Department of Chemistry and Biochemistry, The City College of New York, New York, New York 10031, USA.
Biochemistry and Chemistry Ph.D. Programs, The City University of New York Graduate Center, New York, New York 10016, USA.
RNA. 2022 Oct;28(10):1315-1324. doi: 10.1261/rna.078981.121. Epub 2022 Jul 19.
Circularized single-stranded DNA oligonucleotides, or coligos, show promise as promoter-independent RNA polymerase III (Pol III) transcription templates for generating small RNA in human cells. Using a modified small RNA-seq method, we studied the sequence and secondary structure characteristics that determine Pol III initiation and termination on six coligo templates. The coligos each consisted of an imperfectly base-paired stem flanked by one larger and one smaller loop and were unrelated in sequence. Small RNA-seq data from Pol III coligo transcripts revealed a strong preference for initiating transcription within a 5-nucleotide (nt) window spanning the stem-larger loop junction (loop size 11-24 nt). Transcription in all cases proceeded into the stem rather than into the larger loop, indicating the junction is a site-specific, secondary structure-based Pol III transcription initiator. On average, 81% of sequencing reads showed initiation within this 5 nt junction region, with a template start site nucleotide preference of C > T >> A > G, and a requirement for a template purine at Tss-1. Termination was less precise than initiation and occurred in the larger loop at the same end of the stem where transcription initiated. Termination efficiency was on average 82% and was distributed among the first 11 single-stranded larger loop nt following the stem. The size heterogeneity of Pol III coligo transcripts is thus mainly due to 3' end heterogeneity, whereas the RNA 5' ends were more predictable and homogeneous. Transcription termination did not require an oligo dA template sequence, indicating that termination in this context may be mechanistically different than Pol III's normal gene-context termination. A stepwise model for coligo transcription by Pol III is proposed.
环形单链 DNA 寡核苷酸,或 coligos,作为 RNA 聚合酶 III(Pol III)启动子独立转录模板,在人类细胞中产生小 RNA 具有很大的应用潜力。我们使用改良的小 RNA-seq 方法,研究了决定 Pol III 在六个 coligo 模板上起始和终止的序列和二级结构特征。这些 coligos 每个都由一个不完全碱基配对的茎侧翼连接一个较大的环和一个较小的环组成,序列上彼此没有关联。Pol III coligo 转录物的小 RNA-seq 数据显示,在跨越茎-大环连接(环大小为 11-24 个核苷酸)的 5 个核苷酸(nt)窗口内起始转录的强烈偏好。在所有情况下,转录都进入茎内而不是进入大环,表明该连接是一个基于特定二级结构的 Pol III 转录起始子。平均而言,81%的测序reads 显示在这个 5 nt 连接区域内起始,模板起始位点核苷酸偏好为 C>T>>A>G,并且需要 Tss-1 处的模板嘌呤。终止不如起始精确,并且在与转录起始相同的茎的大环末端发生。终止效率平均为 82%,并分布在茎后的第一个 11 个单链大环 nt 中。因此,Pol III coligo 转录物的大小异质性主要是由于 3'端异质性,而 RNA 5'端则更可预测且更均匀。终止不需要寡聚 dA 模板序列,这表明在这种情况下,终止可能在机制上与 Pol III 的正常基因环境终止不同。提出了 Pol III 转录 coligo 的逐步模型。