Please use this identifier to cite or link to this item: http://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/6210
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dc.contributor.authorDeshmukh, Prachien_US
dc.contributor.authorMarkande, Shubhaen_US
dc.contributor.authorFandade, Vikasen_US
dc.contributor.authorRAMTIRTHA, YOGENDRAen_US
dc.contributor.authorMADHUSUDHAN, M. S.en_US
dc.contributor.authorJoseph, Jomonen_US
dc.date.accessioned2021-08-27T11:21:37Z
dc.date.available2021-08-27T11:21:37Z
dc.date.issued2021-06en_US
dc.identifier.citationBiochemical and Biophysical Research Communications, 556, 45-52.en_US
dc.identifier.issn0006-291Xen_US
dc.identifier.urihttp://dr.iiserpune.ac.in:8080/xmlui/handle/123456789/6210
dc.identifier.urihttps://doi.org/10.1016/j.bbrc.2021.03.140en_US
dc.description.abstractMicro-RNA mediated suppression of mRNA translation represents a major regulatory mode of post-transcriptional gene expression. Recently, the nucleoporin Nup358 was shown to interact with AGO protein, a key component of miRNA-induced silencing complex (miRISC), and facilitate the coupling of miRISC with target mRNA. Previous results suggested that SUMO-interacting motifs (SIMs) present on Nup358 mediate interaction with AGO protein. Here we show that Nup358-SIM has multiple interacting regions on AGO2, specifically within the N, PAZ and MID domains, with an affinity comparable to SIM-SUMO1 interaction. The study also unraveled specific residues involved in the interaction of AGO2 with miRNA-loading components such as Dicer and HSP90. Collectively, the results support the conclusion that multiple SIMs contribute to the association of Nup358 with AGO2.en_US
dc.language.isoenen_US
dc.publisherElsevier B.V.en_US
dc.subjectmiRNAen_US
dc.subjectNup358en_US
dc.subjectSUMO-interaction motifen_US
dc.subjectAGO2en_US
dc.subjectDiceren_US
dc.subjectHsp90en_US
dc.subject2021-AUG-WEEK4en_US
dc.subject2021en_US
dc.titleThe miRISC component AGO2 has multiple binding sites for Nup358 SUMO-interacting motifen_US
dc.typeArticleen_US
dc.contributor.departmentDept. of Biologyen_US
dc.identifier.sourcetitleBiochemical and Biophysical Research Communicationsen_US
dc.publication.originofpublisherForeignen_US
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