Functional overlap of sequences that activate transcription and signal ubiquitin-mediated proteolysis

被引:226
作者
Salghetti, SE
Muratani, M
Wijnen, H
Futcher, B
Tansey, WP
机构
[1] Cold Spring Harbor Lab, Cold Spring Harbor, NY 11724 USA
[2] SUNY Stony Brook, Grad Program Genet, Stony Brook, NY 11792 USA
关键词
D O I
10.1073/pnas.050007597
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
Many transcription factors, particularly those involved in the control of cell growth, are unstable proteins destroyed by ubiquitin-mediated proteolysis. In a previous study of sequences targeting the transcription factor Myc for destruction, we observed that the region in Myc signaling ubiquitin-mediated proteolysis overlaps closely with the region in Myc that activates transcription. Here, we present evidence that the overlap of these two activities is not unique to Myc, but reflects a more general phenomenon. We show that a similar overlap of activation domains and destruction elements occurs in other unstable transcription factors and report a close correlation between the ability of an acidic activation domain to activate transcription and to signal proteolysis. We also show that destruction elements from yeast cyclins, when tethered to a DNA-binding domain, activate transcription. The intimate overlap of activation domains and destruction elements reveals an unexpected convergence of two very different processes and suggests that transcription factors may he destroyed because of their ability to activate transcription.
引用
收藏
页码:3118 / 3123
页数:6
相关论文
共 49 条
[1]   CONTROL OF C-JUN ACTIVITY BY INTERACTION OF A CELL-SPECIFIC INHIBITOR WITH REGULATORY DOMAIN-DELTA - DIFFERENCES BETWEEN V-JUN AND C-JUN [J].
BAICHWAL, VR ;
TJIAN, R .
CELL, 1990, 63 (04) :815-825
[2]   Identification of protein instability determinants in the carboxy-terminal region of c-myb removed as a result of retroviral integration in murine monocytic leukemias [J].
Bies, J ;
Nazarov, V ;
Wolff, L .
JOURNAL OF VIROLOGY, 1999, 73 (03) :2038-2044
[3]   AN INHIBITOR DOMAIN IN C-FOS REGULATES ACTIVATION DOMAINS CONTAINING THE HOB1 MOTIF [J].
BROWN, HJ ;
SUTHERLAND, JA ;
COOK, A ;
BANNISTER, AJ ;
KOUZARIDES, T .
EMBO JOURNAL, 1995, 14 (01) :124-131
[4]   Regulation of E2F through ubiquitin-proteasome-dependent degradation: Stabilization by the pRB tumor suppressor protein [J].
Campanero, MR ;
Flemington, EK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (06) :2221-2226
[5]   Degradation of proto-oncoprotein c-Rel by the ubiquitin-proteasome pathway [J].
Chen, E ;
Hrdlickova, R ;
Nehyba, J ;
Longo, DL ;
Bose, HR ;
Li, CCH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (52) :35201-35207
[6]  
CHEN RH, 1995, ONCOGENE, V11, P1771
[7]   ACCUMULATION OF P53 IN A MUTANT-CELL LINE DEFECTIVE IN THE UBIQUITIN PATHWAY [J].
CHOWDARY, DR ;
DERMODY, JJ ;
JHA, KK ;
OZER, HL .
MOLECULAR AND CELLULAR BIOLOGY, 1994, 14 (03) :1997-2003
[8]   ANALYSIS OF SP1 INVIVO REVEALS MULTIPLE TRANSCRIPTIONAL DOMAINS, INCLUDING A NOVEL GLUTAMINE-RICH ACTIVATION MOTIF [J].
COUREY, AJ ;
TJIAN, R .
CELL, 1988, 55 (05) :887-898
[9]   IκB is a substrate for a selective pathway of lysosomal proteolysis [J].
Cuervo, AM ;
Hu, W ;
Lim, B ;
Dice, JF .
MOLECULAR BIOLOGY OF THE CELL, 1998, 9 (08) :1995-2010
[10]   LEVEL OF UBIQUITINATED HISTONE H2B IN CHROMATIN IS COUPLED TO ONGOING TRANSCRIPTION [J].
DAVIE, JR ;
MURPHY, LC .
BIOCHEMISTRY, 1990, 29 (20) :4752-4757