Expression and function of the Ets transcription factor pea3 during formation of zebrafish pronephros

被引:1
|
作者
Chen, Qiuxia [1 ,2 ]
Huang, Songming [1 ,2 ]
Zhao, Qingshun [3 ]
Chen, Ronghua [2 ]
Zhang, Aihua [1 ,2 ]
机构
[1] Nanjing Med Univ, Nanjing Childrens Hosp, Dept Nephrol, Nanjing 210008, Peoples R China
[2] Nanjing Med Univ, Inst Pediat, Nanjing, Peoples R China
[3] Nanjing Univ, Model Anim Res Ctr, MOE Key Lab Model Anim Dis Study, Nanjing, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
pea3; Zebrafish; Pronephros; Nephrogenesis; erm; wt1a; EARLY KIDNEY DEVELOPMENT; BRANCHING MORPHOGENESIS; NEUROTROPHIC FACTOR; MOLECULAR-CLONING; MOUSE; GENE; DIFFERENTIATION; ACTIVATION; FAMILY; MEMBER;
D O I
10.1007/s00467-010-1713-9
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Polyomavirus enhancer activator 3 (Pea3), belonging to the PEA3 subfamily of Ets transcription factors, is essential for certain organogenesis in mammals. Previously, we found that pea3 correlated with wt1 expression and may contribute to nephrogenesis in rats. Here, we observed that pea3 was mainly expressed in the zebrafish pronephric glomerulus. We further performed functional analyses by in situ hybridization of pea3 in zebrafish embryos after pea3 messenger RNA (mRNA) overexpression and inhibition of double-target genes (pea3 and erm, another member of the PEA3 subfamily) by antisense morpholino-oligonucleotides (MO). Overexpression of pea3 induced abnormal pronephrogenesis. However, MO-pea3 coinjected with MO-erm, but not alone, inhibited zebrafish pronephros development, and these defects were rescued by overexpression of the zebrafish who gene. Thus, pea3 and erm are required for zebralish pronephrogenesis and can functionally complement each other, and the wt1a gene may be one of their downstream targets.
引用
收藏
页码:391 / 400
页数:10
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