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鸡肝血红素加氧酶cDNA的克隆、测序及表达。鸟类与哺乳动物cDNA及推导蛋白的比较。

Cloning, sequencing and expression of cDNA for chick liver haem oxygenase. Comparison of avian and mammalian cDNAs and deduced proteins.

作者信息

Evans C O, Healey J F, Greene Y, Bonkovsky H L

机构信息

Department of Medicine, Emory University School of Medicine, Atlanta, GA 30322.

出版信息

Biochem J. 1991 Feb 1;273 ( Pt 3)(Pt 3):659-66. doi: 10.1042/bj2730659.

Abstract

A cDNA from a chick liver library that encodes for haem oxygenase has been cloned and sequenced. Positive clones were identified with monospecific antibodies to the purified enzyme from chick liver and a cDNA of rat haem oxygenase-1. The length of the cDNA is 1258 bases. An open reading frame of 888 bases was identified by comparison of nucleotide and amino acid sequences with those previously identified for haem oxygenase of mammalian or avian origin. The protein corresponding to this fragment of DNA is composed of 296 amino acid residues and has a molecular mass of 33,509 Da, which is similar to that previously estimated for haem oxygenase purified from chick liver. Unequivocal identification of this clone as that complementary to haem oxygenase was provided by (a) comparison of amino acid compositions and partial sequences with those previously established for the purified enzyme, (b) comparison with nucleotide and amino acid sequences for haem oxygenase from rat and human sources and (c) expression in Escherichia coli with production of high levels of mRNA, protein and haem oxygenase activity after exposure of the transfected bacteria to isopropyl beta-D-thiogalactopyranoside (IPTG). Overall, the similarity of chick haem oxygenase to rat and human haem oxygenase (nucleotides 66% and amino acids 62%) is moderately high. The region between proline-129 and alanine-157 is identical in all three enzymes, including histidine-135, which is proposed to play a key role in binding the substrate haem at the active centre of the enzyme. Northern blots also show that treatment of chicks with CdCl2, a potent inducer of haem oxygenase, results in increases in 1.65-1.70 kb mRNA, which hybridizes selectively to the full-length cDNA or to a synthetic 24-base oligonucleotide with sequence identical to that of a portion of the haem oxygenase cDNA. These results suggest that Cd-dependent induction of haem oxygenase is due to increased transcription of the gene or stabilization of its message.

摘要

已克隆并测序了来自鸡肝文库的编码血红素加氧酶的cDNA。用针对从鸡肝中纯化的该酶的单特异性抗体和大鼠血红素加氧酶-1的cDNA鉴定出阳性克隆。该cDNA的长度为1258个碱基。通过将核苷酸和氨基酸序列与先前鉴定的哺乳动物或鸟类来源的血红素加氧酶的序列进行比较,鉴定出一个888个碱基的开放阅读框。与该DNA片段相对应的蛋白质由296个氨基酸残基组成,分子量为33509Da,这与先前从鸡肝中纯化的血红素加氧酶的估计分子量相似。通过以下方式明确鉴定该克隆为与血红素加氧酶互补的克隆:(a)将氨基酸组成和部分序列与先前建立的纯化酶的序列进行比较;(b)与大鼠和人源血红素加氧酶的核苷酸和氨基酸序列进行比较;(c)在大肠杆菌中表达,转染后的细菌在暴露于异丙基β-D-硫代半乳糖苷(IPTG)后产生高水平的mRNA、蛋白质和血红素加氧酶活性。总体而言,鸡血红素加氧酶与大鼠和人血红素加氧酶的相似性(核苷酸66%,氨基酸62%)较高。脯氨酸-129和丙氨酸-157之间的区域在所有三种酶中都是相同的,包括组氨酸-135,据推测该组氨酸在酶的活性中心结合底物血红素中起关键作用。Northern印迹还显示用CdCl2(血红素加氧酶的有效诱导剂)处理鸡会导致1.65 - 1.70kb mRNA增加,该mRNA与全长cDNA或与与血红素加氧酶cDNA一部分序列相同的合成24碱基寡核苷酸选择性杂交。这些结果表明,镉依赖性诱导血红素加氧酶是由于基因转录增加或其信息的稳定化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3e9a/1149814/2a8e67f7ef8d/biochemj00166-0167-a.jpg

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