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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2021-06-01
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Series: | PLoS Genetics |
Online Access: | https://doi.org/10.1371/journal.pgen.1009626 |
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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 |
work_keys_str_mv |
AT jimpfouracre valgenesregulatevegetativephasechangeviamir156dependentandindependentmechanisms AT jiahe valgenesregulatevegetativephasechangeviamir156dependentandindependentmechanisms AT victoriajchen valgenesregulatevegetativephasechangeviamir156dependentandindependentmechanisms AT simonesidoli valgenesregulatevegetativephasechangeviamir156dependentandindependentmechanisms AT rscottpoethig valgenesregulatevegetativephasechangeviamir156dependentandindependentmechanisms |
_version_ |
1721284037456166912 |