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人-鼠及猴-鼠体细胞杂种中线粒体胸苷激酶的遗传控制

Genetic control of mitochondrial thymidine kinase in human-mouse and monkey-mouse somatic cell hybrids.

作者信息

Kit S, Leung W C

出版信息

J Cell Biol. 1974 Apr;61(1):35-44. doi: 10.1083/jcb.61.1.35.

Abstract

Distinctive thymidine (dT) kinase molecular forms are present in mouse, human, and monkey mitochondria. Disk polyacrylamide gel electrophoresis (disk PAGE) analyses have shown that the mitochondrial-specific dT kinases differ from cytosol dT kinases in relative electrophoretic mobilities (Rm). Furthermore, the mouse mitochondrial dT kinase differs in Rm value from primate mitochondrial dT kinases. The mouse and primate cytosol dT kinases can also be distinguished. Disk PAGE analyses have been carried out on the cytosol and mitochondrial dT kinases of human-mouse (WIL-8) and monkey-mouse (mK.CV(III)) somatic cell hybrids in order to learn whether the mitochondria of the hybrid cells contained murine mitochondrial-specific, primate mitochondrial-specific, or both dT kinases. WIL-8 cells were derived from cytosol dT kinase-negative, mitochondrial dT kinase-positive mouse fibro blasts and from cytosol dT kinase-positive, mitochondrial dT kinase-positive human embryonic lung cells; they contained mostly mouse chromosomes and a few human chromosomes, including the determinant for human cytosol dT kinase. The mK.CV(III) cells were derived from cytosol dT kinase-negative, mitochondrial dT kinase-positive mouse kidney cells and from cytosol dT kinase-positive, mitochondrial dT kinase-positive monkey kidney cells; they contained mostly mouse chromosomes and a few monkey chromosomes, including the determinant for monkey cytosol dT kinase. Disk PAGE analyses demonstrated that the mitochondria of human-mouse and monkey-mouse somatic cell hybrids contained the mouse-specific mitochondrial dT kinase but not the human- or monkey-specific mitochondrial dT kinase. These findings suggest that primate cytosol and mitochondrial thymidine kinase genes are coded on different chromosomes.

摘要

在小鼠、人类和猴子的线粒体中存在独特的胸苷激酶分子形式。圆盘聚丙烯酰胺凝胶电泳(圆盘PAGE)分析表明,线粒体特异性胸苷激酶在相对电泳迁移率(Rm)方面与胞质胸苷激酶不同。此外,小鼠线粒体胸苷激酶的Rm值与灵长类动物线粒体胸苷激酶不同。小鼠和灵长类动物的胞质胸苷激酶也可以区分。为了了解杂交细胞的线粒体中是否含有小鼠线粒体特异性、灵长类动物线粒体特异性或两种胸苷激酶,对人 - 小鼠(WIL - 8)和猴 - 小鼠(mK.CV(III))体细胞杂种的胞质和线粒体胸苷激酶进行了圆盘PAGE分析。WIL - 8细胞来源于胞质胸苷激酶阴性、线粒体胸苷激酶阳性的小鼠成纤维细胞和胞质胸苷激酶阳性、线粒体胸苷激酶阳性的人胚胎肺细胞;它们大多含有小鼠染色体和一些人类染色体,包括人胞质胸苷激酶的决定因素。mK.CV(III)细胞来源于胞质胸苷激酶阴性、线粒体胸苷激酶阳性的小鼠肾细胞和胞质胸苷激酶阳性、线粒体胸苷激酶阳性的猴肾细胞;它们大多含有小鼠染色体和一些猴染色体,包括猴胞质胸苷激酶的决定因素。圆盘PAGE分析表明,人 - 小鼠和猴 - 小鼠体细胞杂种的线粒体含有小鼠特异性线粒体胸苷激酶,但不含有人类或猴特异性线粒体胸苷激酶。这些发现表明,灵长类动物的胞质和线粒体胸苷激酶基因位于不同的染色体上。

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Mitochondrial DNA of human-mouse cell hybrids.人-鼠细胞杂种的线粒体DNA
Nature. 1971 Dec 31;234(5331):560-2. doi: 10.1038/234560a0.

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