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人类肠道载脂蛋白B mRNA中一个新的框内翻译终止密码子的鉴定。

Identification of a novel in-frame translational stop codon in human intestine apoB mRNA.

作者信息

Hospattankar A V, Higuchi K, Law S W, Meglin N, Brewer H B

机构信息

Molecular Disease Branch, National Heart, Lung, and Blood Institute, Bethesda, MD 20892.

出版信息

Biochem Biophys Res Commun. 1987 Oct 14;148(1):279-85. doi: 10.1016/0006-291x(87)91107-7.

DOI:10.1016/0006-291x(87)91107-7
PMID:2445342
Abstract

Human apolipoprotein (apo) B exists in plasma as two isoproteins designated apoB-100 and apoB-48. ApoB-100 (512 kDa) and apoB-48 (250 kDa) are synthesized by the liver and intestine respectively. Analysis of apoB cDNA clones isolated from a human intestinal cDNA library revealed that the intestinal apoB mRNA contains a new in-frame translational stop codon. This premature stop codon is generated by a single base substitution of a 'C' to 'T' at nucleotide 6538 which converts the codon 'CAA' coding for the amino acid glutamine residue 2153 to an in-frame stop codon 'TAA'. The generation of a stop codon in the intestinal apoB mRNA appears to be tissue specific since it has not been reported in cDNA clones isolated from human liver cDNA libraries which code for the 4536 amino acid apoB-100. A potential polyadenylation signal sequence 'AATAAA' was also identified 390 bases downstream from the new stop codon. The new stop codon in the human intestinal apoB mRNA provides a potential mechanism for the biosynthesis of intestinal apoB-48.

摘要

人载脂蛋白(apo)B在血浆中以两种同功蛋白形式存在,分别称为apoB - 100和apoB - 48。apoB - 100(512 kDa)和apoB - 48(250 kDa)分别由肝脏和肠道合成。对从人肠道cDNA文库中分离出的apoB cDNA克隆进行分析发现,肠道apoB mRNA含有一个新的框内翻译终止密码子。这个提前出现的终止密码子是由核苷酸6538处的一个碱基“C”替换为“T”产生的,它将编码谷氨酰胺残基2153的密码子“CAA”转换为一个框内终止密码子“TAA”。肠道apoB mRNA中终止密码子的产生似乎具有组织特异性,因为在从人肝脏cDNA文库中分离出的编码4536个氨基酸的apoB - 100的cDNA克隆中尚未有相关报道。在新的终止密码子下游390个碱基处还鉴定出一个潜在的聚腺苷酸化信号序列“AATAAA”。人肠道apoB mRNA中的新终止密码子为肠道apoB - 48的生物合成提供了一种潜在机制。

相似文献

1
Identification of a novel in-frame translational stop codon in human intestine apoB mRNA.人类肠道载脂蛋白B mRNA中一个新的框内翻译终止密码子的鉴定。
Biochem Biophys Res Commun. 1987 Oct 14;148(1):279-85. doi: 10.1016/0006-291x(87)91107-7.
2
Human apolipoprotein B (apoB) mRNA: identification of two distinct apoB mRNAs, an mRNA with the apoB-100 sequence and an apoB mRNA containing a premature in-frame translational stop codon, in both liver and intestine.人类载脂蛋白B(apoB)信使核糖核酸(mRNA):在肝脏和肠道中均鉴定出两种不同的apoB mRNA,一种具有apoB - 100序列的mRNA,以及一种含有框内过早翻译终止密码子的apoB mRNA。
Proc Natl Acad Sci U S A. 1988 Mar;85(6):1772-6. doi: 10.1073/pnas.85.6.1772.
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Single base substitution between human intestinal and hepatic apolipoprotein B mRNA detected by ribonuclease cleavage analysis.通过核糖核酸酶切割分析检测到的人肠道和肝脏载脂蛋白B信使核糖核酸之间的单碱基取代
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Expression of apolipoprotein B mRNAs encoding higher- and lower-molecular weight isoproteins in rat liver and intestine.大鼠肝脏和肠道中编码高分子量和低分子量同工蛋白的载脂蛋白B信使核糖核酸的表达
Proc Natl Acad Sci U S A. 1989 Jan;86(2):500-4. doi: 10.1073/pnas.86.2.500.
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Apolipoprotein B mRNA editing in 12 different mammalian species: hepatic expression is reflected in low concentrations of apoB-containing plasma lipoproteins.12种不同哺乳动物物种中的载脂蛋白B信使核糖核酸编辑:肝脏表达反映在含载脂蛋白B的血浆脂蛋白低浓度中。
J Lipid Res. 1993 Aug;34(8):1367-83.
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Apolipoprotein B-48 is the product of a messenger RNA with an organ-specific in-frame stop codon.载脂蛋白B-48是一种信使核糖核酸的产物,该信使核糖核酸带有一个器官特异性的框内终止密码子。
Science. 1987 Oct 16;238(4825):363-6. doi: 10.1126/science.3659919.
7
Transgenic mice expressing full-length human apolipoprotein B-100. Full-length human apolipoprotein B mRNA is essentially not edited in mouse intestine or liver.表达全长人载脂蛋白B - 100的转基因小鼠。全长人载脂蛋白B信使核糖核酸在小鼠肠道或肝脏中基本不发生编辑。
J Biol Chem. 1992 Oct 25;267(30):21412-20.
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Apolipoprotein B48 RNA editing in chimeric apolipoprotein EB mRNA.嵌合载脂蛋白EB mRNA中的载脂蛋白B48 RNA编辑
J Biol Chem. 1989 Sep 15;264(26):15701-8.
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Thyroid hormone modulates the introduction of a stop codon in rat liver apolipoprotein B messenger RNA.甲状腺激素调节大鼠肝脏载脂蛋白B信使核糖核酸中一个终止密码子的引入。
J Biol Chem. 1988 Sep 25;263(27):13482-5.
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Evolution of intestinal apolipoprotein B mRNA editing. Chicken apolipoprotein B mRNA is not edited, but chicken enterocytes contain in vitro editing enhancement factor(s).肠道载脂蛋白B信使核糖核酸编辑的演变。鸡的载脂蛋白B信使核糖核酸不被编辑,但鸡的肠细胞含有体外编辑增强因子。
J Biol Chem. 1992 Oct 15;267(29):21265-72.

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Gut. 1989 Nov;30 Spec No(Spec No):35-43. doi: 10.1136/gut.30.spec_no.35.
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Characterization of single base substitutions in edited apolipoprotein B transcripts.编辑后的载脂蛋白B转录本中单碱基替换的特征分析。
Nucleic Acids Res. 1989 Jan 25;17(2):691-8. doi: 10.1093/nar/17.2.691.
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