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Transcriptome analyses in infertile men reveal germ cell–specific expression and splicing patterns
The process of spermatogenesis—when germ cells differentiate into sperm—is tightly regulated, and misregulation in gene expression is likely to be involved in the physiopathology of male infertility. The testis is one of the most transcriptionally rich tissues; nevertheless, the specific gene expres...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Life Science Alliance LLC
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9713473/ https://www.ncbi.nlm.nih.gov/pubmed/36446526 http://dx.doi.org/10.26508/lsa.202201633 |
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author | Siebert-Kuss, Lara M Krenz, Henrike Tekath, Tobias Wöste, Marius Di Persio, Sara Terwort, Nicole Wyrwoll, Margot J Cremers, Jann-Frederik Wistuba, Joachim Dugas, Martin Kliesch, Sabine Schlatt, Stefan Tüttelmann, Frank Gromoll, Jörg Neuhaus, Nina Laurentino, Sandra |
author_facet | Siebert-Kuss, Lara M Krenz, Henrike Tekath, Tobias Wöste, Marius Di Persio, Sara Terwort, Nicole Wyrwoll, Margot J Cremers, Jann-Frederik Wistuba, Joachim Dugas, Martin Kliesch, Sabine Schlatt, Stefan Tüttelmann, Frank Gromoll, Jörg Neuhaus, Nina Laurentino, Sandra |
author_sort | Siebert-Kuss, Lara M |
collection | PubMed |
description | The process of spermatogenesis—when germ cells differentiate into sperm—is tightly regulated, and misregulation in gene expression is likely to be involved in the physiopathology of male infertility. The testis is one of the most transcriptionally rich tissues; nevertheless, the specific gene expression changes occurring during spermatogenesis are not fully understood. To better understand gene expression during spermatogenesis, we generated germ cell–specific whole transcriptome profiles by systematically comparing testicular transcriptomes from tissues in which spermatogenesis is arrested at successive steps of germ cell differentiation. In these comparisons, we found thousands of differentially expressed genes between successive germ cell types of infertility patients. We demonstrate our analyses’ potential to identify novel highly germ cell–specific markers (TSPY4 and LUZP4 for spermatogonia; HMGB4 for round spermatids) and identified putatively misregulated genes in male infertility (RWDD2A, CCDC183, CNNM1, SERF1B). Apart from these, we found thousands of genes showing germ cell–specific isoforms (including SOX15, SPATA4, SYCP3, MKI67). Our approach and dataset can help elucidate genetic and transcriptional causes for male infertility. |
format | Online Article Text |
id | pubmed-9713473 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Life Science Alliance LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-97134732022-12-02 Transcriptome analyses in infertile men reveal germ cell–specific expression and splicing patterns Siebert-Kuss, Lara M Krenz, Henrike Tekath, Tobias Wöste, Marius Di Persio, Sara Terwort, Nicole Wyrwoll, Margot J Cremers, Jann-Frederik Wistuba, Joachim Dugas, Martin Kliesch, Sabine Schlatt, Stefan Tüttelmann, Frank Gromoll, Jörg Neuhaus, Nina Laurentino, Sandra Life Sci Alliance Resources The process of spermatogenesis—when germ cells differentiate into sperm—is tightly regulated, and misregulation in gene expression is likely to be involved in the physiopathology of male infertility. The testis is one of the most transcriptionally rich tissues; nevertheless, the specific gene expression changes occurring during spermatogenesis are not fully understood. To better understand gene expression during spermatogenesis, we generated germ cell–specific whole transcriptome profiles by systematically comparing testicular transcriptomes from tissues in which spermatogenesis is arrested at successive steps of germ cell differentiation. In these comparisons, we found thousands of differentially expressed genes between successive germ cell types of infertility patients. We demonstrate our analyses’ potential to identify novel highly germ cell–specific markers (TSPY4 and LUZP4 for spermatogonia; HMGB4 for round spermatids) and identified putatively misregulated genes in male infertility (RWDD2A, CCDC183, CNNM1, SERF1B). Apart from these, we found thousands of genes showing germ cell–specific isoforms (including SOX15, SPATA4, SYCP3, MKI67). Our approach and dataset can help elucidate genetic and transcriptional causes for male infertility. Life Science Alliance LLC 2022-11-29 /pmc/articles/PMC9713473/ /pubmed/36446526 http://dx.doi.org/10.26508/lsa.202201633 Text en © 2022 Siebert-Kuss 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 | Resources Siebert-Kuss, Lara M Krenz, Henrike Tekath, Tobias Wöste, Marius Di Persio, Sara Terwort, Nicole Wyrwoll, Margot J Cremers, Jann-Frederik Wistuba, Joachim Dugas, Martin Kliesch, Sabine Schlatt, Stefan Tüttelmann, Frank Gromoll, Jörg Neuhaus, Nina Laurentino, Sandra Transcriptome analyses in infertile men reveal germ cell–specific expression and splicing patterns |
title | Transcriptome analyses in infertile men reveal germ cell–specific expression and splicing patterns |
title_full | Transcriptome analyses in infertile men reveal germ cell–specific expression and splicing patterns |
title_fullStr | Transcriptome analyses in infertile men reveal germ cell–specific expression and splicing patterns |
title_full_unstemmed | Transcriptome analyses in infertile men reveal germ cell–specific expression and splicing patterns |
title_short | Transcriptome analyses in infertile men reveal germ cell–specific expression and splicing patterns |
title_sort | transcriptome analyses in infertile men reveal germ cell–specific expression and splicing patterns |
topic | Resources |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9713473/ https://www.ncbi.nlm.nih.gov/pubmed/36446526 http://dx.doi.org/10.26508/lsa.202201633 |
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