{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,6,13]],"date-time":"2026-06-13T17:57:30Z","timestamp":1781373450469,"version":"3.54.1"},"reference-count":46,"publisher":"Oxford University Press (OUP)","issue":"7","license":[{"start":{"date-parts":[[2024,5,13]],"date-time":"2024-05-13T00:00:00Z","timestamp":1715558400000},"content-version":"vor","delay-in-days":0,"URL":"https:\/\/academic.oup.com\/pages\/standard-publication-reuse-rights"}],"funder":[{"DOI":"10.13039\/501100001412","name":"Council of Scientific and Industrial Research","doi-asserted-by":"crossref","id":[{"id":"10.13039\/501100001412","id-type":"DOI","asserted-by":"crossref"}]}],"content-domain":{"domain":[],"crossmark-restriction":false},"short-container-title":[],"published-print":{"date-parts":[[2024,7,1]]},"abstract":"Abstract<\/jats:title>\n \n STUDY QUESTION<\/jats:title>\n What is the functional significance of Tex13b in male germ cell development and differentiation?<\/jats:p>\n <\/jats:sec>\n \n SUMMARY ANSWER<\/jats:title>\n Tex13b regulates male germ cell differentiation by metabolic reprogramming during spermatogenesis.<\/jats:p>\n <\/jats:sec>\n \n WHAT IS KNOWN ALREADY<\/jats:title>\n Studies in mice and humans suggest that TEX13B is a transcription factor and is exclusively expressed in germ cells.<\/jats:p>\n <\/jats:sec>\n \n STUDY DESIGN, SIZE, DURATION<\/jats:title>\n We sequenced the coding regions of TEX13B in 628 infertile men and 427 ethnically matched fertile control men. Further, to identify the molecular function of Tex13b, we created a Tex13b knockout and conditional overexpression system in GC-1spg (hereafter, GC-1) cells.<\/jats:p>\n <\/jats:sec>\n \n PARTICIPANTS\/MATERIALS, SETTING, METHODS<\/jats:title>\n Our recent exome sequencing study identified novel candidate genes for male infertility. TEX13B was found to be one of the potential candidates, hence we explored the role of TEX13B in male infertility within a large infertile case\u2013control cohort. We performed functional analyses of Tex13b in a GC-1 cell line using CRISPR-Cas9. We differentially labelled the cell proteins by stable isotope labelling of amino acids in cell culture (SILAC) and performed mass spectrometry-based whole-cell proteomics to identify the differential protein regulation in knockout cells compared to wild-type cells. We found that Tex13b knockout leads to downregulation of the OXPHOS complexes and upregulation of glycolysis genes, which was further validated by western blotting. These results were further confirmed by respirometry analysis in Tex13b knockout cells. Further, we also performed a conditional overexpression of TEX13B in GC-1 cells and studied the expression of OXPHOS complex proteins by western blotting.<\/jats:p>\n <\/jats:sec>\n \n MAIN RESULTS AND THE ROLE OF CHANCE<\/jats:title>\n We identified a rare variant, rs775429506 (p.Gly237Glu), exclusively in two non-obstructive-azoospermia (NOA) men, that may genetically predispose these men for infertility. Further, we demonstrated that Tex13b functions in the transcription regulation of OXPHOS complexes.<\/jats:p>\n <\/jats:sec>\n \n LARGE SCALE DATA<\/jats:title>\n N\/A.<\/jats:p>\n <\/jats:sec>\n \n LIMITATIONS, REASONS FOR CAUTION<\/jats:title>\n We examined the function of Tex13b in GC-1 in vitro by knocking out and conditional overexpression, for understanding the function of Tex13b in germ cells. Unfortunately, this could not be replicated in either an animal model or in patient-derived tissue due to the non-availability of an animal model or patient\u2019s testis biopsies.<\/jats:p>\n <\/jats:sec>\n \n WIDER IMPLICATIONS OF THE FINDINGS<\/jats:title>\n This study identified that Tex13b plays an important role in male germ cell development and differentiation. The findings of this study would be useful for screening infertile males with spermatogenic failure and counselling them before the implementation of assisted reproduction technique(s).<\/jats:p>\n <\/jats:sec>\n \n STUDY FUNDING\/COMPETING INTEREST(S)<\/jats:title>\n Funding was provided by the Council of Scientific and Industrial Research (CSIR) under the network project (BSC0101 and MLP0113) and SERB, the Department of Science and Technology, Government of India (J C Bose Fellowship: JCB\/2019\/000027). The authors do not have any competing interest.<\/jats:p>\n <\/jats:sec>","DOI":"10.1093\/humrep\/deae094","type":"journal-article","created":{"date-parts":[[2024,5,14]],"date-time":"2024-05-14T03:53:38Z","timestamp":1715658818000},"page":"1390-1403","source":"Crossref","is-referenced-by-count":4,"title":["TEX13B<\/i> is essential for metabolic reprogramming during germ cell differentiation"],"prefix":"10.1093","volume":"39","author":[{"given":"Umesh","family":"Kumar","sequence":"first","affiliation":[{"name":"CSIR-Centre for Cellular and Molecular Biology (CCMB) , Hyderabad, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-3373-8592","authenticated-orcid":false,"given":"Digumarthi V S","family":"Sudhakar","sequence":"additional","affiliation":[{"name":"CSIR-Centre for Cellular and Molecular Biology (CCMB) , Hyderabad, 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Deenadayal","family":"Tolani","sequence":"additional","affiliation":[{"name":"Infertility Institute and Research Center (IIRC), Mamata Fertility Hospital , Hyderabad, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Swasti","family":"Raychaudhuri","sequence":"additional","affiliation":[{"name":"CSIR-Centre for Cellular and Molecular Biology (CCMB) , Hyderabad, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"P","family":"Chandra Shekar","sequence":"additional","affiliation":[{"name":"CSIR-Centre for Cellular and Molecular Biology (CCMB) , Hyderabad, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-0075-0106","authenticated-orcid":false,"given":"Kumarasamy","family":"Thangaraj","sequence":"additional","affiliation":[{"name":"CSIR-Centre for Cellular and Molecular Biology (CCMB) , Hyderabad, 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