Prediction of the coding sequences of unidentified human genes. XX. The complete sequences of 100 new cDNA clones from brain which code for large proteins in vitro.

T. Nagase, Manabu Nakayama, D. Nakajima, R. Kikuno, Osamu Ohara
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引用次数: 153

Abstract

To accumulate information on the coding sequences of unidentified genes, we have carried out a sequencing project of human cDNA clones which encode large proteins. We herein present the entire sequences of 100 cDNA clones of unidentified human genes, named KIAA1776 and KIAA1780-KIAA1878, from size-fractionated cDNA libraries derived from human fetal brain, adult whole brain, hippocampus and amygdala. Most of the cDNA clones to be entirely sequenced were selected as cDNAs which were shown to have coding potentiality by in vitro transcription/translation experiments, and some clones were chosen by using computer-assisted analysis of terminal sequences of cDNAs. Three of these clones (fibrillin2/KIAA1776, MEGF10/KIAA1780 and MEGF11/KIAA1781) were isolated as genes encoding proteins with multiple EGF-like domains by motif-trap screening. The average sizes of the inserts and corresponding open reading frames of eDNA clones analyzed here reached 4.7 kb and 2.4 kb (785 amino acid residues), respectively. From the results of homology and motif searches against the public databases, the functional categories of the predicted gene products of 54 genes were determined; 93% of these predicted gene products (50 gene products) were classified as proteins related to cell signaling/communication, nucleic acid management, or cell structure/motility. To collect additional information on these genes, their expression profiles were also studied in 10 human tissues, 8 brain regions, spinal cord, fetal brain and fetal liver by reverse transcription-coupled polymerase chain reaction, products of which were quantified by enzyme-linked immunosorbent assay.
未知人类基因编码序列的预测。XX。100个新的大脑cDNA克隆的完整序列,这些克隆在体外编码大蛋白。
为了积累未知基因的编码序列信息,我们开展了编码大蛋白的人类cDNA克隆测序项目。在此,我们从人类胎儿脑、成人全脑、海马和杏仁核的cDNA文库中提取了100个未知人类基因的cDNA克隆,命名为KIAA1776和KIAA1780-KIAA1878。大部分待完全测序的cDNA克隆是通过体外转录/翻译实验证明具有编码潜力的cDNA,一些克隆是通过计算机辅助分析cDNA末端序列选择的。其中三个克隆(fibrin2 /KIAA1776, MEGF10/KIAA1780和MEGF11/KIAA1781)通过基序陷阱筛选分离到编码多个egf样结构域蛋白的基因。本文分析的eDNA克隆的插入片段和相应的开放阅读框的平均大小分别为4.7 kb和2.4 kb(785个氨基酸残基)。通过对公共数据库的同源性和基序搜索,确定了54个基因的预测基因产物的功能类别;这些预测的基因产物(50个基因产物)中有93%被归类为与细胞信号/通讯、核酸管理或细胞结构/运动相关的蛋白质。为了收集这些基因的更多信息,我们还利用逆转录偶联聚合酶链反应研究了这些基因在10个人体组织、8个脑区、脊髓、胎儿脑和胎儿肝脏中的表达谱,并用酶联免疫吸附法对其产物进行了定量分析。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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