QIP, a protein that converts duplex siRNA into single strands, is required for meiotic silencing by unpaired DNA

Hua Xiao, William G. Alexander, Thomas M. Hammond, Erin C. Boone, Tony D. Perdue, Patricia J. Pukkila, Patrick K.T. Shiu

Research output: Contribution to journalArticlepeer-review

37 Scopus citations

Abstract

RNA interference (RNAi) depends on the production of small RNA to regulate gene expression in eukaryotes. Two RNAi systems exist to control repetitive selfish elements in Neurospora crassa. Quelling targets transgenes during vegetative growth, whereas meiotic silencing by unpaired DNA (MSUD) silences unpaired genes during meiosis. The two mechanisms require common RNAi proteins, such as RNA-directed RNA polymerases, Dicers, and Argonaute slicers. We have previously demonstrated that, while Quelling depends on the redundant dicer activity of DCL-1 and DCL-2, only DCL-1 is required for MSUD. Here, we show that QDE-2-interacting protein (QIP), an exonuclease that is important for the production of single-stranded siRNA during Quelling, is also required for MSUD. QIP is crucial for sexual development and is shown to colocalize with other MSUD proteins in the perinuclear region.

Original languageEnglish
Pages (from-to)119-126
Number of pages8
JournalGenetics
Volume186
Issue number1
DOIs
StatePublished - Sep 2010
Externally publishedYes

Funding

FundersFunder number
National Science Foundation0918937

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