Olivero Christiane E, Martínez-Terroba Elena, Zimmer Joshua, Liao Clara, Tesfaye Ephrath, Hooshdaran Nima, Schofield Jeremy A, Bendor Jordan, Fang Dorthy, Simon Matthew D, Zamudio Jesse R, Dimitrova Nadya
Department of Molecular, Cellular, and Developmental Biology, Yale University, New Haven, CT 06511, USA.
Department of Molecular Biophysics and Biochemistry, Yale University, New Haven, CT 06511, USA.
Mol Cell. 2020 Feb 20;77(4):761-774.e8. doi: 10.1016/j.molcel.2019.12.014. Epub 2020 Jan 20.
The tumor suppressor p53 transcriptionally activates target genes to suppress cellular proliferation during stress. p53 has also been implicated in the repression of the proto-oncogene Myc, but the mechanism has remained unclear. Here, we identify Pvt1b, a p53-dependent isoform of the long noncoding RNA (lncRNA) Pvt1, expressed 50 kb downstream of Myc, which becomes induced by DNA damage or oncogenic signaling and accumulates near its site of transcription. We show that production of the Pvt1b RNA is necessary and sufficient to suppress Myc transcription in cis without altering the chromatin organization of the locus. Inhibition of Pvt1b increases Myc levels and transcriptional activity and promotes cellular proliferation. Furthermore, Pvt1b loss accelerates tumor growth, but not tumor progression, in an autochthonous mouse model of lung cancer. These findings demonstrate that Pvt1b acts at the intersection of the p53 and Myc transcriptional networks to reinforce the anti-proliferative activities of p53.
肿瘤抑制因子p53通过转录激活靶基因来在应激期间抑制细胞增殖。p53也与原癌基因Myc的抑制有关,但其机制仍不清楚。在这里,我们鉴定出Pvt1b,它是长链非编码RNA(lncRNA)Pvt1的一种p53依赖性异构体,在Myc下游50 kb处表达,可被DNA损伤或致癌信号诱导,并在其转录位点附近积累。我们表明,Pvt1b RNA的产生对于顺式抑制Myc转录是必要且充分的,而不会改变该基因座的染色质组织。抑制Pvt1b会增加Myc水平和转录活性,并促进细胞增殖。此外,在肺癌的原位小鼠模型中,Pvt1b缺失会加速肿瘤生长,但不会加速肿瘤进展。这些发现表明,Pvt1b在p53和Myc转录网络的交叉点起作用,以增强p53的抗增殖活性。