Prediction of the coding sequences of unidentified human genes. XXII. The complete sequences of 50 new cDNA clones which code for large proteins.

T. Nagase, R. Kikuno, O. Ohara
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引用次数: 50

Abstract

As an extension of human cDNA projects for accumulating sequence information on the coding sequences of unidentified genes, we herein present the entire sequences of 50 cDNA clones, named KIAA1939-KIAA1988. cDNA clones to be entirely sequenced were selected by two approaches based on their protein-coding potentialities prior to sequencing: 10 cDNA clones were chosen because their encoding proteins had a molecular mass larger than 50 kDa in an in vitro transcription/translation system; the remaining 40 cDNA clones were selected because their putative proteins-as determined by analysis of the genomic sequences flanked by both the terminal sequences of cDNAs using the GENSCAN gene prediction program-were larger than 400 amino acid residues. According to the sequence data, the average sizes of the inserts and corresponding open reading frames of cDNA clones analyzed here were 4.6 kb and 1.9 kb (643 amino acid residues), respectively. From the results of homology and motif searches against the public databases, the functional categories of the 31 predicted gene products could be assigned; 25 of these predicted gene products (81%) were classified into proteins relating to cell signaling/communication, nucleic acid management, and cell structure/motility. The expression profiles of the genes were also studied in 10 human tissues, 8 brain regions, spinal cord, fetal brain and fetal liver by reverse transcription-coupled polymerase chain reaction, the products of which were quantified by enzyme-linked immunosorbent assay.
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未知人类基因编码序列的预测。第二十二。50个新的编码大蛋白质的cDNA克隆的完整序列。
作为人类cDNA项目的延伸,为了积累未知基因编码序列的序列信息,我们在此提出了50个cDNA克隆的完整序列,命名为KIAA1939-KIAA1988。在测序之前,根据蛋白质编码潜力,通过两种方法选择需要完全测序的cDNA克隆:选择10个cDNA克隆,因为它们的编码蛋白在体外转录/翻译系统中分子量大于50 kDa;剩下的40个cDNA克隆之所以被选择,是因为它们假定的蛋白质——通过使用GENSCAN基因预测程序对cDNA末端序列两侧的基因组序列进行分析确定——大于400个氨基酸残基。根据序列数据,本文分析的cDNA克隆的插入片段和相应的开放阅读框的平均大小分别为4.6 kb和1.9 kb(643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31个预测基因产物的功能类别;在这些预测的基因产物中,有25个(81%)被分类为与细胞信号/通讯、核酸管理和细胞结构/运动有关的蛋白质。通过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、胎脑和胎肝中的表达谱,并采用酶联免疫吸附法对产物进行了定量分析。
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