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小鼠中丁酰辅酶A脱氢酶的遗传学与个体发生以及Bcd - 1与Dao - 1的连锁关系

Genetics and ontogeny of butyryl CoA dehydrogenase in the mouse and linkage of Bcd-1 with Dao-1.

作者信息

Seeley T L, Holmes R S

出版信息

Biochem Genet. 1981 Apr;19(3-4):333-45. doi: 10.1007/BF00504278.

Abstract

A zymogram method has been developed for fatty acyl CoA dehydrogenase and used to examine the electrophoretic properties of butyryl CoA dehydrogenase (BCD) from mouse tissues. A single form of BCD is present in extracts of liver, kidney, heart, and intestine. Ontogenetic, tissue distribution, and subcellular fractionation results are consistent with the mitochondrial origin previously reported for this enzyme. A genetic variant for BCD-1 was used to provide evidence for a locus determining the electrophoretic properties of this enzyme (designated Bcd-1), which is linked to Dao-1 (encoding D-amino acid oxidase).

摘要

已开发出一种用于检测脂肪酰辅酶A脱氢酶的酶谱法,并用于检测小鼠组织中丁酰辅酶A脱氢酶(BCD)的电泳特性。肝脏、肾脏、心脏和肠道提取物中存在单一形式的BCD。个体发育、组织分布和亚细胞分级分离结果与先前报道的该酶的线粒体起源一致。利用BCD - 1的一个遗传变体为一个决定该酶电泳特性的基因座(命名为Bcd - 1)提供证据,该基因座与Dao - 1(编码D - 氨基酸氧化酶)连锁。

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