NONO regulates the intra-S-phase checkpoint in response to UV radiation

被引:28
作者
Alfano, L. [1 ]
Costa, C. [1 ]
Caporaso, A. [2 ,3 ]
Altieri, A. [1 ]
Indovina, P. [2 ,3 ,4 ,5 ]
Macaluso, M. [4 ,5 ]
Giordano, A. [2 ,3 ,4 ,5 ]
Pentimalli, F. [1 ]
机构
[1] IRCCS, Ist Nazl Tumori Fdn G Pascale, CROM, Naples, Italy
[2] Univ Siena, Dept Med Surg & Neurosci, Via Laterina 8, I-53100 Siena, Italy
[3] ITT, Siena, Italy
[4] Temple Univ, Sbarro Inst Canc Res & Mol Med, Coll Sci & Technol, BioLife Sci Bldg,Suite 333,1900N 12th St, Philadelphia, PA 19122 USA
[5] Temple Univ, Coll Sci & Technol, Ctr Biotechnol, BioLife Sci Bldg,Suite 333,1900N 12th St, Philadelphia, PA 19122 USA
关键词
DNA-DAMAGE RESPONSE; STRAND BREAK REPAIR; SPLICING-FACTOR; MESSENGER-RNA; CHK1; ACTIVATION; ATR ACTIVATION; RPA-SSDNA; PROTEIN; PHOSPHORYLATION; REPLICATION;
D O I
10.1038/onc.2015.107
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The main risk factor for skin cancer is ultraviolet (UV) exposure, which causes DNA damage. Cells respond to UV-induced DNA damage by activating the intra-S-phase checkpoint, which prevents replication fork collapse, late origin firing and stabilizes fragile sites. Recently, the 54-kDa multifunctional protein NONO was found to be involved in the non-homologous end-joining DNA repair process and in poly ADP-ribose polymerase 1 activation. Interestingly, NONO is mutated in several tumour types and emerged as a crucial factor underlying both melanoma development and progression. Therefore, we set out to evaluate whether NONO could be involved in the DNA-damage response to UV radiations. We generated NONO-silenced HeLa cell clones and found that lack of NONO decreased cell growth rate. Then, we challenged NONO-silenced cells with exposure to UV radiations and found that NONO-silenced cells, compared with control cells, continued to synthesize DNA, failed to block new origin firing and impaired CHK1S345 phosphorylation showing a defective checkpoint activation. Consistently, NONO is present at the sites of UV-induced DNA damage where it localizes to RAD9 foci. To position NONO in the DNA-damage response cascade, we analysed the loading onto chromatin of various intra-S-phase checkpoint mediators and found that NONO favours the loading of topoisomerase II-binding protein 1 acting upstream of the ATM and Rad3-related kinase activity. Strikingly, re-expression of NONO, through an sh-resistant mRNA, rescued CHK1S345 phosphorylation in NONO-silenced cells. Interestingly, NONO silencing affected cell response to UV radiations also in a melanoma cell line. Overall, our data uncover a new role for NONO in mediating the cellular response to UV-induced DNA damage.
引用
收藏
页码:567 / 576
页数:10
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