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Mapping of transcription start sites in Saccharomyces cerevisiae using 5 ' SAGE

机译:使用5'SAGE映射酿酒酵母中的转录起始位点

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A minimally addressed area in Saccharomyces cerevisiae research is the mapping of transcription start sites (TSS). Mapping of TSS in S. cerevisiae has the potential to contribute to our understanding of gene regulation, transcription, mRNA stability and aspects of RNA biology. Here, we use 50 SAGE to map 50 TSS in S. cerevisiae. Tags identifying the first 15-17 bases of the transcripts are created, ligated to form ditags, amplified, concatemerized and ligated into a vector to create a library. Each clone sequenced from this library identifies 10-20 TSS. We have identified 13 746 unique, unambiguous sequence tags from 2231 S. cerevisiae genes. TSS identified in this study are consistent with published results, with primer extension results described here, and are consistent with expectations based on previous work on transcription initiation. We have aligned the sequence flanking 4637 TSS to identify the consensus sequence A(A(rich))(5)NPyA(A/T)NN(A(rich))(6), which confirms and expands the previous reported PyA(A/T) Pu consensus pattern. The TSS data allowed the identification of a previously unrecognized gene, uncovered errors in previous annotation, and identified potential regulatory RNAs and upstream open reading frames in 50'-untranslated region.
机译:酿酒酵母研究中的最小寻址区域是转录起始位点(TSS)的定位。酿酒酵母中TSS的作图可能有助于我们对基因调节,转录,mRNA稳定性和RNA生物学方面的理解。在这里,我们使用50 SAGE来映射酿酒酵母中的50 TSS。创建识别转录本的前15-17个碱基的标签,将其连接形成双标签,将其扩增,连接并连接到载体中以创建一个文库。从该文库测序的每个克隆都鉴定出10-20个TSS。我们从2231啤酒酵母基因中鉴定出13 746个独特,明确的序列标签。本研究中鉴定的TSS与已发表的结果一致,引物延伸结果在此描述,并且与先前基于转录启动工作的预期一致。我们已经比对了序列4637 TSS的序列,以鉴定共有序列A(A(rich))(5)NPyA(A / T)NN(A(rich))(6),该序列确认并扩展了先前报道的PyA(A / T)Pu共识模式。 TSS数据可以识别先前无法识别的基因,先前注释中未发现的错误,并可以识别潜在的调控RNA和50'非翻译区的上游开放阅读框。

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