Cell cycle-dependent regulation of RNA polymerase I transcription:: The nucleolar transcription factor UBF is inactive in mitosis and early G1

被引:146
作者
Klein, J [1 ]
Grummt, I [1 ]
机构
[1] German Canc Res Ctr, Div Mol Biol Cell 2, D-69120 Heidelberg, Germany
关键词
transcription initiation factor IB; SL1; repression; phosphorylation;
D O I
10.1073/pnas.96.11.6096
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Transcription of ribosomal RNA genes by RNA polymerase (pol) I oscillates during the cell cycle, being maximal in S and G(2) phase, repressed during mitosis, and gradually recovering during G(1) progression. We have shown that transcription initiation factor (TIF)-IB/SL1 is inactivated during mitosis by cdc2/cyclin B-directed phosphorylation of TAF(I)110, In this study, we have monitored reactivation of transcription after exit from mitosis. We demonstrate that the pol I factor UBF is also inactivated by phosphorylation but recovers with different kinetics than TIF-IB/SL1. Whereas TIF-IB/SL1 activity is rapidly regained on entry into G(1), UBF is reactivated later in G(1), concomitant with the onset of pol I transcription, Repression of pol I transcription in mitosis and early G(1) can be reproduced with either extracts from cells synchronized in M or G(1) phase or with purified TIF-IB/SL1 and UBF isolated in the presence of phosphatase inhibitors. The results suggest that two basal transcription factors, e.g., TIF-IB/SL1 and UBF, are inactivated at mitosis and reactivated by dephosphorylation at the exit from mitosis and during G(1) progression, respectively.
引用
收藏
页码:6096 / 6101
页数:6
相关论文
共 34 条
[1]   The molecular mechanism of mitotic inhibition of TFIIH is mediated by phosphorylation of CDK7 [J].
Akoulitchev, S ;
Reinberg, D .
GENES & DEVELOPMENT, 1998, 12 (22) :3541-3550
[2]   INHIBITORY EFFECT OF A MARINE-SPONGE TOXIN, OKADAIC ACID, ON PROTEIN PHOSPHATASES - SPECIFICITY AND KINETICS [J].
BIALOJAN, C ;
TAKAI, A .
BIOCHEMICAL JOURNAL, 1988, 256 (01) :283-290
[3]   DISTINCT TFIID COMPLEXES MEDIATE THE EFFECT OF DIFFERENT TRANSCRIPTIONAL ACTIVATORS [J].
BROU, C ;
CHAUDHARY, S ;
DAVIDSON, I ;
LUTZ, Y ;
WU, J ;
EGLY, JM ;
TORA, L ;
CHAMBON, P .
EMBO JOURNAL, 1993, 12 (02) :489-499
[4]   ACTIVITY OF RNA-POLYMERASE-I TRANSCRIPTION FACTOR UBF BLOCKED BY RB GENE-PRODUCT [J].
CAVANAUGH, AH ;
HEMPEL, WM ;
TAYLOR, LJ ;
ROGALSKY, V ;
TODOROV, G ;
ROTHBLUM, LI .
NATURE, 1995, 374 (6518) :177-180
[5]   PHOSPHORYLATION OF RNA-POLYMERASE BY THE MURINE HOMOLOG OF THE CELL-CYCLE CONTROL PROTEIN-CDC2 [J].
CISEK, LJ ;
CORDEN, JL .
NATURE, 1989, 339 (6227) :679-684
[6]   THE TATA-BINDING PROTEIN AND ASSOCIATED FACTORS ARE INTEGRAL COMPONENTS OF THE RNA POLYMERASE-I TRANSCRIPTION FACTOR, SL1 [J].
COMAI, L ;
TANESE, N ;
TJIAN, R .
CELL, 1992, 68 (05) :965-976
[7]   A TBP-CONTAINING MULTIPROTEIN COMPLEX (TIF-IB) MEDIATES TRANSCRIPTION SPECIFICITY OF MURINE RNA POLYMERASE-I [J].
EBERHARD, D ;
TORA, L ;
EGLY, JM ;
GRUMMT, I .
NUCLEIC ACIDS RESEARCH, 1993, 21 (18) :4180-4186
[8]   Mitotic repression of the transcriptional machinery [J].
Gottesfeld, JM ;
Forbes, DJ .
TRENDS IN BIOCHEMICAL SCIENCES, 1997, 22 (06) :197-202
[9]   MITOTIC REPRESSION OF RNA POLYMERASE-III TRANSCRIPTION IN-VITRO MEDIATED BY PHOSPHORYLATION OF A TFIIIB COMPONENT [J].
GOTTESFELD, JM ;
WOLF, VJ ;
DANG, T ;
FORBES, DJ ;
HARTL, P .
SCIENCE, 1994, 263 (5143) :81-84
[10]   RNA polymerase I associated factor 53 binds to the nucleolar transcription factor UBF and functions in specific rDNA transcription [J].
Hanada, K ;
Song, CZ ;
Yamamoto, K ;
Yano, K ;
Maeda, Y ;
Yamaguchi, K ;
Muramatsu, M .
EMBO JOURNAL, 1996, 15 (09) :2217-2226