Abstract

The conserved RNA helicase Vasa is required for germ cell development in many organisms. In Drosophila melanogaster loss of PIWI-interacting RNA pathway components, including Vasa, causes Chk2-dependent oogenesis arrest. However, whether the arrest is due to Chk2 signaling at a specific stage and whether continuous Chk2 signaling is required for the arrest is unknown. Here, we show that absence of Vasa during the germarial stages causes Chk2-dependent oogenesis arrest. Additionally, we report the age-dependent decline of the ovariole number both in flies lacking Vasa expression only in the germarium and in loss-of-function vasa mutant flies. We show that Chk2 activation exclusively in the germarium is sufficient to interrupt oogenesis and to reduce ovariole number in aging flies. Once induced in the germarium, Chk2-mediated arrest of germ cell development cannot be overcome by restoration of Vasa or by downregulation of Chk2 in the arrested egg chambers. These findings, together with the identity of Vasa-associated proteins identified in this study, demonstrate an essential role of the helicase in the germ cell lineage maintenance and indicate a function of Vasa in germline stem cell homeostasis.

Highlights

  • The conserved RNA helicase Vasa is required for germ cell development in many organisms

  • Our study reveals that sole exclusion of Vas from the germarium causes checkpoint kinase 2 (Chk2)-dependent arrest of oogenesis and a reduction of ovariole number in aging flies

  • These results suggest that the helicase activity of Vas is required for oogenesis and embryogenesis

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Summary

Introduction

The conserved RNA helicase Vasa is required for germ cell development in many organisms. Once induced in the germarium, Chk2-mediated arrest of germ cell development cannot be overcome by restoration of Vasa or by downregulation of Chk in the arrested egg chambers. These findings, together with the identity of Vasaassociated proteins identified in this study, demonstrate an essential role of the helicase in the germ cell lineage maintenance and indicate a function of Vasa in germline stem cell homeostasis. Our study reveals that sole exclusion of Vas from the germarium causes Chk2-dependent arrest of oogenesis and a reduction of ovariole number in aging flies. Activity of Vas RNA helicase early in oogenesis is essential to prevent activation of Chk signaling and license the germline component of the Drosophila ovary for further development

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