Fgf-dependent depletion of microRNA-133 promotes appendage regeneration in zebrafish

被引:113
作者
Yin, Viravuth P. [1 ]
Thomson, J. Michael [2 ]
Thummel, Ryan [3 ,4 ]
Hyde, David R. [3 ,4 ]
Hammond, Scott M. [2 ]
Poss, Kenneth D. [1 ]
机构
[1] Duke Univ, Med Ctr, Dept Cell Biol, Durham, NC 27710 USA
[2] Univ N Carolina, Dept Cell & Dev Biol, Chapel Hill, NC 27599 USA
[3] Univ Notre Dame, Ctr Zebrafish Res, Notre Dame, IN 46556 USA
[4] Univ Notre Dame, Dept Biol Sci, Notre Dame, IN 46556 USA
关键词
zebrafish; fin; regeneration; miR-133; Fgf; Mps1;
D O I
10.1101/gad.1641808
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Appendage regeneration is defined by rapid changes in gene expression that achieve dramatic developmental effects, suggesting involvement of microRNAs (miRNAs). Here, we find dynamic regulation of many miRNAs during zebrafish fin regeneration. In particular, miR-133 levels are high in uninjured fins but low during regeneration. When regeneration was blocked by Fibroblast growth factor (Fgf) receptor inhibition, high miR-133 levels were quickly restored. Experimentally increasing amounts of miR-133 attenuated fin regeneration. Conversely, miR-133 antagonism during Fgf receptor inhibition accelerated regeneration through increased proliferation within the regeneration blastema. The Mps1 kinase, an established positive regulator of blastemal proliferation, is an in vivo target of miR-133. Our findings identify miRNA depletion as a new regulatory mechanism for complex tissue regeneration.
引用
收藏
页码:728 / 733
页数:6
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