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Genetic evidence that Ras-like GTPases, Gtr1p, and Gtr2p, are involved in epigenetic control of gene expression in Saccharomyces cerevisiae
被引:11
|作者:
Sekiguchi, Takeshi
[1
,3
]
Hayashi, Naoyuki
[2
]
Wang, Yonggang
[1
]
Kobayashi, Hideki
[1
,3
]
机构:
[1] Kyushu Univ, Grad Sch Med Sci, Dept Mol Biol, Higashi Ku, Fukuoka 8128582, Japan
[2] Kanazawa Univ, Inst Canc Res, Dept Mol Pathol, Kanazawa, Ishikawa 9200934, Japan
[3] Japan Sci & Technol Agcy, CREST, Tokyo 1030027, Japan
基金:
日本科学技术振兴机构;
关键词:
Gtr1p;
Gtr2p;
Rvb2p;
Ino80p;
TOR;
D O I:
10.1016/j.bbrc.2008.01.133
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:
Gtr1p and Gtr2p of Saccharomyces cerevisiae are members of the Ras-like GTP binding family and interact genetically with Prp20p (yeast RCC1), which is a guanine nucleotide exchange factor for Gsp1p (yeast homolog of Ran, involved in nuclear export). Recently, Gtr1p and Gtr2p were suggested to be molecular switches in the rapamycin-sensitive TOR signaling pathway. Here, we show that Gtr1p and Gtr2p genetically interact with the chromatin remodeling factor Ino80p. Gtr2p interacted physically with both Rvb1p and Rvb2p. Consistent with these results, Gtr2p localized to chromatin and could activate transcription. Gtr1p and Gtr2p were found to be involved in chromatin silencing in the vicinity of telomeres. Gtr1p and Gtr2p were required to repress nitrogen catabolite-repressed genes, which are repressed by the TOR signaling pathway. We propose that Gtr1p and Gtr2p are involved in epigenetic control of gene expression in the TOR signaling pathway. (c) 2008 Elsevier Inc. All rights reserved.
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页码:748 / 754
页数:7
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