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pubmed-article:9272177pubmed:abstractTextThe multiple endocrine neoplasia type 1 (MEN1) locus has been previously localised to 11q13 by combined tumour deletion mapping and recombination studies, and a 0.5-Mb region, flanked by PYGM and D11S449, has been defined. In the course of constructing a conting, we have identified the location of the gene encoding the B56 beta subunit of protein phosphatase 2A (PP2A), which is involved in cell signal transduction pathways and thus represents a candidate gene for MEN1. We have searched for mutations in the PP2A-B56 beta coding region, together with the 5' and 3' untranslated regions in six MEN1 patients. DNA sequence abnormalities were not identified and thus the PP2A-B56 beta gene is excluded as the candidate gene for MEN1. However, our precise localisation of PP2A-B56 beta to this region of 11q13 may help in elucidating the basis for other disease genes mapping to this generich region.lld:pubmed
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pubmed-article:9272177pubmed:dateRevised2007-11-15lld:pubmed
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pubmed-article:9272177pubmed:articleTitleMapping of the gene encoding the B56 beta subunit of protein phosphatase 2A (PPP2R5B) to a 0.5-Mb region of chromosome 11q13 and its exclusion as a candidate gene for multiple endocrine neoplasia type 1 (MEN1).lld:pubmed
pubmed-article:9272177pubmed:affiliationMRC Molecular Endocrinology Group, Royal Postgraduate Medical School, Hammersmith Hospital, London, UK.lld:pubmed
pubmed-article:9272177pubmed:publicationTypeJournal Articlelld:pubmed
pubmed-article:9272177pubmed:publicationTypeResearch Support, Non-U.S. Gov'tlld:pubmed
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