Minotaur is critical for primary piRNA biogenesis.

Minotaur is critical for primary piRNA biogenesis.
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DOI:
10.1261/rna.039669.113
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发表时间:
2013-08
期刊:
RNA (New York, N.Y.)
影响因子:
--
通讯作者:
Hannon GJ
Hannon GJ
中科院分区:
其他
文献类型:
--
作者:
Vagin VV;Yu Y;Jankowska A;Luo Y;Wasik KA;Malone CD;Harrison E;Rosebrock A;Wakimoto BT;Fagegaltier D;Muerdter F;Hannon GJ

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piRNA biogenesis remains poorly understood in any system. This paper provides evidence that glycerol-3-phosphate O-acetyltransferase is an unexpected factor required for piRNA biogenesis in Drosophila. Importantly, this enzyme, named Minotaur by the authors, when catalytically inactive due to mutations in the active site, retains function in piRNA biogenesis. Piwi proteins and their associated small RNAs are essential for fertility in animals. In part, this is due to their roles in guarding germ cell genomes against the activity of mobile genetic elements. piRNA populations direct Piwi proteins to silence transposon targets and, as such, form a molecular code that discriminates transposons from endogenous genes. Information ultimately carried by piRNAs is encoded within genomic loci, termed piRNA clusters. These give rise to long, single-stranded, primary transcripts that are processed into piRNAs. Despite the biological importance of this pathway, neither the characteristics that define a locus as a source of piRNAs nor the mechanisms that catalyze primary piRNA biogenesis are well understood. We searched an EMS-mutant collection annotated for fertility phenotypes for genes involved in the piRNA pathway. Twenty-seven homozygous sterile strains showed transposon-silencing defects. One of these, which strongly impacted primary piRNA biogenesis, harbored a causal mutation in CG5508, a member of the Drosophila glycerol-3-phosphate O-acetyltransferase (GPAT) family. These enzymes catalyze the first acylation step on the path to the production of phosphatidic acid (PA). Though this pointed strongly to a function for phospholipid signaling in the piRNA pathway, a mutant form of CG5508, which lacks the GPAT active site, still functions in piRNA biogenesis. We have named this new biogenesis factor Minotaur.
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