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小鼠载脂蛋白A-IV基因:核苷酸序列及高脂饮食诱导作用

Mouse apolipoprotein A-IV gene: nucleotide sequence and induction by a high-lipid diet.

作者信息

Williams S C, Bruckheimer S M, Lusis A J, LeBoeuf R C, Kinniburgh A J

出版信息

Mol Cell Biol. 1986 Nov;6(11):3807-14. doi: 10.1128/mcb.6.11.3807-3814.1986.

Abstract

Apolipoprotein A-IV (apo A-IV) functions in conjunction with other apolipoproteins to form lipoprotein particles which are involved in lipid homeostasis. In this report we present the nucleotide sequence of the mouse apo A-IV gene and demonstrate its induction in the liver by chronically high dietary lipid. The apo A-IV gene consists of three exons and two introns. The introns separate evolutionarily conserved and functional polypeptide domains. Intron 1 divides most of the apo A-IV signal peptide from the amino terminus of the mature plasma protein. The second intron separates a highly evolutionarily conserved, variant amphipathic peptide repeat from the remainder of the mature apo A-IV protein. The 5' flanking region has several interesting features. The apo A-IV gene has variant TATA and CAT box sequences, TTTAAA and CCAACG, respectively. There are five G-rich direct repeats of 10 nucleotides and a short inverted repeat in the 5' flanking region. We speculate that these sequence elements in the 5' flanking region may be involved in the regulation of apo A-IV gene expression. We also show that chronically high dietary lipid induces liver apo A-IV levels 10-fold in C57BL/6 mice, a strain susceptible to atherosclerotic lesions, while we observed no induction in nonsusceptible BALB/c and C3H mice.

摘要

载脂蛋白A-IV(apo A-IV)与其他载脂蛋白共同发挥作用,形成参与脂质稳态的脂蛋白颗粒。在本报告中,我们展示了小鼠apo A-IV基因的核苷酸序列,并证明了长期高膳食脂质可诱导其在肝脏中的表达。apo A-IV基因由三个外显子和两个内含子组成。内含子分隔了进化上保守的功能性多肽结构域。内含子1将apo A-IV信号肽的大部分与成熟血浆蛋白的氨基末端分开。第二个内含子将一个高度进化保守的可变两亲性肽重复序列与成熟apo A-IV蛋白的其余部分分开。5'侧翼区域有几个有趣的特征。apo A-IV基因分别具有变体TATA盒和CAT盒序列,即TTTAAA和CCAACG。在5'侧翼区域有五个富含G的10个核苷酸的直接重复序列和一个短的反向重复序列。我们推测5'侧翼区域中的这些序列元件可能参与apo A-IV基因表达的调控。我们还表明,长期高膳食脂质可使易患动脉粥样硬化病变的C57BL/6小鼠肝脏中的apo A-IV水平升高10倍,而在不易感的BALB/c和C3H小鼠中未观察到诱导作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a9ae/367142/ab23981563de/molcellb00095-0256-a.jpg

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