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dc.contributor.authorMcGeary, Sean E
dc.contributor.authorBisaria, Namita
dc.contributor.authorPham, Thy M
dc.contributor.authorWang, Peter Y
dc.contributor.authorBartel, David P
dc.date.accessioned2022-12-06T17:15:32Z
dc.date.available2022-12-06T17:15:32Z
dc.date.issued2022
dc.identifier.urihttps://hdl.handle.net/1721.1/146764
dc.description.abstract<jats:p>MicroRNAs (miRNAs), in association with Argonaute (AGO) proteins, direct repression by pairing to sites within mRNAs. Compared to pairing preferences of the miRNA seed region (nucleotides 2–8), preferences of the miRNA 3′ region are poorly understood, due to the sparsity of measured affinities for the many pairing possibilities. We used RNA bind-n-seq with purified AGO2–miRNA complexes to measure relative affinities of &gt;1000 3′-pairing architectures for each miRNA. In some cases, optimal 3′ pairing increased affinity by &gt;500 fold. Some miRNAs had two high-affinity 3′-pairing modes—one of which included additional nucleotides bridging seed and 3′ pairing to enable high-affinity pairing to miRNA nucleotide 11. The affinity of binding and the position of optimal pairing both tracked with the occurrence of G or oligo(G/C) nucleotides within the miRNA. These and other results advance understanding of miRNA targeting, providing insight into how optimal 3′ pairing is determined for each miRNA.</jats:p>en_US
dc.language.isoen
dc.publishereLife Sciences Publications, Ltden_US
dc.relation.isversionof10.7554/ELIFE.69803en_US
dc.rightsCreative Commons Attribution 4.0 International licenseen_US
dc.rights.urihttps://creativecommons.org/licenses/by/4.0/en_US
dc.sourceeLifeen_US
dc.titleMicroRNA 3′-compensatory pairing occurs through two binding modes, with affinity shaped by nucleotide identity and positionen_US
dc.typeArticleen_US
dc.identifier.citationMcGeary, Sean E, Bisaria, Namita, Pham, Thy M, Wang, Peter Y and Bartel, David P. 2022. "MicroRNA 3′-compensatory pairing occurs through two binding modes, with affinity shaped by nucleotide identity and position." eLife, 11.
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biology
dc.contributor.departmentWhitehead Institute for Biomedical Research
dc.contributor.departmentHoward Hughes Medical Institute
dc.relation.journaleLifeen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2022-12-06T16:44:36Z
dspace.orderedauthorsMcGeary, SE; Bisaria, N; Pham, TM; Wang, PY; Bartel, DPen_US
dspace.date.submission2022-12-06T16:44:37Z
mit.journal.volume11en_US
mit.licensePUBLISHER_CC
mit.metadata.statusAuthority Work and Publication Information Neededen_US


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