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包含多发性内分泌腺瘤1型基因座的2.8兆碱基区域的转录图谱。

A transcript map for the 2.8-Mb region containing the multiple endocrine neoplasia type 1 locus.

作者信息

Guru S C, Agarwal S K, Manickam P, Olufemi S E, Crabtree J S, Weisemann J M, Kester M B, Kim Y S, Wang Y, Emmert-Buck M R, Liotta L A, Spiegel A M, Boguski M S, Roe B A, Collins F S, Marx S J, Burns L, Chandrasekharappa S C

出版信息

Genome Res. 1997 Jul;7(7):725-35. doi: 10.1101/gr.7.7.725.

Abstract

Multiple endocrine neoplasia type 1 (MEN 1) is an inherited cancer syndrome in which affected individuals develop multiple parathyroid, enteropancreatic, and pituitary tumors. The locus for MEN1 is tightly linked to the marker PYGM on chromosome 11q13, and linkage analysis places the MEN1 gene within a 2-Mb interval flanked by the markers D11S1883 and D11S449. Loss of heterozygosity studies in MEN 1 and sporadic tumors suggest that the MEN1 gene encodes a tumor suppressor and have helped to narrow the location of the gene to a 600-kb interval between PYGM and D11S449. Focusing on this smaller MEN1 interval, we have identified and mapped 12 transcripts to this 600-kb region. A precise ordered map of 33 transcripts, including 12 genes known to map to this region, was generated for the 2.8-Mb D11S480-D11S913 interval. Fifteen candidate genes (of which 10 were examined exhaustively) were evaluated by Southern blot and/or dideoxy fingerprinting analysis to identify the gene harboring disease-causing mutations.

摘要

多发性内分泌腺瘤1型(MEN 1)是一种遗传性癌症综合征,患病个体可发生多发性甲状旁腺、肠胰腺和垂体肿瘤。MEN1基因座与11号染色体11q13上的PYGM标记紧密连锁,连锁分析将MEN1基因定位在由D11S1883和D11S449标记侧翼的2 Mb区间内。对MEN 1和散发性肿瘤进行的杂合性缺失研究表明,MEN1基因编码一种肿瘤抑制因子,并有助于将该基因的位置缩小到PYGM和D11S449之间的600 kb区间。聚焦于这个较小的MEN1区间,我们已在这个600 kb区域内鉴定并定位了12个转录本。针对2.8 Mb的D11S480 - D11S913区间生成了包含33个转录本的精确有序图谱,其中包括已知定位到该区域的12个基因。通过Southern印迹和/或双脱氧指纹分析对15个候选基因(其中10个进行了详尽检测)进行评估,以鉴定携带致病突变的基因。

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