首页> 外文期刊>DNA research: an international journal for rapid publication of reports on genes and genomes >Prediction of the Coding Sequences of Unidentified Human Genes. XXII. The Complete Sequences of 50 New cDNA Clones Which Code for Large Proteins
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Prediction of the Coding Sequences of Unidentified Human Genes. XXII. The Complete Sequences of 50 New cDNA Clones Which Code for Large Proteins

机译:未知人类基因编码序列的预测。二十二。 50个编码大蛋白的新cDNA克隆的完整序列

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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–IAA1988. 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 ofthese predicted gene products (81%) were classified into proteins relating to cell signaling/communication, nucleic acid management, and cell structure/motility. The expression profiles ofthe 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.
机译:作为人类cDNA项目的扩展,其目的是在未知基因的编码序列上积累序列信息,在此,我们介绍了50个cDNA克隆的完整序列,称为KIAA1939–IAA1988。在测序之前,根据其蛋白质编码潜力,通过两种方法选择要完全测序的cDNA克隆:选择10个cDNA克隆,因为它们的编码蛋白在体外转录/翻译系统中的分子量大于50 kDa;之所以选择其余的40个cDNA克隆,是因为它们的推定蛋白质(大于使用GENSCAN基因预测程序通过分析两个cDNA的两个末端序列侧翼的基因组序列确定)大于400个氨基酸残基。根据序列数据,此处分析的cDNA克隆的插入片段的平均大小和相应的开放阅读框分别为4.6 kb和1.9 kb(643个氨基酸残基)。根据对公共数据库进行同源性和基序搜索的结果,可以分配31种预测基因产物的功能类别。这些预测的基因产物中有25种(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。还通过逆转录偶联聚合酶链反应研究了该基因在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,并通过酶联免疫吸附法对其产物进行了定量。

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