Wood T F, Srivatsan E S, Chakrabarti R, Ma G C, Kuan N, Samara G J, Higgins M J, Shows T B, Johnson C L, Wan Y J, Passaro E P, Sawicki M P
Department of Surgery (W112), VAMC West Los Angeles, UCLA School of Medicine 90073, USA.
Genomics. 1996 Dec 1;38(2):166-73. doi: 10.1006/geno.1996.0612.
Linkage analysis and loss of heterozygosity studies have shown that the gene responsible for the multiple endocrine neoplasia type-1 (MEN1) syndrome localizes to a small interval between D11S427 and D11S460 on chromosome 11q13. As an initial step to clone this tumor suppressor gene, our group is the first to map the MEN1 region physically using yeast artificial chromosome, bacterial artificial chromosome (BAC), and cosmid contigs. The 1.5-Mb high-resolution, contiguous map extends from PYGM to 300 kb telomeric of D11S460. Of this, the 1.2-Mb interval between PYGM and D11S460 is isolated in cosmids and BACs and will be useful for the development of genomic sequences and transcription maps of this important region. Nine new sequence-tagged sites (STS) are also characterized from this region. The physical map and the STSs will be valuable tools for the cloning of the MEN1 gene.
连锁分析和杂合性缺失研究表明,导致多发性内分泌腺瘤1型(MEN1)综合征的基因定位于11号染色体11q13上D11S427和D11S460之间的一个小区域。作为克隆这个肿瘤抑制基因的第一步,我们小组率先使用酵母人工染色体、细菌人工染色体(BAC)和黏粒重叠群对MEN1区域进行物理图谱绘制。这个1.5兆碱基对的高分辨率连续图谱从PYGM延伸至D11S460端粒方向300千碱基对处。其中,PYGM和D11S460之间1.2兆碱基对的区域已通过黏粒和BAC分离出来,这将有助于构建该重要区域的基因组序列和转录图谱。该区域还鉴定出9个新的序列标签位点(STS)。物理图谱和STS将成为克隆MEN1基因的宝贵工具。