| Literature DB >> 30661985 |
Daisy A Robinton1, Jérome Chal2, Edroaldo Lummertz da Rocha3, Areum Han1, Alena V Yermalovich1, Masayuki Oginuma2, Thorsten M Schlaeger4, Patricia Sousa1, Antony Rodriguez5, Achia Urbach6, Olivier Pourquié2, George Q Daley7.
Abstract
The heterochronic genes Lin28a/b and let-7 regulate invertebrate development, but their functions in patterning the mammalian body plan remain unexplored. Here, we describe how Lin28/let-7 influence caudal vertebrae number during body axis formation. We found that FoxD1-driven overexpression of Lin28a strikingly increased caudal vertebrae number and tail bud cell proliferation, whereas its knockout did the opposite. Lin28a overexpression downregulated the neural marker Sox2, causing a pro-mesodermal phenotype with a decreased proportion of neural tissue relative to nascent mesoderm. Manipulating Lin28a and let-7 led to opposite effects, and manipulating Lin28a's paralog, LIN28B caused similar yet distinct phenotypes. These findings suggest that Lin28/let-7 play a role in the regulation of tail length through heterochrony of the body plan. We propose that the Lin28/let-7 pathway controls the pool of caudal progenitors during tail development, promoting their self-renewal and balancing neural versus mesodermal cell fate decisions.Entities:
Keywords: Lin28; Sox2; body axis elongation; body plan; cell fate; development; heterochrony; let-7 miRNA; somitogenesis; tail bud
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Year: 2019 PMID: 30661985 DOI: 10.1016/j.devcel.2018.12.016
Source DB: PubMed Journal: Dev Cell ISSN: 1534-5807 Impact factor: 12.270