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Life Sci Alliance. 2019 Mar 25;2(2). pii: e201900335. doi: 10.26508/lsa.201900335. Print 2019 Apr.

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

Author information

1
Friedrich Miescher Institute for Biomedical Research, Basel, Switzerland.
2
University of Basel, Basel, Switzerland.
3
Friedrich Miescher Institute for Biomedical Research, Basel, Switzerland helge.grosshans@fmi.ch.

Abstract

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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