The FoxF/FoxC factor LET-381 directly regulates both cell fate specification and cell differentiation in C. elegans mesoderm development

被引:21
作者
Amin, Nirav M. [1 ]
Shi, Herong [1 ]
Liu, Jun [1 ]
机构
[1] Cornell Univ, Dept Mol Biol & Genet, Ithaca, NY 14853 USA
来源
DEVELOPMENT | 2010年 / 137卷 / 09期
关键词
FoxF; FoxC; let-381; Forkhead domain; ceh-34; SIX2; homeodomain; eya-1; Eyes absent; Mesoderm; Cell fate specification; M lineage; Coelomocyte; Asymmetry; C; elegans; HELIX TRANSCRIPTION FACTORS; CAENORHABDITIS-ELEGANS; TGF-BETA; POSTEMBRYONIC MESODERM; CARDIOVASCULAR DEVELOPMENT; AFFINITY PURIFICATION; CIONA-INTESTINALIS; GENETIC-ANALYSIS; GUT DEVELOPMENT; COATED-PIT;
D O I
10.1242/dev.048496
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Forkhead transcription factors play crucial and diverse roles in mesoderm development. In particular, FoxF and FoxC genes are, respectively, involved in the development of visceral/splanchnic mesoderm and non-visceral mesoderm in coelomate animals. Here, we show at single-cell resolution that, in the pseudocoelomate nematode C. elegans, the single FoxF/FoxC transcription factor LET-381 functions in a feed-forward mechanism in the specification and differentiation of the non-muscle mesodermal cells, the coelomocytes (CCs). LET-381/FoxF directly activates the CC specification factor, the Six2 homeodomain protein CEH-34, and functions cooperatively with CEH-34/Six2 to directly activate genes required for CC differentiation. Our results unify a diverse set of studies on the functions of FoxF/FoxC factors and provide a model for how FoxF/FoxC factors function during mesoderm development.
引用
收藏
页码:1451 / 1460
页数:10
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