Alstrom syndrome gene is a stem-cell-specific regulator of centriole duplication in the <i>Drosophila</i> testis.

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 <i>Drosophila</i> homolog of the human ciliopathy gene Alstrom syndrome, is enriched on the mother centrosome in <i>Drosophila</i> male germline stem cells (GSCs). Depletion of <i>alms1a</i> 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.