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dc.contributor.authorZhang, Donglei
dc.contributor.authorTu, Shikui
dc.contributor.authorStubna, Michael
dc.contributor.authorWu, Wei-Sheng
dc.contributor.authorHuang, Wei-Che
dc.contributor.authorWeng, Zhiping
dc.contributor.authorLee, Heng-Chi
dc.date2022-08-11T08:07:59.000
dc.date.accessioned2022-08-23T15:37:59Z
dc.date.available2022-08-23T15:37:59Z
dc.date.issued2018-02-02
dc.date.submitted2018-06-11
dc.identifier.citation<p>Science. 2018 Feb 2;359(6375):587-592. doi: 10.1126/science.aao2840. Epub 2018 Feb 1. <a href="https://doi.org/10.1126/science.aao2840">Link to article on publisher's site</a></p>
dc.identifier.issn0036-8075 (Linking)
dc.identifier.doi10.1126/science.aao2840
dc.identifier.pmid29420292
dc.identifier.urihttp://hdl.handle.net/20.500.14038/25840
dc.description.abstractPiwi-interacting RNAs (piRNAs) silence transposons to safeguard genome integrity in animals. However, the functions of the many piRNAs that do not map to transposons remain unknown. Here, we show that piRNA targeting in Caenorhabditis elegans can tolerate a few mismatches but prefer perfect pairing at the seed region. The broad targeting capacity of piRNAs underlies the germline silencing of transgenes in C. elegans Transgenes engineered to avoid piRNA recognition are stably expressed. Many endogenous germline-expressed genes also contain predicted piRNA targeting sites, and periodic An/Tn clusters (PATCs) are an intrinsic signal that provides resistance to piRNA silencing. Together, our study revealed the piRNA targeting rules and highlights a distinct strategy that C. elegans uses to distinguish endogenous from foreign nucleic acids.
dc.language.isoen_US
dc.relation<p><a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=29420292&dopt=Abstract">Link to Article in PubMed</a></p>
dc.relation.urlhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5939965/
dc.subjectBiochemistry, Biophysics, and Structural Biology
dc.subjectBioinformatics
dc.subjectComputational Biology
dc.titleThe piRNA targeting rules and the resistance to piRNA silencing in endogenous genes
dc.typeJournal Article
dc.source.journaltitleScience (New York, N.Y.)
dc.source.volume359
dc.source.issue6375
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/bioinformatics_pubs/131
dc.identifier.contextkey12289642
html.description.abstract<p>Piwi-interacting RNAs (piRNAs) silence transposons to safeguard genome integrity in animals. However, the functions of the many piRNAs that do not map to transposons remain unknown. Here, we show that piRNA targeting in Caenorhabditis elegans can tolerate a few mismatches but prefer perfect pairing at the seed region. The broad targeting capacity of piRNAs underlies the germline silencing of transgenes in C. elegans Transgenes engineered to avoid piRNA recognition are stably expressed. Many endogenous germline-expressed genes also contain predicted piRNA targeting sites, and periodic An/Tn clusters (PATCs) are an intrinsic signal that provides resistance to piRNA silencing. Together, our study revealed the piRNA targeting rules and highlights a distinct strategy that C. elegans uses to distinguish endogenous from foreign nucleic acids.</p>
dc.identifier.submissionpathbioinformatics_pubs/131
dc.contributor.departmentProgram in Bioinformatics and Integrative Biology
dc.source.pages587-592


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