Nagase T, Ishikawa K, Suyama M, Kikuno R, Miyajima N, Tanaka A, Kotani H, Nomura N, Ohara O
Kazusa DNA Research Institute, Kisarazu, Chiba, Japan.
DNA Res. 1998 Oct 30;5(5):277-86. doi: 10.1093/dnares/5.5.277.
In our series of projects for accumulating sequence information on the coding sequences of unidentified human genes, we have newly determined the sequences of 100 cDNA clones from a set of size-fractionated human brain cDNA libraries, and predicted the coding sequences of the corresponding genes, named KIAA0711 to KIAA0810. These cDNA clones were selected according to their coding potentials of large proteins (50 kDa and more) in vitro. The average sizes of the inserts and corresponding open reading frames were 4.3 kb and 2.6 kb (869 amino acid residues), respectively. Sequence analyses against the public databases indicated that the predicted coding sequences of 78 genes were similar to those of known genes, 64% of which (50 genes) were categorized as proteins functionally related to cell signaling/communication, cell structure/motility and nucleic acid management. As additional information concerning genes characterized in this study, the chromosomal locations of the clones were determined by using human-rodent hybrid panels and the expression profiles among 10 human tissues were examined by reverse transcription-coupled polymerase chain reaction which was substantially improved by enzyme-linked immunosorbent assay.
在我们积累未鉴定人类基因编码序列信息的一系列项目中,我们从一组大小分级的人类脑cDNA文库中新测定了100个cDNA克隆的序列,并预测了相应基因的编码序列,命名为KIAA0711至KIAA0810。这些cDNA克隆是根据它们在体外编码大蛋白(50 kDa及以上)的潜力来选择的。插入片段和相应开放阅读框的平均大小分别为4.3 kb和2.6 kb(869个氨基酸残基)。针对公共数据库的序列分析表明,78个基因的预测编码序列与已知基因的相似,其中64%(50个基因)被归类为与细胞信号传导/通讯、细胞结构/运动性和核酸管理功能相关的蛋白质。作为有关本研究中所鉴定基因的补充信息,通过使用人-啮齿动物杂交板确定了克隆的染色体位置,并通过逆转录偶联聚合酶链反应检测了10种人类组织中的表达谱,该反应通过酶联免疫吸附测定得到了显著改进。