DNALI1 interacts with the MEIG1/PACRG complex within the manchette and is required for proper sperm flagellum assembly in mice

Author:

Yap Yi Tian1ORCID,Li Wei1,Huang Qian12ORCID,Zhou Qi12,Zhang David3,Sheng Yi4,Mladenovic-Lucas Ljljiana5,Yee Siu-Pok6ORCID,Orwig Kyle E4,Granneman James G5ORCID,Williams David C7ORCID,Hess Rex A8ORCID,Toure Aminata9,Zhang Zhibing110ORCID

Affiliation:

1. Department of Physiology, Wayne State University School of Medicine

2. Department of Occupational and Environmental Medicine, School of Public Health, Wuhan University of Science and Technology

3. College of William and Mary

4. Molecular Genetics and Developmental Biology Graduate Program, Department of Obstetrics, Gynecology and Reproductive Sciences, Magee-Womens Research Institute, University of Pittsburgh School of Medicine

5. Center for Molecular Medicine and Genetics, Wayne State University School of Medicine

6. Department of Cell Biology, University of Connecticut Health Center

7. Department of Pathology and Laboratory Medicine, University of North Carolina

8. Department of Comparative Biosciences, College of Veterinary Medicine, University of Illinois

9. University Grenoble Alpes, Inserm U 1209, CNRS UMR 5309, Team Physiology and Pathophysiology of Sperm cells, Institute for Advanced Biosciences

10. Department of Obstetrics & Gynecology, Wayne State University

Abstract

The manchette is a transient and unique structure present in elongating spermatids and required for proper differentiation of the germ cells during spermatogenesis. Previous work indicated that the MEIG1/PACRG complex locates in the manchette and is involved in the transport of cargos, such as SPAG16L, to build the sperm flagellum. Here, using co-immunoprecipitation and pull-down approaches in various cell systems, we established that DNALI1, an axonemal component originally cloned from Chlamydomonas reinhardtii, recruits and stabilizes PACRG and we confirm in vivo, the co-localization of DNALI1 and PACRG in the manchette by immunofluorescence of elongating murine spermatids. We next generated mice with a specific deficiency of DNALI1 in male germ cells, and observed a dramatic reduction of the sperm cells, which results in male infertility. In addition, we observed that the majority of the sperm cells exhibited abnormal morphology including misshapen heads, bent tails, enlarged midpiece, discontinuous accessory structure, emphasizing the importance of DNALI1 in sperm differentiation. Examination of testis histology confirmed impaired spermiogenesis in the mutant mice. Importantly, while testicular levels of MEIG1, PACRG, and SPAG16L proteins were unchanged in the Dnali1 mutant mice, their localization within the manchette was greatly affected, indicating that DNALI1 is required for the formation of the MEIG1/PACRG complex within the manchette. Interestingly, in contrast to MEIG1 and PACRG-deficient mice, the DNALI1-deficient mice also showed impaired sperm spermiation/individualization, suggesting additional functions beyond its involvement in the manchette structure. Overall, our work identifies DNALI1 as a protein required for sperm development.

Funder

Wayne State University Startup fund

Wayne State University Research Fund

Male Contraceptive Initiative fellowship

Male Contraceptive Initiative pilot award

National Institute of Child Health and Human Development

National Institute of Diabetes and Digestive and Kidney Diseases

Agence Nationale pour la Recherche

Publisher

eLife Sciences Publications, Ltd

Subject

General Immunology and Microbiology,General Biochemistry, Genetics and Molecular Biology,General Medicine,General Neuroscience

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