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Gene duplication at the Fascicled ear1 locus controls the fate of inflorescence meristem cells in maize

Plant meristems are self-renewing groups of pluripotent stem cells that produce lateral organs in a stereotypical pattern. Of interest is how the radially symmetrical meristem produces laminar lateral organs. Both the male and female inflorescence meristems of the dominant Fascicled ear (Fas1) mutan...

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Autores principales: Du, Yanfang, Lunde, China, Li, Yunfu, Jackson, David, Hake, Sarah, Zhang, Zuxin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: National Academy of Sciences 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7896288/
https://www.ncbi.nlm.nih.gov/pubmed/33579824
http://dx.doi.org/10.1073/pnas.2019218118
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author Du, Yanfang
Lunde, China
Li, Yunfu
Jackson, David
Hake, Sarah
Zhang, Zuxin
author_facet Du, Yanfang
Lunde, China
Li, Yunfu
Jackson, David
Hake, Sarah
Zhang, Zuxin
author_sort Du, Yanfang
collection PubMed
description Plant meristems are self-renewing groups of pluripotent stem cells that produce lateral organs in a stereotypical pattern. Of interest is how the radially symmetrical meristem produces laminar lateral organs. Both the male and female inflorescence meristems of the dominant Fascicled ear (Fas1) mutant fail to grow as a single point and instead show deep branching. Positional cloning of two independent Fas1 alleles identified an ∼160 kb region containing two floral genes, the MADS-box gene, zmm8, and the YABBY gene, drooping leaf2 (drl2). Both genes are duplicated within the Fas1 locus and spatiotemporally misexpressed in the mutant inflorescence meristems. Increased zmm8 expression alone does not affect inflorescence development; however, combined misexpression of zmm8, drl2, and their syntenic paralogs zmm14 and drl1, perturbs meristem organization. We hypothesize that misexpression of the floral genes in the inflorescence and their potential interaction cause ectopic activation of a laminar program, thereby disrupting signaling necessary for maintenance of radially symmetrical inflorescence meristems. Consistent with this hypothesis, RNA sequencing and in situ analysis reveal altered expression patterns of genes that define distinct zones of the meristem and developing leaf. Our findings highlight the importance of strict spatiotemporal patterns of expression for both zmm8 and drl2 and provide an example of phenotypes arising from tandem gene duplications.
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spelling pubmed-78962882021-02-24 Gene duplication at the Fascicled ear1 locus controls the fate of inflorescence meristem cells in maize Du, Yanfang Lunde, China Li, Yunfu Jackson, David Hake, Sarah Zhang, Zuxin Proc Natl Acad Sci U S A Biological Sciences Plant meristems are self-renewing groups of pluripotent stem cells that produce lateral organs in a stereotypical pattern. Of interest is how the radially symmetrical meristem produces laminar lateral organs. Both the male and female inflorescence meristems of the dominant Fascicled ear (Fas1) mutant fail to grow as a single point and instead show deep branching. Positional cloning of two independent Fas1 alleles identified an ∼160 kb region containing two floral genes, the MADS-box gene, zmm8, and the YABBY gene, drooping leaf2 (drl2). Both genes are duplicated within the Fas1 locus and spatiotemporally misexpressed in the mutant inflorescence meristems. Increased zmm8 expression alone does not affect inflorescence development; however, combined misexpression of zmm8, drl2, and their syntenic paralogs zmm14 and drl1, perturbs meristem organization. We hypothesize that misexpression of the floral genes in the inflorescence and their potential interaction cause ectopic activation of a laminar program, thereby disrupting signaling necessary for maintenance of radially symmetrical inflorescence meristems. Consistent with this hypothesis, RNA sequencing and in situ analysis reveal altered expression patterns of genes that define distinct zones of the meristem and developing leaf. Our findings highlight the importance of strict spatiotemporal patterns of expression for both zmm8 and drl2 and provide an example of phenotypes arising from tandem gene duplications. National Academy of Sciences 2021-02-16 2021-02-12 /pmc/articles/PMC7896288/ /pubmed/33579824 http://dx.doi.org/10.1073/pnas.2019218118 Text en Copyright © 2021 the Author(s). Published by PNAS. https://creativecommons.org/licenses/by-nc-nd/4.0/ https://creativecommons.org/licenses/by-nc-nd/4.0/This open access article is distributed under Creative Commons Attribution-NonCommercial-NoDerivatives License 4.0 (CC BY-NC-ND) (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Biological Sciences
Du, Yanfang
Lunde, China
Li, Yunfu
Jackson, David
Hake, Sarah
Zhang, Zuxin
Gene duplication at the Fascicled ear1 locus controls the fate of inflorescence meristem cells in maize
title Gene duplication at the Fascicled ear1 locus controls the fate of inflorescence meristem cells in maize
title_full Gene duplication at the Fascicled ear1 locus controls the fate of inflorescence meristem cells in maize
title_fullStr Gene duplication at the Fascicled ear1 locus controls the fate of inflorescence meristem cells in maize
title_full_unstemmed Gene duplication at the Fascicled ear1 locus controls the fate of inflorescence meristem cells in maize
title_short Gene duplication at the Fascicled ear1 locus controls the fate of inflorescence meristem cells in maize
title_sort gene duplication at the fascicled ear1 locus controls the fate of inflorescence meristem cells in maize
topic Biological Sciences
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7896288/
https://www.ncbi.nlm.nih.gov/pubmed/33579824
http://dx.doi.org/10.1073/pnas.2019218118
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