A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Reference Report

Reference
Citation Olivieri, D., Senti, K.A., Subramanian, S., Sachidanandam, R., Brennecke, J. (2012). The Cochaperone Shutdown Defines a Group of Biogenesis Factors Essential for All piRNA Populations in Drosophila.  Mol. Cell 47(6): 954--969. (Export to RIS)
FlyBase ID FBrf0219572
Publication Type Research paper
PubMed ID 22902557
PubMed Abstract In animal gonads, PIWI proteins and their bound 23-30 nt piRNAs guard genome integrity by the sequence specific silencing of transposons. Two branches of piRNA biogenesis, namely primary processing and ping-pong amplification, have been proposed. Despite an overall conceptual understanding of piRNA biogenesis, identity and/or function of the involved players are largely unknown. Here, we demonstrate an essential role for the female sterility gene shutdown in piRNA biology. Shutdown, an evolutionarily conserved cochaperone collaborates with Hsp90 during piRNA biogenesis, potentially at the loading step of RNAs into PIWI proteins. We demonstrate that Shutdown is essential for both primary and secondary piRNA populations in Drosophila. An extension of our study to previously described piRNA pathway members revealed three distinct groups of biogenesis factors. Together with data on how PIWI proteins are wired into primary and secondary processing, we propose a unified model for piRNA biogenesis.
DOI 10.1016/j.molcel.2012.07.021
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Language of Publication English
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Publication Type Journal
Abbreviation Mol. Cell
Title Molecular Cell
Publication Year 1997-
ISBN/ISSN 1097-2765 1097-4164
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