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来自神经母细胞瘤细胞的视黄酸调节的类unc-33磷蛋白基因(hUlip)人类同源物的鉴定与表征

Identification and characterization of a retinoic acid-regulated human homologue of the unc-33-like phosphoprotein gene (hUlip) from neuroblastoma cells.

作者信息

Gaetano C, Matsuo T, Thiele C J

机构信息

Cell and Molecular Biology Section, Pediatric Oncology Branch, NCI, National Institutes of Health, Bethesda, Maryland 20892, USA.

出版信息

J Biol Chem. 1997 May 2;272(18):12195-201. doi: 10.1074/jbc.272.18.12195.

DOI:10.1074/jbc.272.18.12195
PMID:9115293
Abstract

A cDNA, 7G1, was isolated from retinoic acid (RA) differentiated neuroblastoma cells whose expression was high in human fetal brain and spinal cord mRNA but undetectable in adult brain or non-neuronal tissues. Sequence analysis indicates that 7G1 is homologous to the Caenorhabditis elegans gene unc-33. A 5.5-kilobase pair full-length cDNA from a human fetal brain cDNA library contains an 1710-base pair open reading frame. Because the predicted 570 amino acid sequence of 7G1 shares 98% identity with the murine Ulip gene product, an unc-33-like-phosphoprotein, we refer to 7G1 as the human Ulip (hUlip). hUlip is also similar to the bacterial enzyme D-hydantoinase and the recently described vertebrate gene products CRMP62, TOAD-64, CRMP1, CRMP2, and mUNC. RA stimulates an increase in hUlip mRNA that is transcriptionally regulated. RA stimulates an increase in polypeptides of 58, 60, 65, and 70 kDa with the 58- and 65-kDa species being dephosphorylated forms of the 60- and 70-kDa species. This study presents a model in which to study the regulation and expression of the hUlip gene, a member of an emerging family of molecules that potentially mediates signals involved in axonal outgrowth.

摘要

从视黄酸(RA)分化的神经母细胞瘤细胞中分离出一种名为7G1的cDNA,其在人胎脑和脊髓mRNA中的表达较高,但在成体脑或非神经组织中检测不到。序列分析表明,7G1与秀丽隐杆线虫基因unc-33同源。来自人胎脑cDNA文库的一个5.5千碱基对的全长cDNA包含一个1710碱基对的开放阅读框。由于预测的7G1的570个氨基酸序列与鼠类Ulip基因产物(一种unc-33样磷蛋白)具有98%的同一性,我们将7G1称为人Ulip(hUlip)。hUlip也类似于细菌酶D-海因酶以及最近描述的脊椎动物基因产物CRMP62、TOAD-64、CRMP1、CRMP2和mUNC。RA刺激hUlip mRNA的增加,这是由转录调控的。RA刺激58、60、65和70 kDa多肽的增加,其中58 kDa和65 kDa的物种是60 kDa和70 kDa物种的去磷酸化形式。本研究提出了一个模型,用于研究hUlip基因的调控和表达,hUlip基因是一个新兴分子家族的成员,可能介导参与轴突生长的信号。

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