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小鼠5-氨基酮戊酸合酶cDNA的核苷酸序列及其基因在肝脏和红细胞组织中的表达。

Nucleotide sequence of mouse 5-aminolevulinic acid synthase cDNA and expression of its gene in hepatic and erythroid tissues.

作者信息

Schoenhaut D S, Curtis P J

出版信息

Gene. 1986;48(1):55-63. doi: 10.1016/0378-1119(86)90351-3.

Abstract

The cDNA coding for 5-aminolevulinic acid (ALA) synthase (EC 2.3.1.37) in both liver and anemic spleen of the mouse has been cloned. The liver clone was selected by complementation of an Escherichia coli hemA mutant. Erythroid clones were obtained by screening a cDNA library made from mouse anemic spleen RNA, using the liver cDNA as a probe. The sequences of the spleen-derived and liver-derived cDNAs are identical. The nucleotide sequence and predicted amino acid (aa) sequence of a 1.85-kb spleen-derived cDNA is presented. The mouse ALA synthase as sequence displays extensive homology to ALA synthase of chick embryonic liver. The ALA synthase mRNA, detected by Northern blot analysis, was the same size, approx. 2.3 kb, in mouse liver, anemic spleen, and mouse erythroleukemia cells. It is therefore unlikely that different isozymic forms of ALA synthase are present in mouse erythroid and hepatic tissue and this is not the basis for the different effects of heme and porphyrinogenic compounds on the expression of liver and erythroid ALA synthase.

摘要

已克隆出小鼠肝脏和贫血脾脏中编码5-氨基乙酰丙酸(ALA)合酶(EC 2.3.1.37)的cDNA。肝脏克隆是通过对大肠杆菌hemA突变体进行互补筛选得到的。通过用肝脏cDNA作为探针筛选由小鼠贫血脾脏RNA构建的cDNA文库,获得了红系克隆。脾脏来源和肝脏来源的cDNA序列相同。给出了一个1.85 kb脾脏来源cDNA的核苷酸序列和预测的氨基酸(aa)序列。小鼠ALA合酶序列与鸡胚肝脏的ALA合酶显示出广泛的同源性。通过Northern印迹分析检测到的ALA合酶mRNA大小相同,约为2.3 kb,存在于小鼠肝脏、贫血脾脏和小鼠红白血病细胞中。因此,小鼠红系和肝组织中不太可能存在不同的ALA合酶同工型,这不是血红素和卟啉生成化合物对肝脏和红系ALA合酶表达产生不同影响的基础。

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