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小鼠中脯氨酰肽酶(PEP - 4)的基因变异定位在7号染色体上葡萄糖磷酸异构酶(GPI - 1)基因附近。

Genetic variation for prolidase (PEP-4) in the mouse maps near the gene for glucosephosphate isomerase (GPI-1) on chromosome 7.

作者信息

Skow L C

出版信息

Biochem Genet. 1981 Aug;19(7-8):695-700. doi: 10.1007/BF00484002.

Abstract

An inherited electrophoretic variant of prolidase (EC 3.4.13.9), also called peptidase 4 (PEP-4), has been discovered among inbred strains of mice. Analysis of progeny from reciprocal backcrosses established that the electrophoretic forms are expressed codominantly and that Pep-4 is located between the genes for glucosephosphate isomerase (Gpi-1) and pink-eyed dilution (p) on chromosome 7. These data define a region of conserved gene linkage between mouse chromosome 7 and human chromosome 19, as originally indicated by somatic cell hybrid studies, and imply that human prolidase (PEPD) is located in the region of human chromosome 19 pter greater than q13.

摘要

在近交系小鼠中发现了一种脯氨酰二肽酶(EC 3.4.13.9,也称为肽酶4,即PEP-4)的遗传性电泳变体。对正反交回交子代的分析表明,电泳形式呈共显性表达,且Pep-4基因位于7号染色体上的葡萄糖磷酸异构酶(Gpi-1)基因和粉红眼稀释(p)基因之间。这些数据确定了小鼠7号染色体和人类19号染色体之间保守的基因连锁区域,正如体细胞杂交研究最初所表明的那样,这意味着人类脯氨酰二肽酶(PEPD)位于人类19号染色体短臂大于q13的区域。

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