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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Life Science Alliance LLC
2019
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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. |
format | Online Article Text |
id | pubmed-6435043 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Life Science Alliance LLC |
record_format | MEDLINE/PubMed |
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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