PIWI proteins are essential for early Drosophila embryogenesis

PIWI proteins, a subfamily of the ARGONAUTE/PIWI protein family, have been implicated in transcriptional and posttranscriptional gene regulation and transposon silencing mediated by small non-coding RNAs, especially piRNAs. Although these proteins are known to be required for germline development, t...

Full description

Saved in:
Bibliographic Details
Published inDevelopmental biology Vol. 385; no. 2; pp. 340 - 349
Main Authors Mani, Sneha Ramesh, Megosh, Heather, Lin, Haifan
Format Journal Article
LanguageEnglish
Published United States Elsevier Inc 15.01.2014
Subjects
Online AccessGet full text

Cover

Loading…
More Information
Summary:PIWI proteins, a subfamily of the ARGONAUTE/PIWI protein family, have been implicated in transcriptional and posttranscriptional gene regulation and transposon silencing mediated by small non-coding RNAs, especially piRNAs. Although these proteins are known to be required for germline development, their somatic function remains elusive. Here, we examine the maternal function of all three PIWI proteins in Drosophila; Piwi, Aubergine (Aub) and Argonaute3 (Ago3) during early embryogenesis. In syncytial embryos, Piwi displays an embryonic stage-dependent localization pattern. Piwi is localized in the cytoplasm during mitotic cycles 1–10. Between cycles 11 and 14, Piwi remains in the cytoplasm during mitosis but moves into the somatic nucleus during interphase. Beyond cycle 14, it stays in the nucleus. Aub and Ago3 are diffusely cytoplasmic from cycle 1 to 14. Embryos maternally depleted of any one of the three PIWI proteins display severe mitotic defects, including abnormal chromosome and nuclear morphology, cell cycle arrest, asynchronous nuclear division and aberrant nuclear migration. Furthermore, all three PIWI proteins are required for the assembly of mitotic machinery and progression through mitosis. Embryos depleted of maternal PIWI proteins also exhibit chromatin organization abnormalities. These observations indicate that maternal Piwi, Aub and Ago3 play a critical role in the maintenance of chromatin structure and cell cycle progression during early embryogenesis, with compromised chromatin integrity as a possible cause of the observed mitotic defects. Our study demonstrates the essential function of PIWI proteins in the first phase of somatic development. •Drosophila embryos contain all three PIWI proteins as maternal factors.•Embryos depleted of a maternal PIWI proteins display severe mitotic defects.•Embryos depleted of a maternal PIWI protein exhibit chromatin abnormalities.•PIWI proteins are essential for the first phase of somatic development.
Bibliography:Co-First Authors
Current Affiliation: McKinsey and Company, 2929 Arch Street, Philadelphia, PA
ISSN:0012-1606
1095-564X
DOI:10.1016/j.ydbio.2013.10.017