Sridhara Sreerama Chaitanya, Carvalho Sílvia, Grosso Ana Rita, Gallego-Paez Lina Marcela, Carmo-Fonseca Maria, de Almeida Sérgio Fernandes
Instituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa, 1600-276 Lisboa, Portugal.
Instituto de Medicina Molecular, Faculdade de Medicina, Universidade de Lisboa, 1600-276 Lisboa, Portugal.
Cell Rep. 2017 Jan 10;18(2):334-343. doi: 10.1016/j.celrep.2016.12.050.
Genomic instability is frequently caused by nucleic acid structures termed R-loops that are formed during transcription. Despite their harmful potential, mechanisms that sense, signal, and suppress these structures remain elusive. Here, we report that oscillations in transcription dynamics are a major sensor of R-loops. We show that pausing of RNA polymerase II (RNA Pol II) initiates a signaling cascade whereby the serine/arginine protein kinase 2 (SRPK2) phosphorylates the DDX23 helicase, culminating in the suppression of R-loops. We show that in the absence of either SRPK2 or DDX23, accumulation of R-loops leads to massive genomic instability revealed by high levels of DNA double-strand breaks (DSBs). Importantly, we found DDX23 mutations in several cancers and detected homozygous deletions of the entire DDX23 locus in 10 (17%) adenoid cystic carcinoma (ACC) samples. Our results unravel molecular details of a link between transcription dynamics and RNA-mediated genomic instability that may play important roles in cancer development.
基因组不稳定常常由转录过程中形成的名为R环的核酸结构所导致。尽管它们具有潜在危害,但感知、发出信号并抑制这些结构的机制仍不清楚。在此,我们报告转录动力学的振荡是R环的主要传感器。我们表明,RNA聚合酶II(RNA Pol II)的暂停启动了一个信号级联反应,丝氨酸/精氨酸蛋白激酶2(SRPK2)使DDX23解旋酶磷酸化,最终抑制R环。我们表明,在缺乏SRPK2或DDX23的情况下,R环的积累会导致高水平DNA双链断裂(DSB)所揭示的大规模基因组不稳定。重要的是,我们在几种癌症中发现了DDX23突变,并在10个(17%)腺样囊性癌(ACC)样本中检测到整个DDX23基因座的纯合缺失。我们的结果揭示了转录动力学与RNA介导的基因组不稳定之间联系的分子细节,这可能在癌症发展中发挥重要作用。