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七个PAX基因的染色体定位及一个新家族成员PAX-9的克隆

Chromosomal localization of seven PAX genes and cloning of a novel family member, PAX-9.

作者信息

Stapleton P, Weith A, Urbánek P, Kozmik Z, Busslinger M

机构信息

Research Institute of Molecular Pathology, Vienna, Austria.

出版信息

Nat Genet. 1993 Apr;3(4):292-8. doi: 10.1038/ng0493-292.

Abstract

In the human paired box-containing (PAX) gene family, only two members, PAX-3 and PAX-6, which are associated with Waardenburg's syndrome and aniridia, respectively have been mapped to human chromosomes. We have now isolated cosmids for six additional human PAX genes (PAX-1,-2,-5,-7,-8,-9) and a polymerase chain reaction fragment for PAX-4. PAX-9 is a novel family member which is closely related in its paired domain to PAX-1. The chromosomal location of all cloned PAX genes was determined by analysis of somatic cell hybrids and (except PAX-4) by fluorescence in situ hybridization to metaphase chromosomes. PAX-1 and PAX-7 map to chromosomal regions containing previously assigned disease loci.

摘要

在人类含配对盒(PAX)基因家族中,只有分别与瓦登伯格综合征和无虹膜症相关的两个成员PAX - 3和PAX - 6已被定位到人类染色体上。我们现已分离出另外六个人类PAX基因(PAX - 1、- 2、- 5、- 7、- 8、- 9)的黏粒以及PAX - 4的聚合酶链反应片段。PAX - 9是一个新的家族成员,其配对结构域与PAX - 1密切相关。通过对体细胞杂种的分析以及(PAX - 4除外)通过与中期染色体的荧光原位杂交确定了所有克隆的PAX基因的染色体定位。PAX - 1和PAX - 7定位于含有先前确定的疾病基因座的染色体区域。

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