The RNA-Binding ATPase, Armitage, Couples piRNA Amplification in Nuage to Phased piRNA Production on Mitochondria
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UMass Chan Affiliations
Graduate School of Biomedical SciencesProgram in Bioinformatics and Integrative Biology
RNA Therapeutics Institute
Document Type
Journal ArticlePublication Date
2019-06-06Keywords
ATPDTME
RNA-seq
argonaute
helicase
immunoprecipitation
mass spectrometry
microscopy
mitochondrion
small RNA
Amino Acids, Peptides, and Proteins
Biochemistry, Biophysics, and Structural Biology
Bioinformatics
Cell and Developmental Biology
Cells
Computational Biology
Enzymes and Coenzymes
Genetic Phenomena
Genetics and Genomics
Integrative Biology
Nucleic Acids, Nucleotides, and Nucleosides
Systems Biology
Metadata
Show full item recordAbstract
PIWI-interacting RNAs (piRNAs) silence transposons in Drosophila ovaries, ensuring female fertility. Two coupled pathways generate germline piRNAs: the ping-pong cycle, in which the PIWI proteins Aubergine and Ago3 increase the abundance of pre-existing piRNAs, and the phased piRNA pathway, which generates strings of tail-to-head piRNAs, one after another. Proteins acting in the ping-pong cycle localize to nuage, whereas phased piRNA production requires Zucchini, an endonuclease on the mitochondrial surface. Here, we report that Armitage (Armi), an RNA-binding ATPase localized to both nuage and mitochondria, links the ping-pong cycle to the phased piRNA pathway. Mutations that block phased piRNA production deplete Armi from nuage. Armi ATPase mutants cannot support phased piRNA production and inappropriately bind mRNA instead of piRNA precursors. We propose that Armi shuttles between nuage and mitochondria, feeding precursor piRNAs generated by Ago3 cleavage into the Zucchini-dependent production of Aubergine- and Piwi-bound piRNAs on the mitochondrial surface.Source
Mol Cell. 2019 Jun 6;74(5):982-995.e6. doi: 10.1016/j.molcel.2019.04.006. Epub 2019 May 7. Link to article on publisher's site
DOI
10.1016/j.molcel.2019.04.006Permanent Link to this Item
http://hdl.handle.net/20.500.14038/25858PubMed ID
31076285Related Resources
ae974a485f413a2113503eed53cd6c53
10.1016/j.molcel.2019.04.006
Scopus Count
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