Worniu, a snail family zinc-finger protein, is required for brain development in Drosophila

被引:18
作者
Ashraf, SI
Ganguly, A
Roote, J
Ip, YT
机构
[1] Univ Massachusetts, Sch Med, Program Mol Med, Worcester, MA 01605 USA
[2] Univ Massachusetts, Sch Med, Dept Cell Biol, Worcester, MA 01605 USA
[3] Univ Cambridge, Dept Genet, Cambridge CB2 3EH, England
[4] Univ Massachusetts, Sch Med, Dept Mol Genet & Microbiol, Worcester, MA 01605 USA
[5] Univ Massachusetts, Sch Med, Program Cell Dynam, Worcester, MA 01605 USA
关键词
Snail; Worniu; zinc fingers; repressors; neuroblasts; brain development;
D O I
10.1002/dvdy.20130
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
The Snail family of zinc-finger transcriptional repressors is essential for morphogenetic cell movements, mesoderm formation, and neurogenesis during embryonic development. These proteins also control cell cycle, cell death, and cancer progression. In Drosophila, three members of this protein family, Snail, Escargot, and Worniu, have essential but redundant functions in asymmetric cell division of neuroblasts. In addition, Snail is critical for early mesoderm formation and Escargot is required for maintaining diploidy in wing imaginal disc cells. In this report, we demonstrate that Worniu plays a role in brain development. We show that alleles of the I(2)35Da complementation group are mutants of worniu. The developing larvae of these mutant alleles fail to shorten their brainstems. The brain phenotype, as well as the lethality, of these mutants can be rescued by worniu transgenes. Moreover, RNAi experiments targeting the worniu transcript show the same nonshortening phenotype in larval brains. worniu is expressed in the neuroblasts of brain hemispheres and ventral ganglions. The results suggest that the loss of Worniu function within the neuroblasts ultimately causes the larval brainstem to fail to go through shortening during development. (C) 2004 Wiley-Liss, Inc.
引用
收藏
页码:379 / 386
页数:8
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