Alstrom syndrome gene is a stem-cell-specific regulator of centriole duplication in the Drosophila testis

Author:

Chen Cuie1ORCID,Yamashita Yukiko M1234ORCID

Affiliation:

1. Life Science Institute, Department of Cell and Developmental Biology, Michigan Medicine, University of Michigan, Ann Arbor, United States

2. Howard Hughes Medical Institute, Cambridge, United States

3. Whitehead Institute for Biomedical Research, Cambridge, United States

4. Department of Biology, Massachusetts Institute of Technology, Cambridge, United States

Abstract

Asymmetrically dividing stem cells often show asymmetric behavior of the mother versus daughter centrosomes, whereby the self-renewing stem cell selectively inherits the mother or daughter centrosome. Although the asymmetric centrosome behavior is widely conserved, its biological significance remains largely unclear. Here, we show that Alms1a, a Drosophila homolog of the human ciliopathy gene Alstrom syndrome, is enriched on the mother centrosome in Drosophila male germline stem cells (GSCs). Depletion of alms1a in GSCs, but not in differentiating germ cells, results in rapid loss of centrosomes due to a failure in daughter centriole duplication, suggesting that Alms1a has a stem-cell-specific function in centrosome duplication. Alms1a interacts with Sak/Plk4, a critical regulator of centriole duplication, more strongly at the GSC mother centrosome, further supporting Alms1a’s unique role in GSCs. Our results begin to reveal the unique regulation of stem cell centrosomes that may contribute to asymmetric stem cell divisions.

Funder

Howard Hughes Medical Institute

National Institute of General Medical Sciences

Publisher

eLife Sciences Publications, Ltd

Subject

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

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