Su T S, Nussbaum R L, Airhart S, Ledbetter D H, Mohandas T, O'Brien W E, Beaudet A L
Am J Hum Genet. 1984 Sep;36(5):954-64.
There are multiple, processed, dispersed pseudogenes for human argininosuccinate synthetase. Chinese hamster X human somatic cell hybrids were used to map DNA fragment groups corresponding to the single expressed gene and 14 pseudogene loci. Each chromosomal assignment was confirmed using hybrids containing very few human chromosomes and/or by demonstrating monosomic or trisomic dosage in human cell lines with chromosomal abnormalities. Pseudogenes were mapped to chromosomes 2cen-p25, 3q12-qter, 4q21-qter, 5 (two loci), 6, 7, 9p13-q11, 9q11-q22, 11q, 12, Xp22-pter, Xq22-q26, and Ycen-q11. DNA fragments from the expressed gene were mapped to 9q34-qter in agreement with the previous assignment for enzyme activity. A high-frequency restriction fragment length polymorphism mapped to 9q11-q22. The analyses emphasized the feasibility of using chromosomally abnormal human cell lines for confirmation and regionalization of gene-mapping assignments made using somatic-cell hybrids. Conversely, cloned DNA probes, once mapped and characterized, can be very valuable for determining the chromosomal composition of interspecies hybrids and the dosage of loci in human cells. The argininosuccinate synthetase cDNA is a convenient reagent for dosage analysis of 15 human loci on 11 different chromosomes. Improved reagents could be designed that would simplify Southern blot patterns by eliminating overlapping DNA fragments and providing a single DNA fragment for each locus.
人类精氨琥珀酸合成酶存在多个经过加工、分散的假基因。利用中国仓鼠与人类体细胞杂种来定位与单个表达基因及14个假基因位点相对应的DNA片段组。使用含极少量人类染色体的杂种细胞,和/或通过在具有染色体异常的人类细胞系中证明单体或三体剂量,来确认每个染色体定位。假基因被定位到染色体2cen-p25、3q12-qter、4q21-qter、5(两个位点)、6、7、9p13-q11、9q11-q22、11q、12、Xp22-pter、Xq22-q26和Ycen-q11。来自表达基因的DNA片段与先前酶活性定位结果一致,被定位到9q34-qter。一个高频限制性片段长度多态性被定位到9q11-q22。这些分析强调了使用染色体异常的人类细胞系来确认和定位利用体细胞杂种所做基因定位的可行性。相反,一旦定位并鉴定,克隆的DNA探针对于确定种间杂种的染色体组成以及人类细胞中基因座的剂量非常有价值。精氨琥珀酸合成酶cDNA是用于分析11条不同染色体上15个人类基因座剂量的便利试剂。可以设计出改进的试剂,通过消除重叠的DNA片段并为每个基因座提供单个DNA片段来简化Southern印迹图谱。