Mechanism of repression of RNA polymerase I transcription by the retinoblastoma protein

被引:139
作者
Voit, R [1 ]
Schafer, K [1 ]
Grummt, I [1 ]
机构
[1] GERMAN CANC RES CTR,DIV MOL BIOL CELL 2,D-69120 HEIDELBERG,GERMANY
关键词
D O I
10.1128/MCB.17.8.4230
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 retinoblastoma susceptibility gene product pRb restricts cellular proliferation by affecting gene expression by all three classes of nuclear RNA polymerases. To elucidate the molecular mechanisms underlying pRb-mediated repression of ribosomal DNA (rDNA) transcription hg RNA polymerase I, we have analyzed the effect of pRb in a reconstituted transcription system. We demonstrate that pRb, but not the related protein p107, acts as a transcriptional repressor by interfering with the assembly of transcription initiation complexes, The HMG box-containing transcription factor UBF is the main target for pRb-induced transcriptional repression, UBF and DRb form in vitro complexes involving the C-terminal part of pRb and HMG boxes 1 and 2 of UBF, We show that the interactions between UBF and TIF-IB and between UBF and RNA polymerase I, respectively, are not perturbed by pRb, However, the DNA binding activity of UBF to both synthetic cruciform DNA and the rDNA promoter is severely impaired in the presence of pRb, These studies reveal another mechanism by which pRb suppresses cell proliferation, namely, by direct inhibition of cellular rRNA synthesis.
引用
收藏
页码:4230 / 4237
页数:8
相关论文
共 50 条
[11]   E2F-4, A NEW MEMBER OF THE E2F TRANSCRIPTION FACTOR FAMILY, INTERACTS WITH P107 [J].
GINSBERG, D ;
VAIRO, G ;
CHITTENDEN, T ;
XIAO, ZX ;
XU, GF ;
WYDNER, KL ;
DECAPRIO, JA ;
LAWRENCE, JB ;
LIVINGSTON, DM .
GENES & DEVELOPMENT, 1994, 8 (22) :2665-2679
[12]   THE RETINOBLASTOMA GENE-PRODUCT REGULATES PROGRESSION THROUGH THE G1 PHASE OF THE CELL-CYCLE [J].
GOODRICH, DW ;
WANG, NP ;
QIAN, YW ;
LEE, EYHP ;
LEE, WH .
CELL, 1991, 67 (02) :293-302
[13]  
HEIBERT SW, 1993, MOL CELL BIOL, V13, P3384
[14]   Cloning of murine RNA polymerase I-specific TAF factors: Conserved interactions between the subunits of the species-specific transcription initiation factor TIF-IB/SL1 [J].
Heix, J ;
Zomerdijk, JCBM ;
Ravanpay, A ;
Tjian, R ;
Grummt, I .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (05) :1733-1738
[15]  
Hempel WM, 1996, MOL CELL BIOL, V16, P557
[16]   TUMOR-SUPPRESSOR GENES [J].
HINDS, PW ;
WEINBERG, RA .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1994, 4 (01) :135-141
[17]   REGULATION OF RETINOBLASTOMA PROTEIN FUNCTIONS BY ECTOPIC EXPRESSION OF HUMAN CYCLINS [J].
HINDS, PW ;
MITTNACHT, S ;
DULIC, V ;
ARNOLD, A ;
REED, SI ;
WEINBERG, RA .
CELL, 1992, 70 (06) :993-1006
[18]   RETINOBLASTOMA PROTEIN AND THE CELL-CYCLE [J].
HOLLINGSWORTH, RE ;
HENSEY, CE ;
LEE, WH .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1993, 3 (01) :55-62
[19]   THE REGIONS OF THE RETINOBLASTOMA PROTEIN NEEDED FOR BINDING TO ADENOVIRUS-E1A OR ADENOVIRUS-SV40 LARGE T-ANTIGEN ARE COMMON SITES FOR MUTATIONS [J].
HU, QJ ;
DYSON, N ;
HARLOW, E .
EMBO JOURNAL, 1990, 9 (04) :1147-1155
[20]   CYCLINS AND CANCER .2. CYCLIN-D AND CDK INHIBITORS COME OF AGE [J].
HUNTER, T ;
PINES, J .
CELL, 1994, 79 (04) :573-582