| Literature DB >> 24067652 |
Radha Raman Pandey1, Yoshimi Tokuzawa, Zhaolin Yang, Eri Hayashi, Tomoko Ichisaka, Shimpei Kajita, Yuka Asano, Tetsuo Kunieda, Ravi Sachidanandam, Shinichiro Chuma, Shinya Yamanaka, Ramesh S Pillai.
Abstract
Piwi-interacting RNAs (piRNAs) are gonad-specific small RNAs that provide defense against transposable genetic elements called transposons. Our knowledge of piRNA biogenesis is sketchy, partly due to an incomplete inventory of the factors involved. Here, we identify Tudor domain-containing 12 (TDRD12; also known as ECAT8) as a unique piRNA biogenesis factor in mice. TDRD12 is detected in complexes containing Piwi protein MILI (PIWIL2), its associated primary piRNAs, and TDRD1, all of which are already implicated in secondary piRNA biogenesis. Male mice carrying either a nonsense point mutation (reproductive mutant 23 or repro23 mice) or a targeted deletion in the Tdrd12 locus are infertile and derepress retrotransposons. We find that TDRD12 is dispensable for primary piRNA biogenesis but essential for production of secondary piRNAs that enter Piwi protein MIWI2 (PIWIL4). Cell-culture studies with the insect ortholog of TDRD12 suggest a role for the multidomain protein in mediating complex formation with other participants during secondary piRNA biogenesis.Entities:
Keywords: DNA methylation; helicase; spermatogenesis
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Year: 2013 PMID: 24067652 PMCID: PMC3799322 DOI: 10.1073/pnas.1316316110
Source DB: PubMed Journal: Proc Natl Acad Sci U S A ISSN: 0027-8424 Impact factor: 11.205