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D5S71位点上新的缺失多态性增加了腺瘤性息肉病基因的连锁信息:对症状前诊断的意义。

A new deletion polymorphism at D5S71 raises the linkage information on adenomatous polyposis coli: implications for presymptomatic diagnosis.

作者信息

Tops C M, Breukel C, van der Klift H M, von Leeuwen I S, Wijnen J T, Griffioen G, Vasen H F, den Hartog Jager F C, Nagengast F M, Lamers C B

机构信息

Human Genetics Institute, University of Leiden, The Netherlands.

出版信息

Hum Genet. 1991 Feb;86(4):365-8. doi: 10.1007/BF00201835.

Abstract

Two independent study-groups, one in Britain and the other in the United States, were the first to report linkage between APC and a TaqI restriction fragment length polymorphism (RFLP) at D5S71 (probe C11p11) on chromosome 5q. They found no recombinants in about 50 informative meioses. The same TaqI RFLP was found to be uninformative for linkage in 15 Dutch polyposis families. The recently reported four base-pair deletion polymorphism (DEL1) at D5S71 has raised the polymorphism information content of this marker from 0.17 to 0.40 in the Dutch population. Seven of 20 polyposis families screened for the DEL1 as well as the TaqI polymorphism gave a combined peak lod score of 5.68 with no recombinants in 37 informative meioses. These data, together with those so far reported in the literature, raise the peak lod score to 17.09 at a recombination fraction of 0.05, the 95% upper confidence limit being 0.09. In combination with the use of another informative marker, D5S81 (probe YN5.48) closely mapping on the other side of APC, the presymptomatic diagnosis of the disease can be made with more than 99.9% certainty. It has to be stressed, however, that the the possible existence of more than one polyposis locus cannot, as yet, be excluded.

摘要

两个独立的研究小组,一个在英国,另一个在美国,率先报道了位于5号染色体5q上D5S71(探针C11p11)处的APC与TaqI限制性片段长度多态性(RFLP)之间的连锁关系。他们在约50个信息减数分裂中未发现重组体。在15个荷兰息肉病家族中,发现相同的TaqI RFLP对于连锁分析无信息价值。最近报道的D5S71处的四碱基对缺失多态性(DEL1)使该标记在荷兰人群中的多态性信息含量从0.17提高到了0.40。在筛查DEL1以及TaqI多态性的20个息肉病家族中,有7个家族在37个信息减数分裂中无重组体,联合峰值lod分数为5.68。这些数据,连同文献中迄今为止报道的数据,在重组率为0.05时将峰值lod分数提高到了17.09,95%的置信上限为0.09。结合使用另一个信息性标记D5S81(探针YN5.48),其紧密定位在APC的另一侧,疾病的症状前诊断确定性可超过99.9%。然而,必须强调的是,目前尚不能排除可能存在不止一个息肉病基因座。

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