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将达里埃病基因座精细定位到12号染色体q24.1区域小于1厘摩的范围内,并构建关键区域完整的高分辨率P1人工染色体/细菌人工染色体重叠群。

Refined genetic mapping of the darier locus to a <1-cM region of chromosome 12q24.1, and construction of a complete, high-resolution P1 artificial chromosome/bacterial artificial chromosome contig of the critical region.

作者信息

Monk S, Sakuntabhai A, Carter S A, Bryce S D, Cox R, Harrington L, Levy E, Ruiz-Perez V L, Katsantoni E, Kodvawala A, Munro C S, Burge S, Larrègue M, Nagy G, Rees J L, Lathrop M, Monaco A P, Strachan T, Hovnanian A

机构信息

Wellcome Trust Centre for Human Genetics, University of Oxford, Headington, Oxford, OX3 7BN, United Kingdom.

出版信息

Am J Hum Genet. 1998 Apr;62(4):890-903. doi: 10.1086/301794.

Abstract

Darier disease (DD) (MIM 124200) is an autosomal dominant skin disorder characterized by loss of adhesion between epidermal cells and by abnormal keratinization. We present linkage analysis showing, in four families, key recombination events that refine the location of the DD locus on chromosome 12q23-24.1 to a region of <1 cM. We have constructed a YAC/P1 artificial chromosome (PAC)/bacterial artificial chromosome (BAC)-based physical map that encompasses this refined DD region. The map consists of 35 YAC, 69 PAC, 16 BAC, and 2 cosmid clones that were ordered by mapping 54 anonymous sequence-tagged sites. The critical region is estimated to be 2.4 Mb in size, with an average marker resolution of 37.5 kb. The refinement of the critical interval excludes the ALDH2, RPL6, PTPN11, and OAS genes, as well as seven expressed sequence tags (ESTs) previously mapped in the DD region. The three known genes (ATP2A2, PPP1CC, and SCA2) and the 10 ESTs mapped within the critical region are not obvious candidates for the DD gene. Therefore, this detailed integrated physical, genetic, and partial transcript map provides an important resource for the isolation of the DD gene and, possibly, other disease genes.

摘要

毛囊角化病(DD)(MIM 124200)是一种常染色体显性遗传性皮肤病,其特征为表皮细胞间黏附丧失和异常角化。我们进行了连锁分析,在四个家系中发现了关键的重组事件,这些事件将DD基因座在12号染色体q23 - 24.1上的定位精确到了小于1厘摩的区域。我们构建了一个基于酵母人工染色体(YAC)/P1人工染色体(PAC)/细菌人工染色体(BAC)的物理图谱,该图谱涵盖了这个精确的DD区域。该图谱由35个YAC、69个PAC、16个BAC和2个黏粒克隆组成,通过对54个匿名序列标签位点进行定位来排序。关键区域估计大小为2.4兆碱基对,平均标记分辨率为37.5千碱基对。关键区间的精确划分排除了醛脱氢酶2(ALDH2)、核糖体蛋白L6(RPL6)、蛋白酪氨酸磷酸酶非受体型11(PTPN11)和2'-5'-寡腺苷酸合成酶(OAS)基因,以及先前定位在DD区域的7个表达序列标签(EST)。在关键区域内定位的三个已知基因(ATP2A2、蛋白磷酸酶1催化亚基γ(PPP1CC)和脊髓小脑共济失调2型(SCA2))和10个EST并非DD基因的明显候选基因。因此,这个详细的综合物理、遗传和部分转录图谱为分离DD基因以及可能的其他疾病基因提供了重要资源。

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