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利用非整倍体人类淋巴细胞系进行基因剂量定位。

Mapping by gene dosage, using aneuploid human lymphoid cell lines.

作者信息

Soos M, Shade M, Bell H, Moxley M, Steel C M

出版信息

Ann Hum Genet. 1981 May;45(2):169-79. doi: 10.1111/j.1469-1809.1981.tb00319.x.

Abstract

Human lymphoblastoid cell lines evolve in vitro by the emergence of successive waves of clones which are often chromosomally marked. This offers the opportunity to compare tissue samples of the same genetic origin but differing in certain defined parts of the karyotype. Using selected sets of lines in which the members of genetically matched pairs differed in the number of copies of 8p or of 12p, levels of GSR and LDH B respectively have been shown to correlate with the specific chromosome aberrations, supporting existing data on the regional assignment of these two structural loci. This approach represents a useful addition to established methods for human gene mapping.

摘要

人类淋巴母细胞系在体外通过连续出现的克隆波进化,这些克隆通常具有染色体标记。这提供了比较具有相同遗传起源但核型某些特定部分不同的组织样本的机会。使用选定的细胞系组,其中基因匹配对的成员在8号染色体短臂或12号染色体短臂的拷贝数上有所不同,结果表明谷胱甘肽还原酶(GSR)和乳酸脱氢酶B(LDH B)的水平分别与特定的染色体畸变相关,这支持了关于这两个结构基因座区域定位的现有数据。这种方法是对已有的人类基因定位方法的有益补充。

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