Sublocalization of the multiple endocrine neoplasia type 1 gene.

Henry Ford Hospital medical journal Pub Date : 1992-01-01
C Larsson, G Weber, M Janson
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Abstract

Tumorigenesis in multiple endocrine neoplasia type 1 (MEN 1) involves the unmasking of a recessive mutation at the MEN 1 locus which has been mapped to chromosomal region 11q11-13. By analyzing 58 DNA markers on a panel of radiation-reduced somatic cell hybrids, the region encompassing the MEN 1 gene was divided into nine subregions. Pulsed field gel electrophoresis analysis of markers within subgroups showed that the recombination rate around the MEN 1 locus is high. Combined linkage analysis in MEN 1 families and deletion mapping in MEN 1-related tumors suggest the MEN 1 gene is located centromeric to D11S807 and telomeric to PYGM.

多发性内分泌肿瘤1型基因的亚定位。
多发性内分泌肿瘤1型(MEN 1)的肿瘤发生涉及MEN 1位点的隐性突变,该突变已定位于染色体11q11-13区。通过分析辐射减少的体细胞杂交体上的58个DNA标记,将包含MEN 1基因的区域划分为9个亚区。亚群内标记的脉冲场凝胶电泳分析表明,MEN 1位点周围的重组率很高。结合对MEN 1家族的连锁分析和对MEN 1相关肿瘤的缺失定位表明,MEN 1基因的着丝粒定位于D11S807,端粒定位于PYGM。
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