VAL genes regulate vegetative phase change via miR156-dependent and independent mechanisms.

How organisms control when to transition between different stages of development is a key question in biology. In plants, epigenetic silencing by Polycomb repressive complex 1 (PRC1) and PRC2 plays a crucial role in promoting developmental transitions, including from juvenile-to-adult phases of vege...

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Main Authors: Jim P Fouracre, Jia He, Victoria J Chen, Simone Sidoli, R Scott Poethig
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2021-06-01
Series:PLoS Genetics
Online Access:https://doi.org/10.1371/journal.pgen.1009626
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spelling doaj-ae426931fb0643db9ba84ce57c525a4f2021-07-25T04:31:09ZengPublic Library of Science (PLoS)PLoS Genetics1553-73901553-74042021-06-01176e100962610.1371/journal.pgen.1009626VAL genes regulate vegetative phase change via miR156-dependent and independent mechanisms.Jim P FouracreJia HeVictoria J ChenSimone SidoliR Scott PoethigHow organisms control when to transition between different stages of development is a key question in biology. In plants, epigenetic silencing by Polycomb repressive complex 1 (PRC1) and PRC2 plays a crucial role in promoting developmental transitions, including from juvenile-to-adult phases of vegetative growth. PRC1/2 are known to repress the master regulator of vegetative phase change, miR156, leading to the transition to adult growth, but how this process is regulated temporally is unknown. Here we investigate whether transcription factors in the VIVIPAROUS/ABI3-LIKE (VAL) gene family provide the temporal signal for the epigenetic repression of miR156. Exploiting a novel val1 allele, we found that VAL1 and VAL2 redundantly regulate vegetative phase change by controlling the overall level, rather than temporal dynamics, of miR156 expression. Furthermore, we discovered that VAL1 and VAL2 also act independently of miR156 to control this important developmental transition. In combination, our results highlight the complexity of temporal regulation in plants.https://doi.org/10.1371/journal.pgen.1009626
collection DOAJ
language English
format Article
sources DOAJ
author Jim P Fouracre
Jia He
Victoria J Chen
Simone Sidoli
R Scott Poethig
spellingShingle Jim P Fouracre
Jia He
Victoria J Chen
Simone Sidoli
R Scott Poethig
VAL genes regulate vegetative phase change via miR156-dependent and independent mechanisms.
PLoS Genetics
author_facet Jim P Fouracre
Jia He
Victoria J Chen
Simone Sidoli
R Scott Poethig
author_sort Jim P Fouracre
title VAL genes regulate vegetative phase change via miR156-dependent and independent mechanisms.
title_short VAL genes regulate vegetative phase change via miR156-dependent and independent mechanisms.
title_full VAL genes regulate vegetative phase change via miR156-dependent and independent mechanisms.
title_fullStr VAL genes regulate vegetative phase change via miR156-dependent and independent mechanisms.
title_full_unstemmed VAL genes regulate vegetative phase change via miR156-dependent and independent mechanisms.
title_sort val genes regulate vegetative phase change via mir156-dependent and independent mechanisms.
publisher Public Library of Science (PLoS)
series PLoS Genetics
issn 1553-7390
1553-7404
publishDate 2021-06-01
description How organisms control when to transition between different stages of development is a key question in biology. In plants, epigenetic silencing by Polycomb repressive complex 1 (PRC1) and PRC2 plays a crucial role in promoting developmental transitions, including from juvenile-to-adult phases of vegetative growth. PRC1/2 are known to repress the master regulator of vegetative phase change, miR156, leading to the transition to adult growth, but how this process is regulated temporally is unknown. Here we investigate whether transcription factors in the VIVIPAROUS/ABI3-LIKE (VAL) gene family provide the temporal signal for the epigenetic repression of miR156. Exploiting a novel val1 allele, we found that VAL1 and VAL2 redundantly regulate vegetative phase change by controlling the overall level, rather than temporal dynamics, of miR156 expression. Furthermore, we discovered that VAL1 and VAL2 also act independently of miR156 to control this important developmental transition. In combination, our results highlight the complexity of temporal regulation in plants.
url https://doi.org/10.1371/journal.pgen.1009626
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