Transcriptome analyses in infertile men reveal germ cell–specific expression and splicing patterns

Author:

Siebert-Kuss Lara M1ORCID,Krenz Henrike2,Tekath Tobias2ORCID,Wöste Marius2,Di Persio Sara1ORCID,Terwort Nicole1,Wyrwoll Margot J3,Cremers Jann-Frederik4,Wistuba Joachim1ORCID,Dugas Martin25ORCID,Kliesch Sabine4,Schlatt Stefan1,Tüttelmann Frank3ORCID,Gromoll Jörg1,Neuhaus Nina1ORCID,Laurentino Sandra1ORCID

Affiliation:

1. Centre of Reproductive Medicine and Andrology, Institute of Reproductive and Regenerative Biology, University of Münster, Münster, Germany

2. Institute of Medical Informatics, University of Münster, Münster, Germany

3. Institute of Reproductive Genetics, University of Münster, Münster, Germany

4. Department of Clinical and Surgical Andrology, Centre of Reproductive Medicine and Andrology, University Hospital of Münster, Münster, Germany

5. Institute of Medical Informatics, Heidelberg University Hospital, Heidelberg, Germany

Abstract

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 (includingSOX15,SPATA4,SYCP3,MKI67). Our approach and dataset can help elucidate genetic and transcriptional causes for male infertility.

Funder

German Research Foundation

CeRA

Open Access Publication Fund of the University of Münster

Publisher

Life Science Alliance, LLC

Subject

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

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