland, D ;
Hieter, P .
JOURNAL OF CELL BIOLOGY, 1999, 145 (01) :15-28
[34]  
Hyman AA, 1995, ANNU REV CELL DEV BI, V11, P471, DOI 10.1146/annurev.cb.11.110195.002351
[35]  
Jin QW, 2000, J CELL SCI, V113, P1903
[36]   Yeast nuclei display prominent centromere clustering that is reduced in nondividing cells and in meiotic prophase [J].
Jin, QW ;
Trelles-Sticken, E ;
Scherthan, H ;
Loidl, J .
JOURNAL OF CELL BIOLOGY, 1998, 141 (01) :21-29
[37]  
Kamakaka RT, 1996, MOL CELL BIOL, V16, P810
[38]   The case for epigenetic effects on centromere identity and function [J].
Karpen, GH ;
Allshire, RC .
TRENDS IN GENETICS, 1997, 13 (12) :489-496
[39]   Hir proteins are required for position-dependent gene silencing in Saccharomyces cerevisiae in the absence of chromatin assembly factor I [J].
Kaufman, PD ;
Cohen, JL ;
Osley, MA .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (08) :4793-4806
[40]   Ultraviolet radiation sensitivity and reduction of telomeric silencing Saccharomyces cerevisiae cells lacking chromatin assembly factor-I [J].
Kaufman, PD ;
Kobayashi, R ;
Stillman, B .
GENES & DEVELOPMENT, 1997, 11 (03) :345-357