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Gametic specialization of centromeric histone paralogs in Drosophila virilis

In most eukaryotes, centromeric histone (CenH3) proteins mediate mitosis and meiosis and ensure epigenetic inheritance of centromere identity. We hypothesized that disparate chromatin environments in soma versus germline might impose divergent functional requirements on single CenH3 genes, which cou...

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Autores principales: Kursel, Lisa E, McConnell, Hannah, de la Cruz, Aida Flor A, Malik, Harmit S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Life Science Alliance LLC 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8200288/
https://www.ncbi.nlm.nih.gov/pubmed/33986021
http://dx.doi.org/10.26508/lsa.202000992
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author Kursel, Lisa E
McConnell, Hannah
de la Cruz, Aida Flor A
Malik, Harmit S
author_facet Kursel, Lisa E
McConnell, Hannah
de la Cruz, Aida Flor A
Malik, Harmit S
author_sort Kursel, Lisa E
collection PubMed
description In most eukaryotes, centromeric histone (CenH3) proteins mediate mitosis and meiosis and ensure epigenetic inheritance of centromere identity. We hypothesized that disparate chromatin environments in soma versus germline might impose divergent functional requirements on single CenH3 genes, which could be ameliorated by gene duplications and subsequent specialization. Here, we analyzed the cytological localization of two recently identified CenH3 paralogs, Cid1 and Cid5, in Drosophila virilis using specific antibodies and epitope-tagged transgenic strains. We find that only ancestral Cid1 is present in somatic cells, whereas both Cid1 and Cid5 are expressed in testes and ovaries. However, Cid1 is lost in male meiosis but retained throughout oogenesis, whereas Cid5 is lost during female meiosis but retained in mature sperm. Following fertilization, only Cid1 is detectable in the early embryo, suggesting that maternally deposited Cid1 is rapidly loaded onto paternal centromeres during the protamine-to-histone transition. Our studies reveal mutually exclusive gametic specialization of divergent CenH3 paralogs. Duplication and divergence might allow essential centromeric genes to resolve an intralocus conflict between maternal and paternal centromeric requirements in many animal species.
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spelling pubmed-82002882021-06-24 Gametic specialization of centromeric histone paralogs in Drosophila virilis Kursel, Lisa E McConnell, Hannah de la Cruz, Aida Flor A Malik, Harmit S Life Sci Alliance Research Articles In most eukaryotes, centromeric histone (CenH3) proteins mediate mitosis and meiosis and ensure epigenetic inheritance of centromere identity. We hypothesized that disparate chromatin environments in soma versus germline might impose divergent functional requirements on single CenH3 genes, which could be ameliorated by gene duplications and subsequent specialization. Here, we analyzed the cytological localization of two recently identified CenH3 paralogs, Cid1 and Cid5, in Drosophila virilis using specific antibodies and epitope-tagged transgenic strains. We find that only ancestral Cid1 is present in somatic cells, whereas both Cid1 and Cid5 are expressed in testes and ovaries. However, Cid1 is lost in male meiosis but retained throughout oogenesis, whereas Cid5 is lost during female meiosis but retained in mature sperm. Following fertilization, only Cid1 is detectable in the early embryo, suggesting that maternally deposited Cid1 is rapidly loaded onto paternal centromeres during the protamine-to-histone transition. Our studies reveal mutually exclusive gametic specialization of divergent CenH3 paralogs. Duplication and divergence might allow essential centromeric genes to resolve an intralocus conflict between maternal and paternal centromeric requirements in many animal species. Life Science Alliance LLC 2021-05-13 /pmc/articles/PMC8200288/ /pubmed/33986021 http://dx.doi.org/10.26508/lsa.202000992 Text en © 2021 Kursel et al. https://creativecommons.org/licenses/by/4.0/This article is available under a Creative Commons License (Attribution 4.0 International, as described at https://creativecommons.org/licenses/by/4.0/).
spellingShingle Research Articles
Kursel, Lisa E
McConnell, Hannah
de la Cruz, Aida Flor A
Malik, Harmit S
Gametic specialization of centromeric histone paralogs in Drosophila virilis
title Gametic specialization of centromeric histone paralogs in Drosophila virilis
title_full Gametic specialization of centromeric histone paralogs in Drosophila virilis
title_fullStr Gametic specialization of centromeric histone paralogs in Drosophila virilis
title_full_unstemmed Gametic specialization of centromeric histone paralogs in Drosophila virilis
title_short Gametic specialization of centromeric histone paralogs in Drosophila virilis
title_sort gametic specialization of centromeric histone paralogs in drosophila virilis
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8200288/
https://www.ncbi.nlm.nih.gov/pubmed/33986021
http://dx.doi.org/10.26508/lsa.202000992
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