Frabetti Flavia, Casadei Raffaella, Lenzi Luca, Canaider Silvia, Vitale Lorenza, Facchin Federica, Carinci Paolo, Zannotti Maria, Strippoli Pierluigi
Center for Research in Molecular Genetics "Fondazione CARISBO", Department of Histology, Embryology and Applied Biology, University of Bologna, via Belmeloro 8, 40126 Bologna (BO), Italy.
Biol Direct. 2007 Nov 27;2:34. doi: 10.1186/1745-6150-2-34.
All standard methods for cDNA cloning are affected by a potential inability to effectively clone the 5' region of mRNA. The aim of this work was to estimate mRNA open reading frame (ORF) 5' region sequence completeness in the model organism Danio rerio (zebrafish).
We implemented a novel automated approach (5'_ORF_Extender) that systematically compares available expressed sequence tags (ESTs) with all the zebrafish experimentally determined mRNA sequences, identifies additional sequence stretches at 5' region and scans for the presence of all conditions needed to define a new, extended putative ORF. Our software was able to identify 285 (3.3%) mRNAs with putatively incomplete ORFs at 5' region and, in three example cases selected (selt1a, unc119.2, nppa), the extended coding region at 5' end was cloned by reverse transcription-polymerase chain reaction (RT-PCR).
The implemented method, which could also be useful for the analysis of other genomes, allowed us to describe the relevance of the "5' end mRNA artifact" problem for genomic annotation and functional genomic experiment design in zebrafish.
所有用于cDNA克隆的标准方法都可能受到无法有效克隆mRNA 5'区域的影响。本研究的目的是评估模式生物斑马鱼中mRNA开放阅读框(ORF)5'区域序列的完整性。
我们实施了一种新颖的自动化方法(5'_ORF_Extender),该方法系统地将可用的表达序列标签(EST)与所有通过实验确定的斑马鱼mRNA序列进行比较,识别5'区域的额外序列片段,并扫描定义新的、扩展的推定ORF所需的所有条件。我们的软件能够识别出285个(3.3%)在5'区域推定ORF不完整的mRNA,并且在选择的三个示例案例(selt1a、unc119.2、nppa)中,通过逆转录-聚合酶链反应(RT-PCR)克隆了5'端的扩展编码区。
所实施的方法对其他基因组分析也可能有用,它使我们能够描述“5'端mRNA假象”问题对斑马鱼基因组注释和功能基因组实验设计的相关性。