Larsson C, Weber G, Janson M
Department of Clinical Genetics, Karolinska Hospital, Stockholm, Sweden.
Henry Ford Hosp Med J. 1992;40(3-4):159-61.
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.
1型多发性内分泌腺瘤病(MEN 1)的肿瘤发生涉及MEN 1基因座隐性突变的暴露,该基因座已被定位到染色体区域11q11 - 13。通过分析一组辐射减少的体细胞杂种上的58个DNA标记,包含MEN 1基因的区域被分为9个子区域。对亚组内标记的脉冲场凝胶电泳分析表明,MEN 1基因座周围的重组率很高。MEN 1家族中的联合连锁分析和MEN 1相关肿瘤中的缺失定位表明,MEN 1基因位于D11S807着丝粒侧和PYGM端粒侧。