Net1 stimulates RNA polymerase I transcription and regulates nucleolar structure independently of controlling mitotic exit

被引:104
作者
Shou, WY
Sakamoto, KM
Keener, J
Morimoto, KW
Traverso, EE
Azzam, R
Hoppe, GJ
Feldman, RMR
DeModena, J
Moazed, D
Charbonneau, H
Nomura, M
Deshaies, RJ [1 ]
机构
[1] CALTECH, Div Biol, Pasadena, CA 91125 USA
[2] CALTECH, Howard Hughes Med Inst, Pasadena, CA 91125 USA
[3] Univ Calif Irvine, Dept Biol Chem, Irvine, CA 92697 USA
[4] Harvard Univ, Sch Med, Dept Cell Biol, Boston, MA 02115 USA
[5] Purdue Univ, Dept Biochem, W Lafayette, IN 47907 USA
[6] Univ Calif Los Angeles, Sch Med, Dept Pediat & Pathol, Div Hematol Oncol, Los Angeles, CA 90095 USA
[7] Jonsson Comprehens Canc Ctr, Los Angeles, CA 90095 USA
[8] Free Univ Berlin, FB Biol Chem Pharm, D-14195 Berlin, Germany
[9] Pomona Coll, Dept Biol, Claremont, CA 91711 USA
关键词
D O I
10.1016/S1097-2765(01)00291-X
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 budding yeast RENT complex, consisting of at least three proteins (Net1, Cdc14, Sir2), is anchored to the nucleolus by Net1. RENT controls mitotic exit, nucleolar silencing, and nucleolar localization of Nop1. Here, we report two new functions of Net1. First, Net1 directly binds Pot I and stimulates rRNA synthesis both in vitro and in vivo. Second, Net1 modulates nucleolar structure by regulating rDNA morphology and proper localization of multiple nucleolar antigens, including Pol l. Importantly, we show that the nucleolar and previously described cell cycle functions of the RENT complex can be uncoupled by a dominant mutant allele of CDC14. The independent functions of Net1 link a key event in the cell cycle to nucleolar processes that are fundamental to cell growth.
引用
收藏
页码:45 / 55
页数:11
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