Fondazione Istituto FIRC di Oncologia Molecolare, at IFOM-IEO Campus Via Adamello 16, 20139 Milan, Italy.
Mol Cell. 2012 Mar 30;45(6):710-8. doi: 10.1016/j.molcel.2012.03.001.
DNA and RNA polymerases clash along the genome as they compete for the same DNA template. Cells have evolved specialized strategies to prevent and resolve replication and transcription interference. Here, we review the topology and architecture at sites of replication fork clashes with transcription bubbles as well as the regulatory circuits that control replication fork passage across transcribed genes. In the case of RNA polymerase II-transcribed genes, cotranscriptional processes such as mRNA maturation, splicing, and export influence the integrity of replication forks and transcribed loci. Fork passage likely contributes to reset the epigenetic landscape, influencing gene expression and transcriptional memory. When any of these processes are not properly coordinated, aberrant outcomes such as fork reversal and R-loop formation arise and trigger unscheduled recombinogenic events and genome rearrangements. The evolutionary implications of such conflicts on genome dynamics and their potential impact on oncogenic stress are discussed.
DNA 和 RNA 聚合酶在竞争同一 DNA 模板时沿着基因组发生冲突。细胞已经进化出专门的策略来防止和解决复制和转录干扰。在这里,我们回顾了复制叉与转录泡发生冲突的位点的拓扑结构和架构,以及控制转录基因上复制叉通过的调节回路。在 RNA 聚合酶 II 转录的基因的情况下,共转录过程,如 mRNA 成熟、剪接和输出,影响复制叉和转录基因座的完整性。叉通过可能有助于重置表观遗传景观,影响基因表达和转录记忆。当这些过程中的任何一个不能很好地协调时,就会出现异常结果,如叉反转和 R 环形成,并引发非计划的重组事件和基因组重排。讨论了这些冲突对基因组动态的进化意义及其对致癌应激的潜在影响。