Technological Advances for Genomics and Clinics (TAGC), Case 928, 163 Avenue de Luminy, 13288, Marseille cedex 09, France.
BMC Genomics. 2013 Dec 23;14:914. doi: 10.1186/1471-2164-14-914.
Divergent transcription is a wide-spread phenomenon in mammals. For instance, short bidirectional transcripts are a hallmark of active promoters, while longer transcripts can be detected antisense from active genes in conditions where the RNA degradation machinery is inhibited. Moreover, many described long non-coding RNAs (lncRNAs) are transcribed antisense from coding gene promoters. However, the general significance of divergent lncRNA/mRNA gene pair transcription is still poorly understood. Here, we used strand-specific RNA-seq with high sequencing depth to thoroughly identify antisense transcripts from coding gene promoters in primary mouse tissues.
We found that a substantial fraction of coding-gene promoters sustain divergent transcription of long non-coding RNA (lncRNA)/mRNA gene pairs. Strikingly, upstream antisense transcription is significantly associated with genes related to transcriptional regulation and development. Their promoters share several characteristics with those of transcriptional developmental genes, including very large CpG islands, high degree of conservation and epigenetic regulation in ES cells. In-depth analysis revealed a unique GC skew profile at these promoter regions, while the associated coding genes were found to have large first exons, two genomic features that might enforce bidirectional transcription. Finally, genes associated with antisense transcription harbor specific H3K79me2 epigenetic marking and RNA polymerase II enrichment profiles linked to an intensified rate of early transcriptional elongation.
We concluded that promoters of a class of transcription regulators are characterized by a specialized transcriptional control mechanism, which is directly coupled to relaxed bidirectional transcription.
在哺乳动物中,转录的分支是一种广泛存在的现象。例如,短的双向转录本是活跃启动子的标志,而在 RNA 降解机制被抑制的情况下,从活跃基因的反义方向可以检测到更长的转录本。此外,许多描述的长非编码 RNA(lncRNA)是从编码基因启动子反义转录的。然而,分支 lncRNA/mRNA 基因对转录的一般意义仍然知之甚少。在这里,我们使用具有高测序深度的链特异性 RNA-seq 来彻底鉴定初级小鼠组织中编码基因启动子的反义转录本。
我们发现,相当一部分编码基因启动子支持长非编码 RNA(lncRNA)/mRNA 基因对的分支转录。引人注目的是,上游反义转录与转录调控和发育相关的基因显著相关。它们的启动子与转录发育基因的启动子具有几个共同特征,包括非常大的 CpG 岛、ES 细胞中的高度保守性和表观遗传调控。深入分析揭示了这些启动子区域独特的 GC 倾斜模式,而相关的编码基因具有大的第一外显子,这两个基因组特征可能强制双向转录。最后,与反义转录相关的基因具有特定的 H3K79me2 表观遗传标记和 RNA 聚合酶 II 富集图谱,与早期转录延伸率的提高有关。
我们得出结论,一类转录调节剂的启动子的特征是一种特殊的转录控制机制,该机制与松弛的双向转录直接相关。