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The cohesin loader SCC2 contains a PHD finger that is required for meiosis in land plants

Cohesin, a multisubunit protein complex, is required for holding sister chromatids together during mitosis and meiosis. The recruitment of cohesin by the sister chromatid cohesion 2/4 (SCC2/4) complex has been extensively studied in Saccharomyces cerevisiae mitosis, but its role in mitosis and meios...

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Autores principales: Wang, Hongkuan, Xu, Wanyue, Sun, Yujin, Lian, Qichao, Wang, Cong, Yu, Chaoyi, He, Chengpeng, Wang, Jun, Ma, Hong, Copenhaver, Gregory P., Wang, Yingxiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7304647/
https://www.ncbi.nlm.nih.gov/pubmed/32516352
http://dx.doi.org/10.1371/journal.pgen.1008849
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author Wang, Hongkuan
Xu, Wanyue
Sun, Yujin
Lian, Qichao
Wang, Cong
Yu, Chaoyi
He, Chengpeng
Wang, Jun
Ma, Hong
Copenhaver, Gregory P.
Wang, Yingxiang
author_facet Wang, Hongkuan
Xu, Wanyue
Sun, Yujin
Lian, Qichao
Wang, Cong
Yu, Chaoyi
He, Chengpeng
Wang, Jun
Ma, Hong
Copenhaver, Gregory P.
Wang, Yingxiang
author_sort Wang, Hongkuan
collection PubMed
description Cohesin, a multisubunit protein complex, is required for holding sister chromatids together during mitosis and meiosis. The recruitment of cohesin by the sister chromatid cohesion 2/4 (SCC2/4) complex has been extensively studied in Saccharomyces cerevisiae mitosis, but its role in mitosis and meiosis remains poorly understood in multicellular organisms, because complete loss-of-function of either gene causes embryonic lethality. Here, we identified a weak allele of Atscc2 (Atscc2-5) that has only minor defects in vegetative development but exhibits a significant reduction in fertility. Cytological analyses of Atscc2-5 reveal multiple meiotic phenotypes including defects in chromosomal axis formation, meiosis-specific cohesin loading, homolog pairing and synapsis, and AtSPO11-1-dependent double strand break repair. Surprisingly, even though AtSCC2 interacts with AtSCC4 in vitro and in vivo, meiosis-specific knockdown of AtSCC4 expression does not cause any meiotic defect, suggesting that the SCC2-SCC4 complex has divergent roles in mitosis and meiosis. SCC2 homologs from land plants have a unique plant homeodomain (PHD) motif not found in other species. We show that the AtSCC2 PHD domain can bind to the N terminus of histones and is required for meiosis but not mitosis. Taken together, our results provide evidence that unlike SCC2 in other organisms, SCC2 requires a functional PHD domain during meiosis in land plants.
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spelling pubmed-73046472020-06-22 The cohesin loader SCC2 contains a PHD finger that is required for meiosis in land plants Wang, Hongkuan Xu, Wanyue Sun, Yujin Lian, Qichao Wang, Cong Yu, Chaoyi He, Chengpeng Wang, Jun Ma, Hong Copenhaver, Gregory P. Wang, Yingxiang PLoS Genet Research Article Cohesin, a multisubunit protein complex, is required for holding sister chromatids together during mitosis and meiosis. The recruitment of cohesin by the sister chromatid cohesion 2/4 (SCC2/4) complex has been extensively studied in Saccharomyces cerevisiae mitosis, but its role in mitosis and meiosis remains poorly understood in multicellular organisms, because complete loss-of-function of either gene causes embryonic lethality. Here, we identified a weak allele of Atscc2 (Atscc2-5) that has only minor defects in vegetative development but exhibits a significant reduction in fertility. Cytological analyses of Atscc2-5 reveal multiple meiotic phenotypes including defects in chromosomal axis formation, meiosis-specific cohesin loading, homolog pairing and synapsis, and AtSPO11-1-dependent double strand break repair. Surprisingly, even though AtSCC2 interacts with AtSCC4 in vitro and in vivo, meiosis-specific knockdown of AtSCC4 expression does not cause any meiotic defect, suggesting that the SCC2-SCC4 complex has divergent roles in mitosis and meiosis. SCC2 homologs from land plants have a unique plant homeodomain (PHD) motif not found in other species. We show that the AtSCC2 PHD domain can bind to the N terminus of histones and is required for meiosis but not mitosis. Taken together, our results provide evidence that unlike SCC2 in other organisms, SCC2 requires a functional PHD domain during meiosis in land plants. Public Library of Science 2020-06-09 /pmc/articles/PMC7304647/ /pubmed/32516352 http://dx.doi.org/10.1371/journal.pgen.1008849 Text en © 2020 Wang et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Wang, Hongkuan
Xu, Wanyue
Sun, Yujin
Lian, Qichao
Wang, Cong
Yu, Chaoyi
He, Chengpeng
Wang, Jun
Ma, Hong
Copenhaver, Gregory P.
Wang, Yingxiang
The cohesin loader SCC2 contains a PHD finger that is required for meiosis in land plants
title The cohesin loader SCC2 contains a PHD finger that is required for meiosis in land plants
title_full The cohesin loader SCC2 contains a PHD finger that is required for meiosis in land plants
title_fullStr The cohesin loader SCC2 contains a PHD finger that is required for meiosis in land plants
title_full_unstemmed The cohesin loader SCC2 contains a PHD finger that is required for meiosis in land plants
title_short The cohesin loader SCC2 contains a PHD finger that is required for meiosis in land plants
title_sort cohesin loader scc2 contains a phd finger that is required for meiosis in land plants
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7304647/
https://www.ncbi.nlm.nih.gov/pubmed/32516352
http://dx.doi.org/10.1371/journal.pgen.1008849
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