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pubmed-article:1684084pubmed:abstractTextWe describe a high-resolution radiation hybrid map of the proximal long arm of human chromosome 11 containing the bcl-1 and multiple endocrine neoplasia type 1 (MEN-1) disease gene loci. We used X-ray irradiation and cell fusion to generate a panel of 102 hamster-human somatic cell hybrids containing fragments of human chromosome 11. Sixteen human loci in the 11q12-13 region were mapped by statistical analysis of the cosegregation of markers in these radiation hybrids. The most likely order for these loci is C1NH-OSBP-(CD5/CD20)-PGA-FTH1-COX8-PYGM -SEA-KRN1-(MTC/P11EH/HSTF1/INT2)-GST3- PPP1A. Our localization of the human protooncogene SEA between PYGM and INT2, two markers that flank MEN-1, suggests SEA as a potential candidate for the MEN-1 locus. We map two mitogenic fibroblast growth factor genes, HSTF1 and INT2, close to bcl-1, a mapping that is consistent with previously published data. Our map places the human leukocyte antigen genes CD5 and CD20 far from the bcl-1 locus, indicating that CD5 and CD20 expression is unlikely to be altered by bcl-1 rearrangements. PPP1A, which has been postulated as a MEN-1 candidate tumor suppressor gene, and GST3, a gene transcriptionally active in many human cancers, both map distal to the bcl-1 translocation cluster and the region containing MEN-1, and therefore are unlikely to be directly involved in bcl-1 or MEN-1.lld:pubmed
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pubmed-article:1684084pubmed:authorpubmed-author:CoxD RDRlld:pubmed
pubmed-article:1684084pubmed:authorpubmed-author:EvansG AGAlld:pubmed
pubmed-article:1684084pubmed:authorpubmed-author:RichardC...lld:pubmed
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pubmed-article:1684084pubmed:dateRevised2009-11-18lld:pubmed
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pubmed-article:1684084pubmed:articleTitleA radiation hybrid map of the proximal long arm of human chromosome 11 containing the multiple endocrine neoplasia type 1 (MEN-1) and bcl-1 disease loci.lld:pubmed
pubmed-article:1684084pubmed:affiliationDepartment of Psychiatry, University of California, San Francisco 94143-0554.lld:pubmed
pubmed-article:1684084pubmed:publicationTypeJournal Articlelld:pubmed
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