Department of Biochemistry, University of Oxford, Oxford, UK.
Yeast. 2024 Apr;41(4):222-241. doi: 10.1002/yea.3931. Epub 2024 Mar 3.
Genomes from yeast to humans are subject to pervasive transcription. A single round of pervasive transcription is sufficient to alter local chromatin conformation, nucleosome dynamics and gene expression, but is hard to distinguish from background signals. Size fractionated native elongating transcript sequencing (sfNET-Seq) was developed to precisely map nascent transcripts independent of expression levels. RNAPII-associated nascent transcripts are fractionation into different size ranges before library construction. When anchored to the transcription start sites (TSS) of annotated genes, the combined pattern of the output metagenes gives the expected reference pattern. Bioinformatic pattern matching to the reference pattern identified 9542 transcription units in Saccharomyces cerevisiae, of which 47% are coding and 53% are noncoding. In total, 3113 (33%) are unannotated noncoding transcription units. Anchoring all transcription units to the TSS or polyadenylation site (PAS) of annotated genes reveals distinctive architectures of linked pairs of divergent transcripts approximately 200nt apart. The Reb1 transcription factor is enriched 30nt downstream of the PAS only when an upstream (TSS -60nt with respect to PAS) noncoding transcription unit co-occurs with a downstream (TSS +150nt) coding transcription unit and acts to limit levels of upstream antisense transcripts. The potential for extensive transcriptional interference is evident from low abundance unannotated transcription units with variable TSS (median -240nt) initiating within a 500nt window upstream of, and transcribing over, the promoters of protein-coding genes. This study confirms a highly interleaved yeast genome with different types of transcription units altering the chromatin landscape in distinctive ways, with the potential to exert extensive regulatory control.
从酵母到人,基因组都受到广泛转录的影响。单次广泛转录足以改变局部染色质构象、核小体动力学和基因表达,但很难与背景信号区分开来。大小分级原生延伸转录测序(sfNET-Seq)的开发是为了在不依赖表达水平的情况下精确绘制新生转录本。在构建文库之前,将与 RNA 聚合酶 II 相关的新生转录本分成不同的大小范围。当与注释基因的转录起始位点(TSS)锚定时,输出元基因的组合模式给出了预期的参考模式。与参考模式的生物信息学模式匹配确定了酿酒酵母中的 9542 个转录单元,其中 47%是编码的,53%是非编码的。总共,3113(33%)是非注释的非编码转录单元。将所有转录单元锚定到注释基因的 TSS 或聚腺苷酸化位点(PAS)上,可以揭示出大约 200nt 分开的发散转录本之间的独特连接对结构。只有当上游(相对于 PAS 的 TSS -60nt)非编码转录单元与下游(TSS +150nt)编码转录单元共同存在时,Reb1 转录因子才会在 PAS 下游 30nt 处富集,并且起到限制上游反义转录本水平的作用。从具有可变 TSS(中位数 -240nt)的低丰度非注释转录单元中可以明显看出广泛转录干扰的可能性,这些转录单元在启动子上游 500nt 窗口内起始,并转录超过蛋白质编码基因的启动子。这项研究证实了酵母基因组具有高度交织的结构,不同类型的转录单元以独特的方式改变染色质景观,具有广泛的调节控制潜力。