PIWI-interacting small RNAs: the vanguard of genome defence
By M. Siomi, Kaoru Sato, Dubravka Pezic, Alexei Aravin. Nature reviews. Molecular cell biology, 2011
1,305 citations recorded by the source corpus.
Subfields: Molecular Biology, Plant Science
View Paper: https://www.semanticscholar.org/paper/5ee62c75dd23b18554b6a2054f9cd9900c8c4e96
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In Molecular Biology
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In Plant Science
Citations in the corpus
- Long Noncoding RNAs: Past, Present, and Future (2013, background): “We refer readers to the many excellent recent reviews on these topics (Peculis 2000; Xiao et al. 2002; Henras et al. 2004; Okamura and Lai 2008; Kim et al. 2009; Feuerhahn et al. 2010; Blackburn and Collins 2011; Czech and Hannon 2011; Siomi et al. 2011).”
- A census of human RNA-binding proteins (2014, background): “The piRNA-PIWI complexes (piRNPs) silence transposable elements (TEs) either by endonucleolytic cleavage in the cytoplasm or through transcriptional silencing at their genomic loci in the nucleus (Siomi et al., 2011).”
- Transcriptional and Post-transcriptional Gene Regulation by Long Non-coding RNA (2017, background): “Short ncRNAs include the relatively wellknown microRNAs (miRNAs) [9,10], as well as smallinterfering RNAs (siRNAs) and P-element-induced wimpy testis (PIWI)-interacting RNA (piRNAs) [11], which generally act to negatively regulate gene expression.”
- CRISPR-Cas systems in bacteria and archaea: versatile small RNAs for adaptive defense and regulation. (2011, background): “Overall, although CRISPR is arguably most similar to PIWI-interacting RNAs (piRNAs), which protect genome integrity from parasites such as transposons (103), further studies that examine the molecular basis for CRISPR-based interference will likely expand the list of mechanistic idiosyncrasies and n”
- Transcriptional Silencing of Transposons by Piwi and Maelstrom and Its Impact on Chromatin State and Gene Expression (2012, neutral): “…sequence for mael was CCGAAGCTTGTTCGCTTTCTA y,w,hsFlp122;;act<CD2>GAL4, UAS-GFP (Olivieri et al, 2010) FLAG-eGFP-Mael was cloned by inserting an N-terminal FLAG-eGFP cassette via bacterial recombineering into a genomic rescue construct (3L : 22712955 -22721349) which was integrated into the…”