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载脂蛋白E、C-I和C-II基因位点上新的人类基因(APOC4)的鉴定与特性分析

Identification and characterization of a new human gene (APOC4) in the apolipoprotein E, C-I, and C-II gene locus.

作者信息

Allan C M, Walker D, Segrest J P, Taylor J M

机构信息

Gladstone Institute of Cardiovascular Disease, University of California, San Francisco 94141-9100, USA.

出版信息

Genomics. 1995 Jul 20;28(2):291-300. doi: 10.1006/geno.1995.1144.

Abstract

We have identified and characterized a previously unreported human gene that is found within the apolipoprotein (apo) E/C-I/C-II gene locus. On the basis of its location and its properties, this new gene has been designated APOC4. Nucleotide sequence analysis of genomic DNA and liver cDNA clones revealed a 3.3-kb gene consisting of three exons and two introns. Its 3' terminus lies 555 bp upstream of APOC2, giving both genes the same transcriptional orientation. The promoter of the APOC4 gene lacks a typical TATA box, consistent with an apparent heterogeneity in transcription start sites. RNase protection analysis indicated relatively low apoC-IV mRNA levels in human liver, compared to apoC-II mRNA levels. The predicted apoC-IV protein sequence, comprising 127 amino acid residues, contains a putative 25-residue signal peptide and two potential amphipathic alpha-helical domains. Amino acid sequence comparisons indicate a limited homology between apoC-IV and either apoC-I or apoC-II. Since its hepatic expression and predicted protein structure are characteristic of the other genes in this cluster, we propose that the APOC4 gene is a member of the apolipoprotein gene family.

摘要

我们已经鉴定并表征了一个先前未报道的人类基因,该基因位于载脂蛋白(apo)E/C-I/C-II基因座内。基于其位置和特性,这个新基因被命名为APOC4。对基因组DNA和肝脏cDNA克隆进行核苷酸序列分析,发现一个由三个外显子和两个内含子组成的3.3kb基因。它的3'末端位于APOC2上游555bp处,两个基因具有相同的转录方向。APOC4基因的启动子缺乏典型的TATA盒,这与转录起始位点的明显异质性一致。核糖核酸酶保护分析表明,与apoC-II mRNA水平相比,人肝脏中apoC-IV mRNA水平相对较低。预测的apoC-IV蛋白序列由127个氨基酸残基组成,包含一个推定的25个残基的信号肽和两个潜在的两亲性α-螺旋结构域。氨基酸序列比较表明,apoC-IV与apoC-I或apoC-II之间的同源性有限。由于其肝脏表达和预测的蛋白质结构是该基因簇中其他基因的特征,我们认为APOC4基因是载脂蛋白基因家族的成员。

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