Please use this identifier to cite or link to this item: https://doi.org/10.2337/db17-0655
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dc.titleRNA binding protein Ybx2 regulates RNA stability during cold-induced brown fat activation
dc.contributor.authorXu D.
dc.contributor.authorXu S.
dc.contributor.authorKyaw A.M.M.
dc.contributor.authorLim Y.C.
dc.contributor.authorChia S.Y.
dc.contributor.authorSiang D.T.C.
dc.contributor.authorAlvarez-Dominguez J.R.
dc.contributor.authorChen P.
dc.contributor.authorKhee-Shing Leow M.
dc.contributor.authorSun L.
dc.date.accessioned2020-10-15T04:28:57Z
dc.date.available2020-10-15T04:28:57Z
dc.date.issued2017
dc.identifier.citationXu D., Xu S., Kyaw A.M.M., Lim Y.C., Chia S.Y., Siang D.T.C., Alvarez-Dominguez J.R., Chen P., Khee-Shing Leow M., Sun L. (2017). RNA binding protein Ybx2 regulates RNA stability during cold-induced brown fat activation. Diabetes 66 (12) : 2987 - 3000. ScholarBank@NUS Repository. https://doi.org/10.2337/db17-0655
dc.identifier.issn0012-1797
dc.identifier.urihttps://scholarbank.nus.edu.sg/handle/10635/177489
dc.description.abstractRecent years have seen an upsurge of interest in brown adipose tissue (BAT) to combat the epidemic of obesity and diabetes. How its development and activation are regulated at the posttranscriptional level, however, has yet to be fully understood. RNA binding proteins (RBPs) lie in the center of posttranscriptional regulation. To systemically study the role of RBPs in BAT, we profiled >400 RBPs in different adipose depots and identified Y-box binding protein 2 (Ybx2) as a novel regulator in BAT activation. Knockdown of Ybx2 blocks brown adipogenesis, whereas its overexpression promotes BAT marker expression in brown and white adipocytes. Ybx2-knockout mice could form BAT but failed to express a full thermogenic program. Integrative analysis of RNA sequencing and RNA-immunoprecipitation study revealed a set of Ybx2's mRNA targets, including Pgc1a, that were destabilized by Ybx2 depletion during cold-induced activation. Thus, Ybx2 is a novel regulator that controls BAT activation by regulating mRNA stability.
dc.publisherAmerican Diabetes Association Inc.
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentDUKE-NUS MEDICAL SCHOOL
dc.description.doi10.2337/db17-0655
dc.description.sourcetitleDiabetes
dc.description.volume66
dc.description.issue12
dc.description.page2987 - 3000
dc.published.statePublished
dc.grant.idNRF-2011NRF-NRFF 001-025
dc.grant.idNMRC/CBRG/0101/2016
dc.grant.idNMRC/CBRG/0070/2014
dc.grant.fundingagencyNational Research Foundation Singapore,�NRF
dc.grant.fundingagencyNational Medical Research Council,�NMRC
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