Genomic organization and assignment of VAMP2 to 17p12 by FISH.

G K Zoraqi, S Paradisi, V Falbo, D Taruscio
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引用次数: 2

Abstract

We describe the complete sequence, genomic organization, and FISH chromosome mapping of the human VAMP2. We identified a 7-kb clone, pISSHG2b3A, containing the entire structure of VAMP2. Previous studies performed by others identified a 5-kb clone, pVPC5-2, containing the incomplete VAMP2. The pVPC5-2 clone was partially sequenced and mapped to the broad region 17pter-->p12 by somatic cell hybridization. Our clone overlaps the pVPC5-2 clone and extends approximately 2 kb at the 3' end. In this study, we mapped this gene more precisely on 17p12 by FISH and we found a new polymorphic microsatellite, (GT)(7)CC(GT)(5), in exon V. This microsatellite, revealing three alleles with frequencies of 0.778, 0.139, and 0.083, might be useful for future linkage studies. Finally, we localized three previously known markers, stSG12859, TIGR-A002F11, and WIAF-1699 (alias stSG4044), in the 3' untranslated region of the gene.

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VAMP2到17p12的基因组组织和FISH定位。
我们描述了人类VAMP2的完整序列、基因组组织和FISH染色体定位。我们鉴定出一个7kb的克隆,pISSHG2b3A,包含VAMP2的整个结构。其他人先前的研究发现了一个5kb的克隆pVPC5-2,包含不完整的VAMP2。对pVPC5-2克隆进行了部分测序,并通过体细胞杂交定位到17pter- >p12宽区。我们的克隆与pVPC5-2克隆重叠,在3'端延伸约2kb。在这项研究中,我们通过FISH更精确地定位了该基因在17p12上的位置,并在v外显子上发现了一个新的多态性微卫星(GT)(7)CC(GT)(5),该微卫星揭示了三个频率分别为0.778,0.139和0.083的等位基因,可能对未来的连锁研究有用。最后,我们在基因的3'非翻译区定位了三个已知的标记,stSG12859, TIGR-A002F11和WIAF-1699(别名stSG4044)。
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