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未鉴定的人类基因编码序列的预测。十二。来自大脑的100个新的cDNA克隆的完整序列,这些克隆在体外编码大蛋白。

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

作者信息

Nagase T, Ishikawa K, Suyama M, Kikuno R, Hirosawa M, Miyajima N, Tanaka A, Kotani H, Nomura N, Ohara O

机构信息

Kazusa DNA Research Institute, Kisarazu, Chiba, Japan.

出版信息

DNA Res. 1998 Dec 31;5(6):355-64. doi: 10.1093/dnares/5.6.355.

Abstract

In this paper, we report the sequences of 100 cDNA clones newly determined from a set of size-fractionated human brain cDNA libraries and predict the coding sequences of the corresponding genes, named KIAA0819 to KIAA0918. These cDNA clones were selected on the basis of their coding potentials of large proteins (50 kDa and more) by using in vitro transcription/translation assays. The sequence data showed that the average sizes of the inserts and corresponding open reading frames are 4.4 kb and 2.5 kb (831 amino acid residues), respectively. Homology and motif/domain searches against the public databases indicated that the predicted coding sequences of 83 genes were similar to those of known genes, 59% of which (49 genes) were categorized as coding for proteins functionally related to cell signaling/communication, cell structure/motility and nucleic acid management. The chromosomal locations and the expression profiles of all the genes were also examined. For 54 clones including brain-specific ones, the mRNA levels were further examined among 8 brain regions (amygdala, corpus callosum, cerebellum, caudate nucleus, hippocampus, substantia nigra, subthalamic nucleus, and thalamus), spinal cord, and fetal brain.

摘要

在本文中,我们报告了从一组大小分级的人脑cDNA文库中新测定的100个cDNA克隆的序列,并预测了相应基因(命名为KIAA0819至KIAA0918)的编码序列。这些cDNA克隆是通过体外转录/翻译分析,根据其编码大蛋白(50 kDa及以上)的潜力选择的。序列数据表明,插入片段和相应开放阅读框的平均大小分别为4.4 kb和2.5 kb(831个氨基酸残基)。针对公共数据库的同源性以及基序/结构域搜索表明,83个基因的预测编码序列与已知基因的序列相似,其中59%(49个基因)被归类为编码与细胞信号传导/通讯、细胞结构/运动性和核酸管理功能相关的蛋白质。还研究了所有基因的染色体定位和表达谱。对于包括脑特异性克隆在内的54个克隆,在8个脑区(杏仁核、胼胝体、小脑、尾状核、海马、黑质、丘脑底核和丘脑)、脊髓和胎儿脑中进一步检测了mRNA水平。

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