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克隆一种与长链脂肪酸结合或转运有关的大鼠脂肪细胞膜蛋白,该蛋白在前脂肪细胞分化过程中被诱导产生。与人类CD36具有同源性。

Cloning of a rat adipocyte membrane protein implicated in binding or transport of long-chain fatty acids that is induced during preadipocyte differentiation. Homology with human CD36.

作者信息

Abumrad N A, el-Maghrabi M R, Amri E Z, Lopez E, Grimaldi P A

机构信息

Department of Physiology and Biophysics, State University of New York, Stony Brook 11794.

出版信息

J Biol Chem. 1993 Aug 25;268(24):17665-8.

PMID:7688729
Abstract

A cDNA for an adipocyte membrane protein, implicated in the transport of long-chain fatty acids, was isolated by screening with a synthetic oligonucleotide derived from the amino terminal sequence of the protein. The 88-kDa adipocyte membrane protein was previously identified by covalent labeling with N-sulfosuccinimidyl esters of long-chain fatty acids which irreversibly inhibited fatty acid transport by 75% (Harmon, C. M., and Abumrad, N.A. (1993) J. Membr. Biol. 124, 261-268). The cDNA (FAT, 2432 base pairs (bp)) contained 70 bp of 5'-untranslated sequence, an open reading frame encoding a 472-amino acid protein with a predicted molecular mass of 52466, and 940 bp of 3'-untranslated sequence with two polyadenylation signal sequences but with no polyadenylation tail. The deduced protein sequence predicted two transmembrane segments and 10 potential N-linked glycosylation sites. Extensive glycosylation most likely explains why the molecular mass of the isolated protein (88 kDa) is different from that deduced from the cDNA sequence (53 kDa). The sequence of FAT is 85% homologous with that of glycoprotein IV (CD36) identified in human platelets and in lactating mammary epithelium. Consistent with this, a polyclonal antibody against CD36 reacted with adipocyte plasma membranes and detected a single band at 88 kDa. Northern blot analysis of RNA obtained from rat adipose tissue and probed with the cDNA identified two major transcripts of 4.8 and 2.9 kilobases which were abundant in heart, intestine, fat, muscle, and testis. The mRNAs were not detectable in cultured adipose cell lines (Ob1771, 3T3F442A) at the fibroblastic stage but were strongly induced during the differentiation process and by treatment of preadipocytes with dexamethasone, conditions that were also associated with an increase in oleate transport. In contrast, the fibroblastic cell lines 3T3-C2 and L929, which do not differentiate, did not express the mRNAs at all stages of culture. The data suggest that FAT and CD36 belong to a family of proteins that bind/transport long-chain fatty acids or function as regulators of these processes.

摘要

通过用源自该蛋白质氨基末端序列的合成寡核苷酸进行筛选,分离出一种与长链脂肪酸转运有关的脂肪细胞膜蛋白的互补DNA(cDNA)。88 kDa的脂肪细胞膜蛋白先前是通过用长链脂肪酸的N-磺基琥珀酰亚胺酯进行共价标记而鉴定的,这种标记不可逆地抑制了75%的脂肪酸转运(哈蒙,C.M.,和阿布姆拉德,N.A.(1993年)《膜生物学杂志》124卷,261 - 268页)。该cDNA(FAT,2432个碱基对(bp))包含70 bp的5'-非翻译序列、一个编码472个氨基酸的蛋白质的开放阅读框,预测分子量为52466,以及940 bp的3'-非翻译序列,带有两个聚腺苷酸化信号序列但没有聚腺苷酸尾巴。推导的蛋白质序列预测有两个跨膜区段和10个潜在的N-连接糖基化位点。广泛的糖基化很可能解释了为什么分离出的蛋白质分子量(88 kDa)与从cDNA序列推导的分子量(53 kDa)不同。FAT的序列与在人血小板和泌乳乳腺上皮中鉴定出的糖蛋白IV(CD36)的序列有85%的同源性。与此一致,一种针对CD36的多克隆抗体与脂肪细胞质膜发生反应,并在88 kDa处检测到一条单一的条带。用该cDNA对从大鼠脂肪组织获得的RNA进行Northern印迹分析,鉴定出4.8和2.9千碱基的两个主要转录本,它们在心脏、肠道、脂肪、肌肉和睾丸中大量存在。在成纤维细胞阶段的培养脂肪细胞系(Ob1771、3T3F442A)中未检测到这些mRNA,但在分化过程中以及用地塞米松处理前脂肪细胞时被强烈诱导,这些条件也与油酸转运增加相关。相比之下,不发生分化的成纤维细胞系3T3 - C2和L929在培养的所有阶段都不表达这些mRNA。数据表明FAT和CD36属于一类结合/转运长链脂肪酸或作为这些过程调节因子发挥作用的蛋白质家族。

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