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基于表达序列标签 (EST) 数据库的人类 mRNA 5'编码序列的全基因组分析。

Genome-scale analysis of human mRNA 5' coding sequences based on expressed sequence tag (EST) database.

机构信息

Center for Research in Molecular Genetics Fondazione CARISBO, Department of Histology, Embryology and Applied Biology, University of Bologna, via Belmeloro 8, 40126 Bologna, Italy.

出版信息

Genomics. 2012 Aug;100(2):125-30. doi: 10.1016/j.ygeno.2012.05.012. Epub 2012 May 31.

Abstract

The "5' end mRNA artifact" issue refers to the incorrect assignment of the first AUG codon in an mRNA, due to the incomplete determination of its 5' end sequence. We performed a systematic identification of coding regions at the 5' end of all human known mRNAs, using an automated expressed sequence tag (EST)-based approach. Following parsing of more than 7 million BLAT alignments, we found 477 human loci, out of 18,665 analyzed, in which an extension of the mRNA 5' coding region was identified. Proof-of-concept confirmation was obtained by in vitro cloning and sequencing for GNB2L1, QARS and TDP2 cDNAs, and the consequences for the functional studies of these loci are discussed. We also generated a list of 20,775 human mRNAs where the presence of an in-frame stop codon upstream of the known start codon indicates completeness of the coding sequence at 5' in the current form.

摘要

“5' 端 mRNA 假象”问题是指由于未能完全确定其 5' 端序列,导致对 mRNA 中第一个 AUG 密码子的错误分配。我们采用一种基于自动表达序列标签(EST)的方法,对所有已知人类 mRNA 的 5' 端编码区进行了系统鉴定。在对超过 700 万个 BLAT 比对进行解析后,我们在 18665 个分析的位点中发现了 477 个人类基因座,其中鉴定出了 mRNA 5' 编码区的延伸。通过对 GNB2L1、QARS 和 TDP2 cDNA 的体外克隆和测序进行了验证,讨论了这些基因座对功能研究的影响。我们还生成了一份 20775 个人类 mRNA 的清单,其中在已知起始密码子上游存在一个框内终止密码子,表明当前形式的 5' 编码序列是完整的。

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