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10.1038/nmeth.4121

http://scihub22266oqcxt.onion/10.1038/nmeth.4121
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C5423094!5423094!28024160
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suck abstract from ncbi


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pmid28024160      Nat+Methods 2017 ; 14 (2): 201-7
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  • RESA identifies mRNA regulatory sequences with high resolution #MMPMID28024160
  • Yartseva V; Takacs CM; Vejnar CE; Lee MT; Giraldez AJ
  • Nat Methods 2017[Feb]; 14 (2): 201-7 PMID28024160show ga
  • Gene expression is regulated extensively at the level of mRNA stability, localization, and translation. However, decoding functional RNA regulatory features remains a limitation to understanding post-transcriptional regulation in vivo. Here, we developed RNA Element Selection Assay (RESA), a method that selects RNA elements based on their activity in vivo and uses high-throughput sequencing to provide quantitative measurement of their regulatory function with near nucleotide resolution. We implemented RESA to identify sequence elements modulating mRNA stability during zebrafish embryogenesis. RESA provides a sensitive and quantitative measure of microRNA activity in vivo and also identifies novel regulatory sequences. To uncover specific sequence requirements within regulatory elements, we developed a bisulfite-mediated nucleotide conversion strategy for large-scale mutational analysis (RESA-bisulfite). Finally, we used the versatile RESA platform to map candidate protein-RNA interactions in vivo (RESA-CLIP). The RESA platform can be broadly applicable to uncover the regulatory features shaping gene expression and cellular function.
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