Gametic specialization of centromeric histone paralogs in Drosophila virilis

Author:

Kursel Lisa E12,McConnell Hannah2,de la Cruz Aida Flor A23,Malik Harmit S23ORCID

Affiliation:

1. Molecular and Cellular Biology Graduate Program, University of Washington, Seattle, WA, USA

2. Division of Basic Sciences, Fred Hutchinson Cancer Research Center, Seattle, WA, USA

3. Howard Hughes Medical Institute, Fred Hutchinson Cancer Research Center, Seattle, WA, USA

Abstract

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.

Funder

National Institutes of Health training grants

National Institutes of Health grant

Publisher

Life Science Alliance, LLC

Subject

Health, Toxicology and Mutagenesis,Plant Science,Biochemistry, Genetics and Molecular Biology (miscellaneous),Ecology

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