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Determination of the Capped Site Sequence of mRNA Based on the Detection of Cap-Dependent Nucleotide Addition Using an Anchor Ligation Method

机译:基于锚定连接法检测帽依赖性核苷酸加成的mRNA的上限位点序列的确定。

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The sequence analysis of the 5′ ends of cDNAs prepared using the anchor ligation method has revealed that most of the full-length cDNAs have an additional dGMP at their 5′ end that is absent in the corresponding genome sequence. Using model RNA transcripts with cap analogues possessing 7-methylguanosine and adenosine, the base of the added nucleotide has been shown to be complementary to the base of the cap analogue, suggesting that the cDNAs possessing an additional dGMP are derived from intact mRNAs with the cap structure. On the other hand, cap-free RNA did not produce cDNA with an extra dGMP. These findings suggest that we can determine whether or not the cDNA starts from the capped site sequence of mRNA based on the presence or absence of an additional dGMP at the 5′ end of the cDNA synthesized using the anchor ligation method. This approach will be useful to determine the capped site sequence of mRNA, thus, to identify transcription start sites.
机译:使用锚定连接方法制备的cDNA 5'末端的序列分析表明,大多数全长cDNA在其5'末端具有一个额外的dGMP,而相应的基因组序列中没有该dGMP。使用具有7-甲基鸟苷和腺苷的帽类似物的模型RNA转录物,已显示所添加核苷酸的碱基与帽类似物的碱基互补,这表明具有额外dGMP的cDNA来源于带有帽的完整mRNA。结构体。另一方面,无帽RNA不会产生带有额外dGMP的cDNA。这些发现表明,我们可以基于使用锚定连接方法合成的cDNA的5'端是否存在其他dGMP,来确定cDNA是否从mRNA的帽位序列开始。该方法对于确定mRNA的加帽位点序列,从而鉴定转录起始位点将是有用的。

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