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Polymerase II-Associated Factor 1 Complex-Regulated FLOWERING LOCUS C -Clade Genes Repress Flowering in Response to Chilling
RNA polymerase II-associated factor 1 complex (PAF1C) regulates the transition from the vegetative to the reproductive phase primarily by modulating the expression of ( ) and [ , also known as ( )] at standard growth temperatures. However, the role of PAF1C in the regulation of flowering time at chi...
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Published in: | Frontiers in plant science 2022-02, Vol.13, p.817356-817356 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | RNA polymerase II-associated factor 1 complex (PAF1C) regulates the transition from the vegetative to the reproductive phase primarily by modulating the expression of
(
) and
[
, also known as
(
)] at standard growth temperatures. However, the role of PAF1C in the regulation of flowering time at chilling temperatures (i.e., cold temperatures that are above freezing) and whether PAF1C affects other
-clade genes (
-
) remains unknown. Here, we showed that
mutants of any of the six known genes that encode components of PAF1C [
,
(
)/
(
),
,
,
, and
] showed temperature-insensitive early flowering across a broad temperature range (10°C-27°C). Flowering of PAF1C-deficient mutants at 10°C was even earlier than that in
,
, and
mutants, suggesting that PAF1C regulates additional factors. Indeed, RNA sequencing (RNA-Seq) of PAF1C-deficient mutants revealed downregulation of
in addition to
and
at both 10 and 23°C. Consistent with the reduced expression of
and the
-clade members
and
, chromatin immunoprecipitation (ChIP)-quantitative PCR assays showed reduced levels of the permissive epigenetic modification H3K4me3/H3K36me3 and increased levels of the repressive modification H3K27me3 at their chromatin. Knocking down
using artificial microRNAs (amiRNAs) in the
background (
) resulted in significantly earlier flowering than
mutants and even earlier than
(
) mutants at 10°C. Wild-type seedlings showed higher accumulation of
and
-clade gene transcripts at 10°C compared to 23°C. Our yeast two-hybrid assays and
co-immunoprecipitation (Co-IP) analyses revealed that MAF2-MAF5 directly interact with the prominent floral repressor SVP. Late flowering caused by
overexpression was almost completely suppressed by the
and
mutations, suggesting that SVP-mediated floral repression required a functional PAF1C. Taken together, our results showed that PAF1C regulates the transcription of
and
-clade genes to modulate temperature-responsive flowering at a broad range of temperatures and that the interaction between SVP and these FLC-clade proteins is important for floral repression. |
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ISSN: | 1664-462X 1664-462X |
DOI: | 10.3389/fpls.2022.817356 |