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Characterization of cDNA clones selected by the GeneMark analysis from size-fractionated cDNA libraries from human brain.

机译:从人脑中尺寸分馏的CDNA文库中基因克分析选择的cDNA克隆的表征。

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We have conducted a sequencing project of human cDNAs which encode large proteins in brain. For selection of cDNA clones to be sequenced in this project, cDNA clones have been experimentally examined by in vitro transcription/translation prior to sequencing. In this study, we tested an alternative approach for picking up cDNA clones having a high probability of carrying protein coding region. This approach exploited 5'-end single-pass sequence data and the GeneMark program for assessing protein-coding potential, and allowed us to select 74 clones out of 14,804 redundant cDNA clones. The complete sequence data of these 74 clones revealed that 45% of them encoded proteins consisting of more than 500 amino acid residues while all the clones thus selected carried possible protein coding sequences as expected. The results indicated that the GeneMark analysis of 5'-end sequences of cDNAs offered us a simple and effective means to select cDNA clones with protein-coding potential although the sizes of the encoded proteins could not be predicted.
机译:我们已经进行了人类CDNA的测序项目,其在大脑中编码大蛋白质。为了在该项目中选择要测序的cDNA克隆,已经通过在测序之前通过体外转录/翻译进行了实验检查cDNA克隆。在该研究中,我们测试了一种替代方法,用于拾取具有携带蛋白质编码区域的高概率的cDNA克隆。该方法利用5'-End单通序列数据和用于评估蛋白质编码潜力的基因态程序,并使我们选择14,804个冗余cDNA克隆中的74个克隆。这些74个克隆的完整序列数据显示,它们中的45%编码由500多个氨基酸残基组成的蛋白质,而这些克隆如所选择的所有克隆所选择的蛋白质编码序列。结果表明,CDNA的5'-结束序列的基因克分析提供了一种简单有效的方法,以选择具有蛋白质编码电位的cDNA克隆,尽管无法预测编码蛋白的尺寸。

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