Animal models for studying neural crest development: is the mouse different?

被引：61

作者：

Barriga, Elias H. ^{[1
]}

Trainor, Paul A. ^{[2
,3
]}

Bronner, Marianne ^{[4
]}

Mayor, Roberto ^{[1
]}

机构：

[1] UCL, Dept Cell & Dev Biol, London WC1E 6BT, England

[2] Stowers Inst Med Res, Kansas City, MO 64110 USA

[3] Univ Kansas, Med Ctr, Dept Anat & Cell Biol, Kansas City, KS 66160 USA

[4] CALTECH, Div Biol, Pasadena, CA 91125 USA

来源：

DEVELOPMENT | 2015年 / 142卷 / 09期

基金：

英国医学研究理事会; 英国惠康基金; 英国生物技术与生命科学研究理事会;

关键词：

Neural crest; Mouse; Zebrafish; Xenopus; Chicken; Gene knockout; TRANSCRIPTION FACTOR AP-2; GENE REGULATORY NETWORK; CARDIAC OUTFLOW TRACT; RETINOIC ACID; N-CADHERIN; ANTEROPOSTERIOR AXIS; ZEBRAFISH FOXD3; XENOPUS EMBRYOS; CELL POLARITY; DANIO-RERIO;

D O I：

10.1242/dev.121590

中图分类号：

Q [生物科学];

学科分类号：

07 ; 0710 ; 09 ;

摘要：

The neural crest is a uniquely vertebrate cell type and has been well studied in a number of model systems. Zebrafish, Xenopus and chick embryos largely show consistent requirements for specific genes in early steps of neural crest development. By contrast, knockouts of homologous genes in the mouse often do not exhibit comparable early neural crest phenotypes. In this Spotlight article, we discuss these species-specific differences, suggest possible explanations for the divergent phenotypes in mouse and urge the community to consider these issues and the need for further research in complementary systems.

引用

页码：1555 / 1560

页数：6

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