Human slug is a repressor that localizes to sites of active transcription

被引:110
作者
Hemavathy, K
Guru, SC
Harris, J
Chen, JD
Ip, YT
机构
[1] Univ Massachusetts, Sch Med, Dept Cell Biol, Program Mol Med, Worcester, MA 01605 USA
[2] Univ Massachusetts, Sch Med, Dept Biochem & Mol Biol, Worcester, MA 01605 USA
[3] Univ Massachusetts, Sch Med, Dept Mol Pharmacol & Toxicol, Worcester, MA 01605 USA
[4] Natl Human Genome Res Inst, Genet & Mol Biol Branch, NIH, Bethesda, MD 20892 USA
关键词
D O I
10.1128/MCB.20.14.5087-5095.2000
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
Snail/Slug family proteins have been identified in diverse species of both vertebrates and invertebrates. The proteins contain four to six zinc fingers and function as DNA-binding transcriptional regulators. Various members of the family have been demonstrated to regulate cell movement, neural cell fate, left-right asymmetry, cell cycle, and apoptosis. However, the molecular mechanisms of how these regulators function and the target genes involved are largely unknown. In this report, we demonstrate that human Slug (hSlug) is a repressor and modulates both activator-dependent and basal transcription. The repression depends on the C-terminal DNA-binding zinc fingers and on a separable repression domain located in the N terminus. This domain may recruit histone deacetylases to modify the chromatin and effect repression. Protein localization study demonstrates that hSlug is present in discrete foci in the nucleus. This subnuclear pattern does not colocalize with the PML foci or the coiled bodies. Instead, the hSlug foci overlap extensively with areas of the SC-35 staining, some of which have been suggested to be sites of active splicing or transcription. These results lead us to postulate that hSlug localizes to target promoters, where activation occurs, to repress basal and activator-mediated transcription.
引用
收藏
页码:5087 / 5095
页数:9
相关论文
共 66 条
[1]  
ALBERGA A, 1991, DEVELOPMENT, V111, P983
[2]   The mesoderm determinant Snail collaborates with related zinc-finger proteins to control Drosophila neurogenesis [J].
Ashraf, SI ;
Hu, XD ;
Roote, J ;
Ip, YT .
EMBO JOURNAL, 1999, 18 (22) :6426-6438
[3]   Transcriptional control: Repression by local chromatin modification [J].
Ashraf, SI ;
Ip, YT .
CURRENT BIOLOGY, 1998, 8 (19) :R683-R686
[4]   Histone deacetylases: transcriptional repression with SINers and NuRDs [J].
Ayer, DE .
TRENDS IN CELL BIOLOGY, 1999, 9 (05) :193-198
[5]  
Bohmann K, 1995, J CELL SCI, P107
[6]   THE DROSOPHILA DEVELOPMENTAL GENE SNAIL ENCODES A PROTEIN WITH NUCLEIC-ACID BINDING FINGERS [J].
BOULAY, JL ;
DENNEFELD, C ;
ALBERGA, A .
NATURE, 1987, 330 (6146) :395-398
[7]   Inhibition of neural crest migration in Xenopus using antisense slug RNA [J].
Carl, TF ;
Dufton, C ;
Hanken, J ;
Klymkowsky, MW .
DEVELOPMENTAL BIOLOGY, 1999, 213 (01) :101-115
[8]   Identification of novel genes in Drosophila reveals the complex regulation of early gene activity in the mesoderm [J].
Casal, J ;
Leptin, M .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (19) :10327-10332
[9]   Coactivation and corepression in transcriptional regulation by steroid/nuclear hormone receptors [J].
Chen, JD ;
Li, H .
CRITICAL REVIEWS IN EUKARYOTIC GENE EXPRESSION, 1998, 8 (02) :169-190
[10]   Nuclear compartments and gene regulation [J].
Cockell, M ;
Gasser, SM .
CURRENT OPINION IN GENETICS & DEVELOPMENT, 1999, 9 (02) :199-205