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pubmed-article:7606786pubmed:abstractTextLipomas are one of the most common mesenchymal neoplasms in humans. They are characterized by consistent cytogenetic aberrations involving chromosome 12 in bands q14-15. Interestingly, this region is also the site of rearrangement for other mesenchymally derived tumors. This study demonstrates that HMGI-C, an architectural factor that functions in transcriptional regulation, has been disrupted by rearrangement at the 12q14-15 chromosomal breakpoint in lipomas. Chimeric transcripts were isolated from two lipomas in which HMGI-C DNA-binding domains (AT hook motifs) are fused to either a LIM or an acidic transactivation domain. These results, identifying a gene rearranged in a benign neoplastic process that does not proceed to a malignancy, suggest a role for HMGI-C in adipogenesis and mesenchyme differentiation.lld:pubmed
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pubmed-article:7606786pubmed:articleTitleDisruption of the architectural factor HMGI-C: DNA-binding AT hook motifs fused in lipomas to distinct transcriptional regulatory domains.lld:pubmed
pubmed-article:7606786pubmed:affiliationDepartment of Biochemistry, Robert Wood Johnson Medical School, University of Medicine and Dentistry of New Jersey, Piscataway 08854, USA.lld:pubmed
pubmed-article:7606786pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:7606786pubmed:publicationTypeResearch Support, U.S. Gov't, P.H.S.lld:pubmed
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