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dc.contributor.authorMudhasani, Rajini R.
dc.contributor.authorPuri, Vishwajeet
dc.contributor.authorHoover, Kathleen
dc.contributor.authorCzech, Michael P.
dc.contributor.authorImbalzano, Anthony N.
dc.contributor.authorJones, Stephen N.
dc.date2022-08-11T08:09:15.000
dc.date.accessioned2022-08-23T16:24:00Z
dc.date.available2022-08-23T16:24:00Z
dc.date.issued2011-05-15
dc.date.submitted2011-01-28
dc.identifier.citationJ Cell Physiol. 2011 May;226(5):1399-406. doi: 10.1002/jcp.22475. <a href="http://dx.doi.org/10.1002/jcp.22475">Link to article on publisher's site</a>
dc.identifier.issn0021-9541 (Linking)
dc.identifier.doi10.1002/jcp.22475
dc.identifier.urihttp://hdl.handle.net/20.500.14038/36029
dc.description.abstractDicer, an enzyme involved in microRNA maturation, is required for proper embryo gastrulation and tissue morphogenesis during mammalian development. Using primary cultures of fibroblasts and pre-adipocytes, we have previously shown that Dicer is essential for early stages of adipogenic cell differentiation. In this present study, we have utilized Dicer-conditional mice to explore a role for Dicer and microRNA biogenesis in the terminal differentiation of adipocytes in vivo and in the formation of white and brown adipose tissue. Deletion of Dicer in differentiated adipocytes in Dicer-conditional, aP2-Cre transgenic mice reduced the level of various adipogenic-associated transcripts and inhibited lipogenesis in white adipocytes, resulting in a severe depletion of white adipose tissue in mice. In contrast, Dicer was not required in vivo for lipogenesis in brown adipose or for brown fat formation. However, Dicer deletion in brown adipose did decrease the expression of genes involved in thermoregulation. The results of our study provide genetic evidence of a role for microRNA molecules in regulating adipogenesis and reveal distinct requirements for Dicer in the formation of white and brown adipose tissue. (c) 2010 Wiley-Liss, Inc.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=pubmed&cmd=Retrieve&list_uids=20945399&dopt=Abstract">Link to Article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1002/jcp.22475
dc.subjectRibonuclease III
dc.subjectMicroRNAs
dc.subjectAdipocytes
dc.subjectAdipose Tissue, Brown
dc.subjectAdipose Tissue, White
dc.subjectCell Biology
dc.titleDicer is required for the formation of white but not brown adipose tissue
dc.typeJournal Article
dc.source.journaltitleJournal of cellular physiology
dc.source.volume226
dc.source.issue5
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/jones/4
dc.identifier.contextkey1750937
html.description.abstract<p>Dicer, an enzyme involved in microRNA maturation, is required for proper embryo gastrulation and tissue morphogenesis during mammalian development. Using primary cultures of fibroblasts and pre-adipocytes, we have previously shown that Dicer is essential for early stages of adipogenic cell differentiation. In this present study, we have utilized Dicer-conditional mice to explore a role for Dicer and microRNA biogenesis in the terminal differentiation of adipocytes in vivo and in the formation of white and brown adipose tissue. Deletion of Dicer in differentiated adipocytes in Dicer-conditional, aP2-Cre transgenic mice reduced the level of various adipogenic-associated transcripts and inhibited lipogenesis in white adipocytes, resulting in a severe depletion of white adipose tissue in mice. In contrast, Dicer was not required in vivo for lipogenesis in brown adipose or for brown fat formation. However, Dicer deletion in brown adipose did decrease the expression of genes involved in thermoregulation. The results of our study provide genetic evidence of a role for microRNA molecules in regulating adipogenesis and reveal distinct requirements for Dicer in the formation of white and brown adipose tissue. (c) 2010 Wiley-Liss, Inc.</p>
dc.identifier.submissionpathjones/4
dc.contributor.departmentProgram in Molecular Medicine
dc.contributor.departmentDepartment of Cell Biology
dc.source.pages1399-406


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