Targeted gene silencing in mouse germ cells by insertion of a homologous DNA into a piRNA generating locus

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Abstract

In germ cells, early embryos, and stem cells of animals, PIWI-interacting RNAs (piRNAs) have an important role in silencing retrotransposons, which are vicious genomic parasites, through transcriptional and post-transcriptional mechanisms. To examine whether the piRNA pathway can be used to silence genes of interest in germ cells, we have generated knock-in mice in which a foreign DNA fragment was inserted into a region generating pachytene piRNAs. The knock-in sequence was transcribed, and the resulting RNA was processed to yield piRNAs in postnatal testes. When reporter genes possessing a sequence complementary to portions of the knock-in sequence were introduced, they were greatly repressed after the time of pachytene piRNA generation. This repression mainly occurred at the post-transcriptional level, as degradation of the reporter RNAs was accelerated. Our results show that the piRNA pathway can be used as a tool for sequence-specific gene silencing in germ cells and support the idea that the piRNA generating regions serve as traps for retrotransposons, enabling the host cell to generate piRNAs against active retrotransposons. © 2013, Published by Cold Spring Harbor Laboratory Press.

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APA

Yamamoto, Y., Watanabe, T., Hoki, Y., Shirane, K., Li, Y., Ichiiyanagi, K., … Sasaki, H. (2013). Targeted gene silencing in mouse germ cells by insertion of a homologous DNA into a piRNA generating locus. Genome Research, 23(2), 292–299. https://doi.org/10.1101/gr.137224.112

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