A somatic piRNA pathway in the Drosophila fat body ensures metabolic homeostasis and normal lifespan

Brian C. Jones, Jason G. Wood, Chengyi Chang, Austin D. Tam, Michael J. Franklin, Emily R. Siegel and Stephen L. Helfand ()
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Brian C. Jones: Cell Biology, and Biochemistry, Brown University
Jason G. Wood: Cell Biology, and Biochemistry, Brown University
Chengyi Chang: Cell Biology, and Biochemistry, Brown University
Austin D. Tam: Cell Biology, and Biochemistry, Brown University
Michael J. Franklin: Cell Biology, and Biochemistry, Brown University
Emily R. Siegel: Cell Biology, and Biochemistry, Brown University
Stephen L. Helfand: Cell Biology, and Biochemistry, Brown University

Nature Communications, 2016, vol. 7, issue 1, 1-9

Abstract: Abstract In gonadal tissues, the Piwi-interacting (piRNA) pathway preserves genomic integrity by employing 23–29 nucleotide (nt) small RNAs complexed with argonaute proteins to suppress parasitic mobile sequences of DNA called transposable elements (TEs). Although recent evidence suggests that the piRNA pathway may be present in select somatic cells outside the gonads, the role of a non-gonadal somatic piRNA pathway is not well characterized. Here we report a functional somatic piRNA pathway in the adult Drosophila fat body including the presence of the piRNA effector protein Piwi and canonical 23–29 nt long TE-mapping piRNAs. The piwi mutants exhibit depletion of fat body piRNAs, increased TE mobilization, increased levels of DNA damage and reduced lipid stores. These mutants are starvation sensitive, immunologically compromised and short-lived, all phenotypes associated with compromised fat body function. These findings demonstrate the presence of a functional non-gonadal somatic piRNA pathway in the adult fat body that affects normal metabolism and overall organismal health.

Date: 2016
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DOI: 10.1038/ncomms13856

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