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编码大鼠肾脏S-腺苷甲硫氨酸合成酶的cDNA的分子克隆及核苷酸序列

Molecular cloning and nucleotide sequence of cDNA encoding the rat kidney S-adenosylmethionine synthetase.

作者信息

Horikawa S, Sasuga J, Shimizu K, Ozasa H, Tsukada K

机构信息

Department of Pathological Biochemistry, Tokyo Medical and Dental University, Japan.

出版信息

J Biol Chem. 1990 Aug 15;265(23):13683-6.

PMID:1696256
Abstract

We previously reported the isolation of a cDNA encoding the liver-specific isozyme of rat S-adenosylmethionine synthetase from a lambda gt11 rat liver cDNA library. Using this cDNA as a probe, we have isolated and sequenced cDNA clones for the rat kidney S-adenosylmethionine synthetase (extrahepatic isoenzyme) from a lambda gt11 rat kidney cDNA library. The complete coding sequence of this enzyme mRNA was obtained from two overlapping cDNA clones. The amino acid sequence deduced from the cDNAs indicates that this enzyme contains 395 amino acids and has a molecular mass of 43,715 Da. The predicted amino acid sequence of this protein shares 85% similarity with that of rat liver S-adenosylmethionine synthetase. This result suggests that kidney and liver isoenzymes may have originated from a common ancestral gene. In addition, comparison of known S-adenosylmethionine synthetase sequences among different species also shows that these proteins have a high degree of similarity. The distribution of kidney- and liver-type S-adenosylmethionine synthetase mRNAs in kidney, liver, brain, and testis were examined by RNA blot hybridization analysis with probes specific for the respective mRNAs. A 3.4-kilobase (kb) mRNA species hybridizable with a probe for kidney S-adenosylmethionine synthetase was found in all tissues examined except for liver, while a 3.4-kb mRNA species hybridizable with a probe for liver S-adenosylmethionine synthetase was only present in the liver. The 3.4-kb kidney-type isozyme mRNA showed the same molecular size as the liver-type isozyme mRNA. Thus, kidney- and liver-type S-adenosylmethionine synthetase isozyme mRNAs were expressed in various tissues with different tissue specificities.

摘要

我们之前报道了从λgt11大鼠肝脏cDNA文库中分离出编码大鼠S-腺苷甲硫氨酸合成酶肝脏特异性同工酶的cDNA。利用该cDNA作为探针,我们从λgt11大鼠肾脏cDNA文库中分离并测序了大鼠肾脏S-腺苷甲硫氨酸合成酶(肝外同工酶)的cDNA克隆。该酶mRNA的完整编码序列是从两个重叠的cDNA克隆中获得的。从cDNA推导的氨基酸序列表明该酶含有395个氨基酸,分子量为43715道尔顿。该蛋白质预测的氨基酸序列与大鼠肝脏S-腺苷甲硫氨酸合成酶的氨基酸序列具有85%的相似性。这一结果表明肾脏和肝脏同工酶可能起源于一个共同的祖先基因。此外,不同物种间已知的S-腺苷甲硫氨酸合成酶序列比较也表明这些蛋白质具有高度的相似性。通过用各自mRNA特异性探针进行RNA印迹杂交分析,检测了肾脏型和肝脏型S-腺苷甲硫氨酸合成酶mRNA在肾脏、肝脏、大脑和睾丸中的分布。在除肝脏外的所有检测组织中都发现了一种可与肾脏S-腺苷甲硫氨酸合成酶探针杂交的3.4千碱基(kb)mRNA,而一种可与肝脏S-腺苷甲硫氨酸合成酶探针杂交的3.4-kb mRNA仅存在于肝脏中。3.4-kb肾脏型同工酶mRNA与肝脏型同工酶mRNA的分子大小相同。因此,肾脏型和肝脏型S-腺苷甲硫氨酸合成酶同工酶mRNA在不同组织中以不同的组织特异性表达。

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