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小鼠组氨酸血症(his)突变的鉴定及小鼠组氨酸酶基因座(Hal)在10号染色体上的基因定位。

Identification of the mutation in murine histidinemia (his) and genetic mapping of the murine histidase locus (Hal) on chromosome 10.

作者信息

Taylor R G, Grieco D, Clarke G A, McInnes R R, Taylor B A

机构信息

Department of Molecular and Medical Genetics, University of Toronto, Ontario, Canada.

出版信息

Genomics. 1993 Apr;16(1):231-40. doi: 10.1006/geno.1993.1164.

Abstract

We cloned a mouse histidase cDNA to identify the mutation in histidinemic mice (his/his) and to determine the relationship of the histidase locus (Hal) both to Chromosome 10 markers and to Hsd, the histidase activity variant locus. The his mutation, a G to A transition at nucleotide +965, changes Arg-322 to Gln (R322Q). Expression of the R322Q allele in COS cells resulted in proportionately reduced amounts of histidase protein and activity compared to the wildtype allele. Hal maps approximately 4 cM distal to the insulin-like growth factor-1 locus and approximately 10 cM proximal to steel. Hsd was found to be tightly linked to Hal, and the low-histidase-activity Hsd allele was associated with reduced histidase mRNA. These studies indicate that the R322Q allele reduces the stability of histidase, position Hal on the Chromosome 10 linkage map, and provide further evidence that Hsd is allelic to Hal.

摘要

我们克隆了小鼠组氨酸酶cDNA,以鉴定组氨酸血症小鼠(his/his)中的突变,并确定组氨酸酶基因座(Hal)与10号染色体标记以及组氨酸酶活性变异基因座Hsd之间的关系。his突变是核苷酸+965处的G到A转换,将Arg-322变为Gln(R322Q)。与野生型等位基因相比,R322Q等位基因在COS细胞中的表达导致组氨酸酶蛋白和活性的量相应减少。Hal位于胰岛素样生长因子-1基因座远端约4 cM处,位于Steel近端约10 cM处。发现Hsd与Hal紧密连锁,低组氨酸酶活性的Hsd等位基因与组氨酸酶mRNA减少有关。这些研究表明,R322Q等位基因降低了组氨酸酶的稳定性,在10号染色体连锁图谱上定位了Hal,并提供了进一步的证据表明Hsd与Hal是等位基因。

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