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Positional candidate genes for congenital chloride diarrhea suggested by high-resolution physical mapping in chromosome region 7q31

机译:通过染色体区域7q31中的高分辨率物理作图提示先天性氯化物腹泻的位置候选基因

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摘要

Congenital chloride diarrhea affects intestinal transportation of electrolytes, resulting in potentially fatal diarrhea. Linkage disequilibrium analyses have suggested the congenital chloride diarrhea gene (CLD) to lie within 0.37 cM from D7S496 in human chromosome 7q31. To clone the CLD gene, we have constructed and refined a physical map based on a 2.7-Mb YAC contig around D7S496 and identified two candidate genes. The physical positions of 4 known genes (DRA, PRKAR2B, LAMB1, DLD), 7 polymorphic repeat markers, and 13 CpG islands were established. DRA (down-regulated in adenoma) is expressed in the gut and encodes a protein with sequence homology to anion transporters, whereas PRKAR2B encodes a regulatory subunit for protein kinase A. Both genes map within 450 kb from D7S496, making them functionally and positionally relevant candidates for CLD.
机译:先天性氯化物腹泻会影响电解质在肠道中的运输,从而导致潜在的致命性腹泻。连锁不平衡分析表明,先天性氯化物腹泻基因(CLD)位于人染色体7q31中距D7S496 0.37 cM之内。为了克隆CLD基因,我们基于D7S496周围的2.7 Mb YAC重叠群构建并完善了物理图谱,并鉴定了两个候选基因。建立了4个已知基因(DRA,PRKAR2B,LAMB1,DLD),7个多态性重复标记和13个CpG岛的物理位置。 DRA(在腺瘤中下调)在肠道中表达并编码与阴离子转运蛋白具有序列同源性的蛋白质,而PRKAR2B编码蛋白质激酶A的调节亚基。这两个基因均位于距D7S496 450 kb之内,从而使其在功能和位置上均具有相关性CLD的候选人。

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