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ARR17 controls dioecy in Populus by repressing B-class MADS-box gene expression

The number of dioecious species for which the genetic basis of sex determination has been resolved is rapidly increasing. Nevertheless, the molecular mechanisms downstream of the sex determinants remain largely elusive. Here, by RNA-sequencing early-flowering isogenic aspen (Populus tremula) lines d...

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Autores principales: Leite Montalvão, Ana P., Kersten, Birgit, Kim, Gihwan, Fladung, Matthias, Müller, Niels A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8935312/
https://www.ncbi.nlm.nih.gov/pubmed/35306887
http://dx.doi.org/10.1098/rstb.2021.0217
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author Leite Montalvão, Ana P.
Kersten, Birgit
Kim, Gihwan
Fladung, Matthias
Müller, Niels A.
author_facet Leite Montalvão, Ana P.
Kersten, Birgit
Kim, Gihwan
Fladung, Matthias
Müller, Niels A.
author_sort Leite Montalvão, Ana P.
collection PubMed
description The number of dioecious species for which the genetic basis of sex determination has been resolved is rapidly increasing. Nevertheless, the molecular mechanisms downstream of the sex determinants remain largely elusive. Here, by RNA-sequencing early-flowering isogenic aspen (Populus tremula) lines differing exclusively for the sex switch gene ARR17, we show that a narrowly defined genetic network controls differential development of female and male flowers. Although ARR17 encodes a type-A response regulator supposedly involved in cytokinin (CK) hormone signalling, clustered regularly interspaced short palindromic repeats (CRISPR)-Cas9-mediated arr17 knockout only affected the expression of a strikingly small number of genes, indicating a specific role in the regulation of floral development rather than a generic function in hormone signalling. Notably, the UNUSUAL FLORAL ORGANS (UFO) gene, encoding an F-box protein acting as a transcriptional cofactor with LEAFY (LFY) to activate B-class MADS-box gene expression, and the B-class gene PISTILLATA (PI), necessary for male floral organ development, were strongly de-repressed in the arr17 CRISPR mutants. Our data highlight a CK-independent role of the poplar response regulator ARR17 and further emphasize the minimal differences between female and male individuals. This article is part of the theme issue ‘Sex determination and sex chromosome evolution in land plants’.
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spelling pubmed-89353122022-03-25 ARR17 controls dioecy in Populus by repressing B-class MADS-box gene expression Leite Montalvão, Ana P. Kersten, Birgit Kim, Gihwan Fladung, Matthias Müller, Niels A. Philos Trans R Soc Lond B Biol Sci Articles The number of dioecious species for which the genetic basis of sex determination has been resolved is rapidly increasing. Nevertheless, the molecular mechanisms downstream of the sex determinants remain largely elusive. Here, by RNA-sequencing early-flowering isogenic aspen (Populus tremula) lines differing exclusively for the sex switch gene ARR17, we show that a narrowly defined genetic network controls differential development of female and male flowers. Although ARR17 encodes a type-A response regulator supposedly involved in cytokinin (CK) hormone signalling, clustered regularly interspaced short palindromic repeats (CRISPR)-Cas9-mediated arr17 knockout only affected the expression of a strikingly small number of genes, indicating a specific role in the regulation of floral development rather than a generic function in hormone signalling. Notably, the UNUSUAL FLORAL ORGANS (UFO) gene, encoding an F-box protein acting as a transcriptional cofactor with LEAFY (LFY) to activate B-class MADS-box gene expression, and the B-class gene PISTILLATA (PI), necessary for male floral organ development, were strongly de-repressed in the arr17 CRISPR mutants. Our data highlight a CK-independent role of the poplar response regulator ARR17 and further emphasize the minimal differences between female and male individuals. This article is part of the theme issue ‘Sex determination and sex chromosome evolution in land plants’. The Royal Society 2022-05-09 2022-03-21 /pmc/articles/PMC8935312/ /pubmed/35306887 http://dx.doi.org/10.1098/rstb.2021.0217 Text en © 2022 The Authors. https://creativecommons.org/licenses/by/4.0/Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, provided the original author and source are credited.
spellingShingle Articles
Leite Montalvão, Ana P.
Kersten, Birgit
Kim, Gihwan
Fladung, Matthias
Müller, Niels A.
ARR17 controls dioecy in Populus by repressing B-class MADS-box gene expression
title ARR17 controls dioecy in Populus by repressing B-class MADS-box gene expression
title_full ARR17 controls dioecy in Populus by repressing B-class MADS-box gene expression
title_fullStr ARR17 controls dioecy in Populus by repressing B-class MADS-box gene expression
title_full_unstemmed ARR17 controls dioecy in Populus by repressing B-class MADS-box gene expression
title_short ARR17 controls dioecy in Populus by repressing B-class MADS-box gene expression
title_sort arr17 controls dioecy in populus by repressing b-class mads-box gene expression
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8935312/
https://www.ncbi.nlm.nih.gov/pubmed/35306887
http://dx.doi.org/10.1098/rstb.2021.0217
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