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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...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Life Science Alliance LLC
2021
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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. |
format | Online Article Text |
id | pubmed-8200288 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Life Science Alliance LLC |
record_format | MEDLINE/PubMed |
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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