Chromatin retained MUSHER lncRNA integrates ABA and DOG1 signalling pathways to enhance Arabidopsis seeds dormancy
Many plant lncRNAs regulate gene expression by binding to chromatin, but how they are retained at the target loci is unclear. We identify a chromatin-localized lncRNA - MUSHER , which activates two parallel regulatory pathways to increase Arabidopsis seed dormancy. MUSHER is upregulated in response...
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Published in | Nature communications Vol. 16; no. 1; pp. 7545 - 18 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
14.08.2025
Nature Publishing Group Nature Portfolio |
Subjects | |
Online Access | Get full text |
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Summary: | Many plant lncRNAs regulate gene expression by binding to chromatin, but how they are retained at the target
loci
is unclear. We identify a chromatin-localized lncRNA -
MUSHER
, which activates two parallel regulatory pathways to increase Arabidopsis seed dormancy.
MUSHER
is upregulated in response to high temperatures, contributing to the induction of secondary dormancy. It promotes
DOG1
expression by recruitment of the CPSF complex to enhance the proximal cleavage and polyadenylation at the
DOG1
transcript. It also increases ABA sensitivity in seeds by activating
PIR1
gene transcription. These genes, located on different chromosomes, are both bound by
MUSHER
, despite lacking sequence homology. The chromatin association of
MUSHER
enables the integration of the DOG1- and ABA pathways to adjust seed germination timing. Additionally,
MUSHER
and other lncRNAs interact with U1 snRNP, which is required for their chromatin localisation, revealing a role for U1 snRNP in plants.
Here the authors show that
MUSHER
lncRNA enhances Arabidopsis seed dormancy by integrating the ABA and DOG1 pathways. Chromatin retention of
MUSHER
and all other lncRNAs tested is mediated by U1 snRNP. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 |
ISSN: | 2041-1723 2041-1723 |
DOI: | 10.1038/s41467-025-62991-5 |