FGF-Regulated ETV Transcription Factors Control FGF-SHH Feedback Loop in Lung Branching

被引:78
|
作者
Herriges, John C. [1 ]
Verheyden, Jamie M. [1 ]
Zhang, Zhen [1 ,2 ]
Sui, Pengfei
Zhang, Ying [3 ]
Anderson, Matthew J. [3 ]
Swing, Deborah A. [4 ]
Zhang, Yan [1 ]
Lewandoski, Mark [3 ]
Sun, Xin [1 ]
机构
[1] Univ Wisconsin, Genet Lab, Madison, WI 53706 USA
[2] Genentech Inc, Dept Physiol Chem, San Francisco, CA 94080 USA
[3] NCI, Canc & Dev Biol Lab, Frederick, MD 21702 USA
[4] NCI, Mouse Canc Genet Program, Frederick, MD 21702 USA
基金
美国国家卫生研究院;
关键词
MOUSE EMBRYONIC LUNG; SONIC-HEDGEHOG; MORPHOGENESIS; EXPRESSION; LIMB; MECHANISMS; GROWTH; GENE; ORGANOGENESIS; PROGENITORS;
D O I
10.1016/j.devcel.2015.10.006
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
The mammalian lung forms its elaborate tree-like structure following a largely stereotypical branching sequence. While a number of genes have been identified to play essential roles in lung branching, what coordinates the choice between branch growth and new branch formation has not been elucidated. Here we show that loss of FGF-activated transcription factor genes, Etv4 and Etv5 (collectively Etv), led to prolonged branch tip growth and delayed new branch formation. Unexpectedly, this phenotype is more similar to mutants with increased rather than decreased FGF activity. Indeed, an increased Fgf10 expression is observed, and reducing Fgf10 dosage can attenuate the Etv mutant phenotype. Further evidence indicates that ETV inhibits Fgf10 via directly promoting Shh expression. SHH in turn inhibits local Fgf10 expression and redirects growth, thereby initiating new branches. Together, our findings establish EN as a key node in the FGF-ETV-SHH inhibitory feedback loop that dictates branching periodicity.
引用
收藏
页码:322 / 332
页数:11
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