دورية أكاديمية
Large-scale analyses of the X chromosome in 2,354 infertile men discover recurrently affected genes associated with spermatogenic failure.
| العنوان: | Large-scale analyses of the X chromosome in 2,354 infertile men discover recurrently affected genes associated with spermatogenic failure. |
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| المؤلفون: | Riera-Escamilla A; Andrology Department, Fundació Puigvert, Universitat Autònoma de Barcelona, Instituto de Investigaciones Biomédicas Sant Pau, Barcelona, 08025 Catalonia, Spain., Vockel M; Institute of Human Genetics, University of Münster, Vesaliusweg 12-14, 48149 Münster, Germany., Nagirnaja L; Division of Genetics, Oregon National Primate Research Center, Oregon Health & Science University, Beaverton, OR 97006, USA., Xavier MJ; Faculty of Medical Sciences, Biosciences Institute, Newcastle University, Newcastle upon Tyne NE2 4HH, UK., Carbonell A; Institute of Molecular Biology of Barcelona, CSIC, Baldiri Reixac, 4, Barcelona, 08028 Catalonia, Spain; Institute for Research in Biomedicine, IRB Barcelona, The Barcelona Institute for Science and Technology, Baldiri Reixac, 10, Barcelona, 08028 Catalonia, Spain., Moreno-Mendoza D; Andrology Department, Fundació Puigvert, Universitat Autònoma de Barcelona, Instituto de Investigaciones Biomédicas Sant Pau, Barcelona, 08025 Catalonia, Spain; Department of Urology, Hospital del Oriente de Asturias, Arriondas, 33540 Asturias, Spain., Pybus M; Molecular Biology Laboratory, Fundació Puigvert, Instituto de Investigaciones Biomédicas Sant Pau, Universitat Autònoma de Barcelona, Barcelona, 08025 Catalonia, Spain., Farnetani G; Department of Biomedical, Experimental and Clinical Sciences Mario Serio, University of Florence, Florence 50139, Italy., Rosta V; Department of Biomedical, Experimental and Clinical Sciences Mario Serio, University of Florence, Florence 50139, Italy., Cioppi F; Department of Biomedical, Experimental and Clinical Sciences Mario Serio, University of Florence, Florence 50139, Italy., Friedrich C; Institute of Reproductive Genetics, University of Münster, Vesaliusweg 12-14, 48149 Münster, Germany., Oud MS; Department of Human Genetics, Donders Institute for Brain, Cognition and Behaviour, Radboudumc, Nijmegen 6525, the Netherlands., van der Heijden GW; Department of Obstetrics and Gynaecology, Radboudumc, Nijmegen 6525, the Netherlands., Soave A; Department of Urology, University Medical Center Hamburg-Eppendorf, Hamburg 20251, Germany., Diemer T; Clinic for Urology, Paediatric Urology and Andrology, Justus Liebig University, Gießen 35392, Germany., Ars E; Molecular Biology Laboratory, Fundació Puigvert, Instituto de Investigaciones Biomédicas Sant Pau, Universitat Autònoma de Barcelona, Barcelona, 08025 Catalonia, Spain., Sánchez-Curbelo J; Andrology Department, Fundació Puigvert, Universitat Autònoma de Barcelona, Instituto de Investigaciones Biomédicas Sant Pau, Barcelona, 08025 Catalonia, Spain., Kliesch S; Centre of Reproductive Medicine and Andrology, Department of Clinical and Surgical Andrology, University Hospital Münster, Münster 48149, Germany., O'Bryan MK; The School of BioScience that the Bio21 Institute, The Faculty of Science, The University of Melbourne, Melbourne, VIC 3010, Australia., Ruiz-Castañe E; Andrology Department, Fundació Puigvert, Universitat Autònoma de Barcelona, Instituto de Investigaciones Biomédicas Sant Pau, Barcelona, 08025 Catalonia, Spain., Azorín F; Institute of Molecular Biology of Barcelona, CSIC, Baldiri Reixac, 4, Barcelona, 08028 Catalonia, Spain; Institute for Research in Biomedicine, IRB Barcelona, The Barcelona Institute for Science and Technology, Baldiri Reixac, 10, Barcelona, 08028 Catalonia, Spain., Veltman JA; Faculty of Medical Sciences, Biosciences Institute, Newcastle University, Newcastle upon Tyne NE2 4HH, UK., Aston KI; Andrology and IVF Laboratories, Division of Urology, Department of Surgery, University of Utah School of Medicine, Salt Lake City, UT 84132, USA., Conrad DF; Division of Genetics, Oregon National Primate Research Center, Oregon Health & Science University, Beaverton, OR 97006, USA; Department of Genetics, Washington University School of Medicine, St. Louis, MO 63110, USA., Tüttelmann F; Institute of Reproductive Genetics, University of Münster, Vesaliusweg 12-14, 48149 Münster, Germany., Krausz C; Department of Biomedical, Experimental and Clinical Sciences Mario Serio, University of Florence, Florence 50139, Italy. Electronic address: csilla.krausz@unifi.it. |
| مؤلفون مشاركون: | GEMINI Consortium |
| المصدر: | American journal of human genetics [Am J Hum Genet] 2022 Aug 04; Vol. 109 (8), pp. 1458-1471. Date of Electronic Publication: 2022 Jul 08. |
| نوع المنشور: | Journal Article; Research Support, N.I.H., Extramural; Research Support, Non-U.S. Gov't |
| اللغة: | English |
| بيانات الدورية: | Publisher: Cell Press Country of Publication: United States NLM ID: 0370475 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1537-6605 (Electronic) Linking ISSN: 00029297 NLM ISO Abbreviation: Am J Hum Genet Subsets: MEDLINE |
| أسماء مطبوعة: | Publication: 2008- : [Cambridge, MA] : Cell Press Original Publication: Baltimore, American Society of Human Genetics. |
| مواضيع طبية MeSH: | Azoospermia*/genetics , Infertility, Male*/genetics , Oligospermia*, Humans ; Male ; Spermatogenesis/genetics ; X Chromosome |
| مستخلص: | Although the evolutionary history of the X chromosome indicates its specialization in male fitness, its role in spermatogenesis has largely been unexplored. Currently only three X chromosome genes are considered of moderate-definitive diagnostic value. We aimed to provide a comprehensive analysis of all X chromosome-linked protein-coding genes in 2,354 azoospermic/cryptozoospermic men from four independent cohorts. Genomic data were analyzed and compared with data in normozoospermic control individuals and gnomAD. While updating the clinical significance of known genes, we propose 21 recurrently mutated genes strongly associated with and 34 moderately associated with azoospermia/cryptozoospermia not previously linked to male infertility (novel). The most frequently affected prioritized gene, RBBP7, was found mutated in ten men across all cohorts, and our functional studies in Drosophila support its role in germ stem cell maintenance. Collectively, our study represents a significant step towards the definition of the missing genetic etiology in idiopathic severe spermatogenic failure and significantly reduces the knowledge gap of X-linked genetic causes of azoospermia/cryptozoospermia contributing to the development of future diagnostic gene panels. Competing Interests: Declaration of interests The authors declare no competing interests. (Copyright © 2022. Published by Elsevier Inc.) |
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| معلومات مُعتمدة: | United Kingdom WT_ Wellcome Trust; 209451/Z/17/Z United Kingdom WT_ Wellcome Trust; R01 HD078641 United States HD NICHD NIH HHS; 209451 United Kingdom WT_ Wellcome Trust |
| فهرسة مساهمة: | Keywords: RBBP7; X chromosome; azoospermia; cryptozoospermia; genes; genetics; genomics; male infertility; next-generation sequencing; spermatogenesis |
| تواريخ الأحداث: | Date Created: 20220709 Date Completed: 20220809 Latest Revision: 20230205 |
| رمز التحديث: | 20230205 |
| مُعرف محوري في PubMed: | PMC9388793 |
| DOI: | 10.1016/j.ajhg.2022.06.007 |
| PMID: | 35809576 |
| قاعدة البيانات: | MEDLINE |
| تدمد: | 1537-6605 |
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| DOI: | 10.1016/j.ajhg.2022.06.007 |