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5号染色体上家族性腺瘤性息肉病基因周围六个多态性DNA标记的遗传连锁图谱。

Genetic linkage map of six polymorphic DNA markers around the gene for familial adenomatous polyposis on chromosome 5.

作者信息

Dunlop M G, Wyllie A H, Nakamura Y, Steel C M, Evans H J, White R L, Bird C C

机构信息

Medical Research Council Human Genetics Unit, Western General Hospital, Edinburgh, Scotland.

出版信息

Am J Hum Genet. 1990 Dec;47(6):982-7.

Abstract

A genetic linkage map of six polymorphic DNA markers close to the gene (APC) for familial adenomatous polyposis (FAP) on chromosome 5q is reported. One hundred fifty-five typed members of nine FAP kindred provided more than 90 meioses for linkage analysis. A number of crucial recombination events have been identified which are informative at three or more loci, allowing confident ordering of parts of the map. There was no evidence of genetic heterogeneity, with all families showing linkage of at least one chromosome 5 marker to the gene. Recombination data and two-point linkage analysis support a locus order of centromere-pi 227-C11P11-ECB27-L5.62-APC-EF5.44-YN5.48-telomer e, although EF5.44 could lie in the interval L5.62-APC or ECB27-L5.62. No recombinants were identified between APC and either EF5.44 or YN5.48, but published deletion mapping in colorectal carcinomas and linkage analysis in FAP suggest that YN5.48 is 1-3 cM from APC. The present study suggests that YN5.48 and L5.62 delineate a small region of chromosome 5 within which the EF5.44 locus lies very close to the APC gene. These data not only allow use of flanking markers for presymptomatic diagnosis of FAP but also provide a high-density map of the region for isolation of the APC gene itself and for further assessment of the role of chromosome 5 deletions in the biology of sporadic colorectal cancer.

摘要

报道了位于5号染色体上与家族性腺瘤性息肉病(FAP)基因(APC)紧密连锁的6个多态性DNA标记的遗传连锁图谱。9个FAP家系的155名分型成员提供了90多个减数分裂用于连锁分析。已鉴定出一些关键的重组事件,这些事件在三个或更多位点上具有信息性,从而能够确定图谱部分的可靠顺序。没有遗传异质性的证据,所有家系均显示至少一个5号染色体标记与该基因连锁。重组数据和两点连锁分析支持着丝粒-pi 227-C11P11-ECB27-L5.62-APC-EF5.44-YN5.48-端粒的基因座顺序,尽管EF5.44可能位于L5.62-APC区间或ECB27-L5.62区间。在APC与EF5.44或YN5.48之间未鉴定出重组体,但已发表的结直肠癌缺失图谱和FAP中的连锁分析表明YN5.48距APC为1-3厘摩。本研究表明YN5.48和L5.62划定了5号染色体的一个小区域,其中EF5.44基因座非常靠近APC基因。这些数据不仅允许使用侧翼标记对FAP进行症状前诊断,而且还提供了该区域的高密度图谱,用于APC基因本身的分离以及进一步评估5号染色体缺失在散发性结直肠癌生物学中的作用。

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