Literature DB >> 17381276

Misexpression of the Caenorhabditis elegans miRNA let-7 is sufficient to drive developmental programs.

G D Hayes1, G Ruvkun.   

Abstract

The Caenorhabditis elegans microRNAs (miRNAs) lin-4 and let-7 promote transitions between stage-specific events in development by down-regulating the translation of their target genes. Expression of let-7 is required at the fourth larval stage for the proper transition from larval to differentiated, adult fates in the hypodermis; however, it was not known whether expression of let-7 is sufficient to specify these adult fates. To test this, we created fusion genes between lin-4 and let-7 that direct the expression of let-7 two stages early, at the L2 stage. We find that animals bearing the fusion genes show precocious adult development at the L4 stage, indicating that temporal misexpression of let-7 is sufficient to direct the larval-to-adult transition. Additionally, an RNA interference (RNAi)-based screen for enhancers of the precocious phenotype identified the period ortholog lin-42, among other genes, which are candidate modulators of the effects of let-7 expression. let-7 is conserved throughout bilaterian phylogeny, and orthologs of its targets have roles in vertebrate development, suggesting the importance of understanding how let-7 promotes terminal differentiation in C. elegans and other organisms.

Entities:  

Mesh:

Substances:

Year:  2006        PMID: 17381276     DOI: 10.1101/sqb.2006.71.018

Source DB:  PubMed          Journal:  Cold Spring Harb Symp Quant Biol        ISSN: 0091-7451


  17 in total

1.  Temporal regulation of metamorphic processes in Drosophila by the let-7 and miR-125 heterochronic microRNAs.

Authors:  Elizabeth E Caygill; Laura A Johnston
Journal:  Curr Biol       Date:  2008-06-19       Impact factor: 10.834

Review 2.  Nuclear hormone receptors in nematodes: evolution and function.

Authors:  Stefan Taubert; Jordan D Ward; Keith R Yamamoto
Journal:  Mol Cell Endocrinol       Date:  2010-05-10       Impact factor: 4.102

3.  Transgene-mediated cosuppression and RNA interference enhance germ-line apoptosis in Caenorhabditis elegans.

Authors:  Adele Adamo; Alexander Woglar; Nicola Silva; Alexandra Penkner; Verena Jantsch; Adriana La Volpe
Journal:  Proc Natl Acad Sci U S A       Date:  2012-02-13       Impact factor: 11.205

4.  The Caenorhabditis elegans SOMI-1 zinc finger protein and SWI/SNF promote regulation of development by the mir-84 microRNA.

Authors:  Gabriel D Hayes; Christian G Riedel; Gary Ruvkun
Journal:  Genes Dev       Date:  2011-10-01       Impact factor: 11.361

5.  Regulation of lin-4 miRNA expression, organismal growth and development by a conserved RNA binding protein in C. elegans.

Authors:  John R Bracht; Priscilla M Van Wynsberghe; Vanessa Mondol; Amy E Pasquinelli
Journal:  Dev Biol       Date:  2010-10-16       Impact factor: 3.582

6.  Transcription of the C. elegans let-7 microRNA is temporally regulated by one of its targets, hbl-1.

Authors:  Sarah F Roush; Frank J Slack
Journal:  Dev Biol       Date:  2009-07-21       Impact factor: 3.582

Review 7.  An elegant miRror: microRNAs in stem cells, developmental timing and cancer.

Authors:  Rachael A Nimmo; Frank J Slack
Journal:  Chromosoma       Date:  2009-04-03       Impact factor: 4.316

8.  Makorin ortholog LEP-2 regulates LIN-28 stability to promote the juvenile-to-adult transition in Caenorhabditis elegans.

Authors:  R Antonio Herrera; Karin Kiontke; David H A Fitch
Journal:  Development       Date:  2016-01-25       Impact factor: 6.868

9.  Developmental timing: let-7 function conserved through evolution.

Authors:  Jason M Tennessen; Carl S Thummel
Journal:  Curr Biol       Date:  2008-08-26       Impact factor: 10.834

10.  The Period protein homolog LIN-42 negatively regulates microRNA biogenesis in C. elegans.

Authors:  Priscilla M Van Wynsberghe; Emily F Finnegan; Thomas Stark; Evan P Angelus; Kathryn E Homan; Gene W Yeo; Amy E Pasquinelli
Journal:  Dev Biol       Date:  2014-03-31       Impact factor: 3.582

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.