Appukuttan Deepti, Seo Ho Seong, Jeong Sunwook, Im Sunghun, Joe Minho, Song Dusup, Choi Jungjoon, Lim Sangyong
Research Division for Biotechnology, Korea Atomic Energy Research Institute, Jeongeup, Republic of Korea.
Department of Agricultural Biotechnology, Center for Agricultural Biomaterials, and Research Institute for Agriculture and Life Sciences, Seoul National University, Seoul, Republic of Korea.
PLoS One. 2015 Feb 23;10(2):e0118275. doi: 10.1371/journal.pone.0118275. eCollection 2015.
In order to understand the mechanism governing radiation resistance in Deinococcus radiodurans, current efforts are aimed at identifying potential candidates from a large repertoire of unique Deinococcal genes and protein families. DR0053 belongs to the DinB/YfiT protein family, which is an over-represented protein family in D. radiodurans. We observed that dr0053 transcript levels were highly induced in response to gamma radiation (γ-radiation) and mitomycin C (MMC) exposure depending on PprI, RecA and the DrtR/S two-component signal transduction system. Protein profiles demonstrated that DR0053 is a highly induced protein in cultures exposed to 10 kGy γ-radiation. We were able to determine the transcriptional start site of dr0053, which was induced upon irradiation, and to assign the 133-bp promoter region of dr0053 as essential for radiation responsiveness through primer extension and promoter deletion analyses. A dr0053 mutant strain displayed sensitivity to γ-radiation and MMC exposure, but not hydrogen peroxide, suggesting that DR0053 helps cells recover from DNA damage. Bioinformatic analyses revealed that DR0053 is similar to the Bacillus subtilis protein YjoA, which is a substrate of bacterial protein-tyrosine kinases. Taken together, the DNA damage-inducible (din) gene dr0053 may be regulated at the transcriptional and post-translational levels.
为了了解耐辐射球菌抗辐射的机制,目前的研究工作旨在从大量独特的耐辐射球菌基因和蛋白质家族中筛选出潜在的候选基因。DR0053属于DinB/YfiT蛋白质家族,该家族在耐辐射球菌中是一个高度富集的蛋白质家族。我们观察到,根据PprI、RecA和DrtR/S双组分信号转导系统,dr0053的转录水平在受到γ射线辐射(γ-辐射)和丝裂霉素C(MMC)处理时会高度上调。蛋白质谱分析表明,DR0053是在暴露于10 kGy γ-辐射的培养物中高度诱导表达的蛋白质。我们能够确定dr0053的转录起始位点,其在辐射后被诱导,并通过引物延伸和启动子缺失分析确定dr0053的133 bp启动子区域对辐射响应至关重要。一个dr0053突变株对γ-辐射和MMC处理敏感,但对过氧化氢不敏感,这表明DR0053有助于细胞从DNA损伤中恢复。生物信息学分析表明,DR0053与枯草芽孢杆菌的蛋白质YjoA相似,后者是细菌蛋白酪氨酸激酶的底物。综上所述,DNA损伤诱导型(din)基因dr0053可能在转录和翻译后水平受到调控。