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dc.contributor.authorOlotu, Opeyemi
dc.contributor.authorDowling, Mark
dc.contributor.authorHomolka, David
dc.contributor.authorWojtas, Magdalena Natalia
dc.contributor.authorTran, Panyi
dc.contributor.authorLehtiniemi, Tiina
dc.contributor.authorDa Ros, Matteo
dc.contributor.authorPillai, Ramesh S.
dc.contributor.authorKotaja, Noora
dc.date.accessioned2023-05-09T14:43:01Z
dc.date.available2023-05-09T14:43:01Z
dc.date.issued2023-05
dc.identifier.citationAndrology 11(4) : 710-723 (2023)es_ES
dc.identifier.issn2047-2919
dc.identifier.issn2047-2927
dc.identifier.urihttp://hdl.handle.net/10810/61059
dc.description.abstractBackground Germ granules are large cytoplasmic ribonucleoprotein complexes that emerge in the germline to participate in RNA regulation. The two most prominent germ granules are the intermitochondrial cement (IMC) in meiotic spermatocytes and the chromatoid body (CB) in haploid round spermatids, both functionally linked to the PIWI-interacting RNA (piRNA) pathway. Aims In this study, we clarified the IMC function by identifying proteins that form complexes with a well-known IMC protein PIWIL2/MILI in the mouse testis. Results The PIWIL2 interactome included several proteins with known functions in piRNA biogenesis. We further characterized the expression and localization of two of the identified proteins, Exonuclease 3′–5′ domain-containing proteins EXD1 and EXD2, and confirmed their localization to the IMC. We showed that EXD2 interacts with PIWIL2, and that the mutation of Exd2 exonuclease domain in mice induces misregulation of piRNA levels originating from specific pachytene piRNA clusters, but does not disrupt male fertility. Conclusion Altogether, this study highlights the central role of the IMC as a platform for piRNA biogenesis, and suggests that EXD1 and EXD2 function in the IMC-mediated RNA regulation in postnatal male germ cells.es_ES
dc.description.sponsorshipWe would like to thank all Kotaja lab members for their support and help. The Turku BioScience Cell Imaging and Proteomics Core Facilities are acknowledged for their services and Turku Center for Disease Modeling (TCDM) and Turku Central Animal Facility for providing expertise on animal experimentation. This study was supported by the Academy of Finland, the Sigrid Jusélius Foundation, the Novo Nordisk Foundation, the Jalmari and Rauha Ahokas Foundation, Turku Doctoral Programme of Molecular Medicine (TuDMM), and the Finnish Cultural Foundation.es_ES
dc.language.isoenges_ES
dc.publisherWileyes_ES
dc.rightsinfo:eu-repo/semantics/openAccesses_ES
dc.rights.urihttp://creativecommons.org/licenses/by/3.0/es/*
dc.subjectchromatoid bodyes_ES
dc.subjectEXD1es_ES
dc.subjectEXD2es_ES
dc.subjectintermitochondrial cementes_ES
dc.subjectpiRNAes_ES
dc.subjectspermatogenesises_ES
dc.titleIntermitochondrial cement (IMC) harbors piRNA biogenesis machinery and exonuclease domain-containing proteins EXD1 and EXD2 in mouse spermatocyteses_ES
dc.typeinfo:eu-repo/semantics/articlees_ES
dc.rights.holder© 2023 The Authors. Andrology published by Wiley Periodicals LLC on behalf of American Society of Andrology and European Academy of Andrology. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.es_ES
dc.rights.holderAtribución 3.0 España*
dc.relation.publisherversionhttps://onlinelibrary.wiley.com/doi/10.1111/andr.13361es_ES
dc.identifier.doi10.1111/andr.13361
dc.departamentoesBiología celular e histologíaes_ES
dc.departamentoeuZelulen biologia eta histologiaes_ES


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© 2023 The Authors. Andrology published by Wiley Periodicals LLC on behalf of American Society of Andrology and European Academy of Andrology.

This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
Except where otherwise noted, this item's license is described as © 2023 The Authors. Andrology published by Wiley Periodicals LLC on behalf of American Society of Andrology and European Academy of Andrology. This is an open access article under the terms of the Creative Commons Attribution License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.