Quantitative contributions of CtBP-dependent and -independent repression activities of Knirps

被引:23
作者
Struffi, P
Corado, M
Kulkarni, M
Arnosti, DN [1 ]
机构
[1] Michigan State Univ, Dept Biochem & Mol Biol, E Lansing, MI 48824 USA
[2] Michigan State Univ, Genet Program, E Lansing, MI 48824 USA
[3] NYU, Dept Biol, New York, NY 10031 USA
来源
DEVELOPMENT | 2004年 / 131卷 / 10期
关键词
CtBP; Knirps; even-skipped; enhancer; repression; transcription; Drosophila;
D O I
10.1242/dev.01075
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The Drosophila Knirps protein is a short-range transcriptional repressor that locally inhibits activators by recruiting the CtBP co-repressor. Knirps also possesses CtBP-independent repression activity. The functional importance of multiple repression activities is not well understood, but the finding that Knirps does not repress some cis-regulatory elements in the absence of CtBP suggested that the co-factor may supply a unique function essential to repress certain types of activators. We assayed CtBP-dependent and -independent repression domains of Knirps; in Drosophila embryos, and found that the CtBP-independent activity, when provided at higher than normal levels, can repress an eve regulatory element that normally requires CtBP. Dose response analysis revealed that the activity of Knirps containing both CtBP-dependent and -independent repression activities is higher than that of the CtBP-independent domain alone. The requirement for CtBP at certain enhancers appears to reflect the need for overall higher levels of repression, rather than a requirement for an activity unique to CtBP. Thus, CtBP contributes quantitatively, rather than qualitatively, to overall repression function. The finding that both repression activities are simultaneously deployed suggests that the multiple repression activities do not function as cryptic 'backup' systems, but that each contributes quantitatively to total repressor output.
引用
收藏
页码:2419 / 2429
页数:11
相关论文
共 55 条
[1]   The gap protein knirps mediates both quenching and direct repression in the Drosophila embryo [J].
Arnosti, DN ;
Gray, S ;
Barolo, S ;
Zhou, JM ;
Levine, M .
EMBO JOURNAL, 1996, 15 (14) :3659-3666
[2]   Groucho-dependent and -independent repression activities of runt domain proteins [J].
Aronson, BD ;
Fisher, AL ;
Blechman, K ;
Caudy, M ;
Gergen, JP .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (09) :5581-5587
[3]   Nicotinamide adenine dinucleotide stimulates oligomerization, interaction with adenovirus E1A and an intrinsic dehydrogenase activity of CtBP [J].
Balasubramanian, P ;
Zhao, LJ ;
Chinnadurai, G .
FEBS LETTERS, 2003, 537 (1-3) :157-160
[4]   Exploiting transcription factor binding site clustering to identify cis-regulatory modules involved in pattern formation in the Drosophila genome [J].
Berman, BP ;
Nibu, Y ;
Pfeiffer, BD ;
Tomancak, P ;
Celniker, SE ;
Levine, M ;
Rubin, GM ;
Eisen, MB .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2002, 99 (02) :757-762
[5]  
CARROLL SB, 1986, CELL, V45, P113, DOI 10.1016/0092-8674(86)90543-X
[6]   EUKARYOTIC START AND STOP TRANSLATION SITES [J].
CAVENER, DR ;
RAY, SC .
NUCLEIC ACIDS RESEARCH, 1991, 19 (12) :3185-3192
[7]   CtBP, an unconventional transcriptional corepressor in development and oncogenesis [J].
Chinnadurai, G .
MOLECULAR CELL, 2002, 9 (02) :213-224
[8]   A self-organizing system of repressor gradients establishes segmental complexity in Drosophila [J].
Clyde, DE ;
Corado, MSG ;
Wu, XL ;
Paré, A ;
Papatsenko, D ;
Small, S .
NATURE, 2003, 426 (6968) :849-853
[9]  
Fujioka M, 1999, DEVELOPMENT, V126, P2527
[10]  
Fujioka M, 2002, DEVELOPMENT, V129, P4411