Regulation of XSnail2 expression by rho GTPases

被引:24
作者
Broders-Bondon, Florence
Chesneau, Albert
Romero-Oliva, Francisco
Mazabraud, Andre
Mayor, Roberto
Thiery, Jean Paul
机构
[1] Inst Curie, CNRS, Lab Morphogenese Cellulaire & Progress Tumorale, UMR144, F-75248 Paris 05, France
[2] Univ Paris 11, Lab Transgenese & Genet Amphibiens, CNRS, UMR8080,IBAIC, Orsay, France
[3] UCL, Dept Anat & Dev Biol, London WC1E 6BT, England
基金
英国医学研究理事会;
关键词
neural crest; XSnail2; promoter; induction; Rho GTPases; Xenopus laevis;
D O I
10.1002/dvdy.21273
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
We analyzed the effects of Rho GTPases on XSnail2 expression during neural crest (N-) ontogeny in Xenopus laevis embryos. The ectopic expression of both dominant-negative (N-) and constitutively active (V-) Rho GTPase mutants after RNA or DNA microinjection disrupted the endogenous expression of XSnail2, XFoxD3, and XSnaill. V14RhoA and N17Racl were inhibitory, whereas N19RhoA and V12Racl increased NC marker gene expression. In reporter assays using a XSnail2 promoter-green fluorescent protein (GFP) construct (alpha 700BA-GFP), the ectopic expression of V14RhoA, N17Rac1, or the Rac1 inhibitor NSC 23766 decreased reporter expression in NC-neural plate, whereas N19RhoA or the RhoA inhibitor Y27632 and V12Rac1 enhanced it. Similarly, transgenic embryos expressing Rho GTPase mutants and GFP under control of the alpha 700BA promoter displayed variations similar to those observed for ectopic RNA and DNA expression. These results show that Rho GTPases can regulate the expression of XSnail2 during NC ontogeny.
引用
收藏
页码:2555 / 2566
页数:12
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