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let-7 coordinates the transition to adulthood through a single primary and four secondary targets

The juvenile-to-adult (J/A) transition, or puberty, is a period of extensive changes of animal body morphology and function. The onset of puberty is genetically controlled, and the let-7 miRNA temporally regulates J/A transition events in nematodes and mammals. Here, we uncover the targets and downs...

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Autores principales: Aeschimann, Florian, Neagu, Anca, Rausch, Magdalene, Großhans, Helge
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Life Science Alliance LLC 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6435043/
https://www.ncbi.nlm.nih.gov/pubmed/30910805
http://dx.doi.org/10.26508/lsa.201900335
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author Aeschimann, Florian
Neagu, Anca
Rausch, Magdalene
Großhans, Helge
author_facet Aeschimann, Florian
Neagu, Anca
Rausch, Magdalene
Großhans, Helge
author_sort Aeschimann, Florian
collection PubMed
description The juvenile-to-adult (J/A) transition, or puberty, is a period of extensive changes of animal body morphology and function. The onset of puberty is genetically controlled, and the let-7 miRNA temporally regulates J/A transition events in nematodes and mammals. Here, we uncover the targets and downstream pathways through which Caenorhabditis elegans let-7 controls male and female sexual organ morphogenesis and skin progenitor cell fates. We find that let-7 directs all three processes by silencing a single target, the post-transcriptional regulator lin-41. In turn, the RNA-binding protein LIN41/TRIM71 regulates these processes by silencing only four target mRNAs. Thus, by silencing LIN41, let-7 activates LIN-29a and MAB-10 (an early growth response-type transcription factor and its NAB1/2-orthologous cofactor, respectively) to terminate progenitor cell self-renewal and to promote vulval integrity. By contrast, let-7 promotes development of the male sexual organ by up-regulating DMD-3 and MAB-3, two Doublesex/MAB-3 domain–containing transcription factors. Our results provide mechanistic insight into how a linear chain of post-transcriptional regulators diverges in the control of a small set of transcriptional regulators to achieve a coordinated J/A transition.
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spelling pubmed-64350432019-04-01 let-7 coordinates the transition to adulthood through a single primary and four secondary targets Aeschimann, Florian Neagu, Anca Rausch, Magdalene Großhans, Helge Life Sci Alliance Research Articles The juvenile-to-adult (J/A) transition, or puberty, is a period of extensive changes of animal body morphology and function. The onset of puberty is genetically controlled, and the let-7 miRNA temporally regulates J/A transition events in nematodes and mammals. Here, we uncover the targets and downstream pathways through which Caenorhabditis elegans let-7 controls male and female sexual organ morphogenesis and skin progenitor cell fates. We find that let-7 directs all three processes by silencing a single target, the post-transcriptional regulator lin-41. In turn, the RNA-binding protein LIN41/TRIM71 regulates these processes by silencing only four target mRNAs. Thus, by silencing LIN41, let-7 activates LIN-29a and MAB-10 (an early growth response-type transcription factor and its NAB1/2-orthologous cofactor, respectively) to terminate progenitor cell self-renewal and to promote vulval integrity. By contrast, let-7 promotes development of the male sexual organ by up-regulating DMD-3 and MAB-3, two Doublesex/MAB-3 domain–containing transcription factors. Our results provide mechanistic insight into how a linear chain of post-transcriptional regulators diverges in the control of a small set of transcriptional regulators to achieve a coordinated J/A transition. Life Science Alliance LLC 2019-03-25 /pmc/articles/PMC6435043/ /pubmed/30910805 http://dx.doi.org/10.26508/lsa.201900335 Text en © 2019 Aeschimann et al. https://creativecommons.org/licenses/by/4.0/This article is available under a Creative Commons License (Attribution 4.0 International, as described at https://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Articles
Aeschimann, Florian
Neagu, Anca
Rausch, Magdalene
Großhans, Helge
let-7 coordinates the transition to adulthood through a single primary and four secondary targets
title let-7 coordinates the transition to adulthood through a single primary and four secondary targets
title_full let-7 coordinates the transition to adulthood through a single primary and four secondary targets
title_fullStr let-7 coordinates the transition to adulthood through a single primary and four secondary targets
title_full_unstemmed let-7 coordinates the transition to adulthood through a single primary and four secondary targets
title_short let-7 coordinates the transition to adulthood through a single primary and four secondary targets
title_sort let-7 coordinates the transition to adulthood through a single primary and four secondary targets
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6435043/
https://www.ncbi.nlm.nih.gov/pubmed/30910805
http://dx.doi.org/10.26508/lsa.201900335
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