Czerwińska Jolanta, Poznański Jarosław, Dębski Janusz, Bukowy Zuzanna, Bohr Vilhelm A, Tudek Barbara, Speina Elżbieta
Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Pawińskiego 5a, 02-106 Warsaw, Poland.
National Institute on Aging, National Institutes of Health, 251 Bayview Blvd, Baltimore, MD 21224, USA.
Nucleic Acids Res. 2014;42(17):11119-35. doi: 10.1093/nar/gku783. Epub 2014 Aug 28.
4-Hydroxy-2-nonenal (HNE) is a reactive α,β-unsaturated aldehyde generated during oxidative stress and subsequent peroxidation of polyunsaturated fatty acids. Here, Werner protein (WRN) was identified as a novel target for modification by HNE. Werner syndrome arises through mutations in the WRN gene that encodes the RecQ DNA helicase which is critical for maintaining genomic stability. This hereditary disease is associated with chromosomal instability, premature aging and cancer predisposition. WRN appears to participate in the cellular response to oxidative stress and cells devoid of WRN display elevated levels of oxidative DNA damage. We demonstrated that helicase/ATPase and exonuclease activities of HNE-modified WRN protein were inhibited both in vitro and in immunocomplexes purified from the cell extracts. Sites of HNE adduction in human WRN were identified at Lys577, Cys727, His1290, Cys1367, Lys1371 and Lys1389. We applied in silico modeling of the helicase and RQC domains of WRN protein with HNE adducted to Lys577 and Cys727 and provided a potential mechanism of the observed deregulation of the protein catalytic activities. In light of the obtained results, we postulate that HNE adduction to WRN is a post-translational modification, which may affect WRN conformational stability and function, contributing to features and diseases associated with premature senescence.
4-羟基-2-壬烯醛(HNE)是一种在氧化应激以及多不饱和脂肪酸随后的过氧化过程中产生的反应性α,β-不饱和醛。在此,沃纳蛋白(WRN)被鉴定为HNE修饰的新靶点。沃纳综合征是由编码RecQ DNA解旋酶的WRN基因突变引起的,该酶对维持基因组稳定性至关重要。这种遗传性疾病与染色体不稳定、早衰和癌症易感性有关。WRN似乎参与细胞对氧化应激的反应,缺乏WRN的细胞显示出氧化DNA损伤水平升高。我们证明,在体外以及从细胞提取物中纯化的免疫复合物中,HNE修饰的WRN蛋白的解旋酶/ATP酶和核酸外切酶活性均受到抑制。在人WRN中,HNE加合位点被确定为赖氨酸577、半胱氨酸727、组氨酸1290、半胱氨酸1367、赖氨酸1371和赖氨酸1389。我们对WRN蛋白的解旋酶和RQC结构域与加合到赖氨酸577和半胱氨酸727的HNE进行了计算机模拟,并提供了观察到的蛋白质催化活性失调的潜在机制。根据所得结果,我们推测HNE与WRN的加合是一种翻译后修饰,可能影响WRN的构象稳定性和功能,导致与早衰相关的特征和疾病。