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AP1G2 Affects Mitotic Cycles of Female and Male Gametophytes in Arabidopsis

During sexual reproduction in flowering plants, haploid spores are formed from meiosis of spore mother cells. The spores then undergo mitosis, develop into female and male gametophytes, and give rise to seeds after fertilization. We identified a female sterile mutant ap1g2-4 from EMS mutagenesis, an...

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Autores principales: Zhou, Yongmei, Fang, Wenqin, Pang, Ziqin, Chen, Li-Yu, Cai, Hanyang, Ain, Noor-Ul-, Chang, Men-Chi, Ming, Ray
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9301471/
https://www.ncbi.nlm.nih.gov/pubmed/35873977
http://dx.doi.org/10.3389/fpls.2022.924417
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author Zhou, Yongmei
Fang, Wenqin
Pang, Ziqin
Chen, Li-Yu
Cai, Hanyang
Ain, Noor-Ul-
Chang, Men-Chi
Ming, Ray
author_facet Zhou, Yongmei
Fang, Wenqin
Pang, Ziqin
Chen, Li-Yu
Cai, Hanyang
Ain, Noor-Ul-
Chang, Men-Chi
Ming, Ray
author_sort Zhou, Yongmei
collection PubMed
description During sexual reproduction in flowering plants, haploid spores are formed from meiosis of spore mother cells. The spores then undergo mitosis, develop into female and male gametophytes, and give rise to seeds after fertilization. We identified a female sterile mutant ap1g2-4 from EMS mutagenesis, and analyses of two T-DNA insertion mutants, ap1g2-1(+/−) and ap1g2-3(−/−), and detected a partial female and male sterility. The ap1g2 mutant gametophyte development was arrested at one nuclear stage. A complementation test using a genomic sequence of AP1G2 with its native promoter restored the function in the three ap1g2 mutant lines. Transcriptome profiling of ap1g2 ovules revealed that four genes encoding clathrin assembly proteins PICALM5A/B and PICALM9A/B, which were involved in endocytosis, were downregulated, which were confirmed to interact with AP1G2 through yeast two-hybrid assays and BIFC analysis. Our result also demonstrated that RALFL4-8-15-19-26 CML16 and several calcium-dependent protein kinases, including CPK14-16-17, were all downregulated in the ovules of ap1g2-1(+/−). Moreover, Ca(2+) concentration was low in impaired gametophytes. Therefore, we proposed that through interaction with PICALM5A/B and PICALM9A/B, AP1G2 may mediate gametogenesis accompanied by Ca(2+) signaling in Arabidopsis. Our findings revealed a crucial role of AP1G2 in female and male gametogenesis in Arabidopsis and enhanced our understanding of the molecular mechanisms underpinning sexual reproduction in flowering plants.
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spelling pubmed-93014712022-07-22 AP1G2 Affects Mitotic Cycles of Female and Male Gametophytes in Arabidopsis Zhou, Yongmei Fang, Wenqin Pang, Ziqin Chen, Li-Yu Cai, Hanyang Ain, Noor-Ul- Chang, Men-Chi Ming, Ray Front Plant Sci Plant Science During sexual reproduction in flowering plants, haploid spores are formed from meiosis of spore mother cells. The spores then undergo mitosis, develop into female and male gametophytes, and give rise to seeds after fertilization. We identified a female sterile mutant ap1g2-4 from EMS mutagenesis, and analyses of two T-DNA insertion mutants, ap1g2-1(+/−) and ap1g2-3(−/−), and detected a partial female and male sterility. The ap1g2 mutant gametophyte development was arrested at one nuclear stage. A complementation test using a genomic sequence of AP1G2 with its native promoter restored the function in the three ap1g2 mutant lines. Transcriptome profiling of ap1g2 ovules revealed that four genes encoding clathrin assembly proteins PICALM5A/B and PICALM9A/B, which were involved in endocytosis, were downregulated, which were confirmed to interact with AP1G2 through yeast two-hybrid assays and BIFC analysis. Our result also demonstrated that RALFL4-8-15-19-26 CML16 and several calcium-dependent protein kinases, including CPK14-16-17, were all downregulated in the ovules of ap1g2-1(+/−). Moreover, Ca(2+) concentration was low in impaired gametophytes. Therefore, we proposed that through interaction with PICALM5A/B and PICALM9A/B, AP1G2 may mediate gametogenesis accompanied by Ca(2+) signaling in Arabidopsis. Our findings revealed a crucial role of AP1G2 in female and male gametogenesis in Arabidopsis and enhanced our understanding of the molecular mechanisms underpinning sexual reproduction in flowering plants. Frontiers Media S.A. 2022-07-07 /pmc/articles/PMC9301471/ /pubmed/35873977 http://dx.doi.org/10.3389/fpls.2022.924417 Text en Copyright © 2022 Zhou, Fang, Pang, Chen, Cai, Ain, Chang and Ming. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Plant Science
Zhou, Yongmei
Fang, Wenqin
Pang, Ziqin
Chen, Li-Yu
Cai, Hanyang
Ain, Noor-Ul-
Chang, Men-Chi
Ming, Ray
AP1G2 Affects Mitotic Cycles of Female and Male Gametophytes in Arabidopsis
title AP1G2 Affects Mitotic Cycles of Female and Male Gametophytes in Arabidopsis
title_full AP1G2 Affects Mitotic Cycles of Female and Male Gametophytes in Arabidopsis
title_fullStr AP1G2 Affects Mitotic Cycles of Female and Male Gametophytes in Arabidopsis
title_full_unstemmed AP1G2 Affects Mitotic Cycles of Female and Male Gametophytes in Arabidopsis
title_short AP1G2 Affects Mitotic Cycles of Female and Male Gametophytes in Arabidopsis
title_sort ap1g2 affects mitotic cycles of female and male gametophytes in arabidopsis
topic Plant Science
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9301471/
https://www.ncbi.nlm.nih.gov/pubmed/35873977
http://dx.doi.org/10.3389/fpls.2022.924417
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