The Caenorhabditis elegans schnurri homolog sma-9 mediates stage- and cell type-specific responses to DBL-1 BMP-related signaling

被引:55
作者
Liang, J
Lints, R
Foehr, ML
Tokarz, R
Yu, L
Emmons, SW
Liu, J
Savage-Dunn, C [1 ]
机构
[1] CUNY Queens Coll, Dept Biol, Flushing, NY 11367 USA
[2] CUNY Queens Coll, Grad Sch & Univ Ctyr, PhD Program Biochem, Flushing, NY 11367 USA
[3] Yeshiva Univ Albert Einstein Coll Med, Dept Mol Genet, Bronx, NY 10461 USA
[4] Yeshiva Univ Albert Einstein Coll Med, Dept Neurosci, Bronx, NY 10461 USA
[5] Cornell Univ, Dept Mol Biol & Genet, Ithaca, NY 14853 USA
来源
DEVELOPMENT | 2003年 / 130卷 / 26期
关键词
BMP; schnurri; transcription factor; body size; pattern formation; alternative splicing;
D O I
10.1242/dev.00863
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
In Caenorhabditis elegans, the DBL-1 pathway, a BMP/TGFbeta-related signaling cascade, regulates body size and male tail development. We have cloned a new gene, sma-9, that encodes the C elegans homolog of Schnurri, a large zinc finger transcription factor that regulates dpp target genes in Drosophila. Genetic interactions, the sma-9 loss-of-function phenotype, and the expression pattern suggest that sma-9 acts as a downstream component and is required in the DBL-1 signaling pathway, and thus provide the first evidence of a conserved role for Schnurri proteins in BMP signaling. Analysis of sma-9 mutant phenotypes demonstrates that SMA-9 activity is temporally and spatially restricted relative to known DBL-1 pathway components. In contrast with Drosophila schnurri, the presence of multiple alternatively spliced sma-9 transcripts suggests protein isoforms with potentially different cell sublocalization and molecular functions. We propose that SMA-9 isoforms function as transcriptional cofactors that confer specific responses to DBL-1 pathway activation.
引用
收藏
页码:6453 / 6464
页数:12
相关论文
共 56 条
[1]   THE DROSOPHILA SCHNURRI GENE ACTS IN THE DPP/TGF-BETA SIGNALING PATHWAY AND ENCODES A TRANSCRIPTION FACTOR HOMOLOGOUS TO THE HUMAN MBP FAMILY [J].
ARORA, K ;
DAI, H ;
KAZUKO, SG ;
JAMAL, J ;
OCONNOR, MB ;
LETSOU, A ;
WARRIOR, R .
CELL, 1995, 81 (05) :781-790
[2]  
Barr MM, 1999, NATURE, V401, P386, DOI 10.1038/43913
[3]   A global analysis of Caenorhabditis elegans operons [J].
Blumenthal, T ;
Evans, D ;
Link, CD ;
Guffanti, A ;
Lawson, D ;
Thierry-Mieg, J ;
Thierry-Mieg, D ;
Chiu, WL ;
Duke, K ;
Kiraly, M ;
Kim, SK .
NATURE, 2002, 417 (6891) :851-854
[4]  
BRENNER S, 1974, GENETICS, V77, P71
[5]   Transducing the Dpp morphogen gradient in the wing of Drosophila:: Regulation of Dpp targets by brinker [J].
Campbell, G ;
Tomlinson, A .
CELL, 1999, 96 (04) :553-562
[6]   A transcriptional partner for MAD proteins in TGF-beta signalling [J].
Chen, X ;
Rubock, MJ ;
Whitman, M .
NATURE, 1996, 383 (6602) :691-696
[7]  
Collet J, 1998, GENETICS, V148, P187
[8]   The zinc finger protein schnurri nets as a smad partner in mediating the transcriptional response to decapentaplegic [J].
Dai, H ;
Hogan, C ;
Gopalakrishnan, B ;
Torres-Vazquez, J ;
Nguyen, M ;
Park, SB ;
Raftery, LA ;
Warrior, R ;
Arora, K .
DEVELOPMENTAL BIOLOGY, 2000, 227 (02) :373-387
[9]   THE DAF-4 GENE ENCODES A BONE MORPHOGENETIC PROTEIN-RECEPTOR CONTROLLING C-ELEGANS DAUER LARVA DEVELOPMENT [J].
ESTEVEZ, M ;
ATTISANO, L ;
WRANA, JL ;
ALBERT, PS ;
MASSAGUE, J ;
RIDDLE, DL .
NATURE, 1993, 365 (6447) :644-649
[10]   A DNA-BINDING PROTEIN CONTAINING 2 WIDELY SEPARATED ZINC FINGER MOTIFS THAT RECOGNIZE THE SAME DNA-SEQUENCE [J].
FAN, CM ;
MANIATIS, T .
GENES & DEVELOPMENT, 1990, 4 (01) :29-42