Petrova Daria V, Zateeva Maria V, Zhang Lijun, Zhang Jiajia, Zhao Ying, Permyakova Natalya V, Zagorskaya Alla A, Zharkov Vasily D, Endutkin Anton V, Yu Bing, Ma Chunquan, Li Haiying, Zharkov Dmitry O, Grin Inga R
Siberian Branch of the Russian Academy of Sciences Institute of Chemical Biology and Fundamental Medicine, 8 Lavrentieva Ave., 630090 Novosibirsk, Russia.
Engineering Research Center of Agricultural Microbiology Technology, Ministry of Education & Heilongjiang Provincial Key Laboratory of Plant Genetic Engineering and Biological Fermentation Engineering for Cold Region & Key Laboratory of Molecular Biology, College of Heilongjiang Province & School of Life Sciences, Heilongjiang University, Harbin 150080, China.
Int J Mol Sci. 2025 Aug 24;26(17):8221. doi: 10.3390/ijms26178221.
Uracil-DNA glycosylases (UNGs) are DNA repair enzymes responsible for the removal of uracil, a canonical RNA nucleobase, from DNA, where it appears through cytosine deamination or incorporation from the cellular dUTP pool. While human and UNGs have been extensively investigated, much less is known about their plant counterparts, of which UNGs from are the only studied examples. Here, we show that in sugar beet ( L.), an important crop species, cold and salt stress induce the expression of the gene () and modulate the level of the uracil-excising activity in the roots. Purified recombinant BvUNG efficiently removes uracil from DNA both in vitro and in an reporter strain but does not excise 5-hydroxyuracil, 5,6-dihydrouracil, or 5-hydroxymethyluracil. The activity is abolished by Ugi, a protein UNG inhibitor from PBS1 bacteriophage, and by a mutation of a conserved active site His residue. Structural modeling shows the presence of a disordered N-tail prone to undergo phase separation, followed by a long α helix oriented differently from its counterpart in human UNG. Overall, BvUNG is a functional uracil-DNA glycosylase that might participate in the response to abiotic stress.
尿嘧啶-DNA糖基化酶(UNGs)是一种DNA修复酶,负责从DNA中去除尿嘧啶(一种典型的RNA碱基),尿嘧啶可通过胞嘧啶脱氨基作用或从细胞dUTP库中掺入而出现在DNA中。虽然人类的UNGs已得到广泛研究,但对其植物同源物的了解却少得多,其中来自[具体植物名称未给出]的UNGs是唯一已被研究的例子。在此,我们表明,在重要农作物甜菜(Beta vulgaris L.)中,冷胁迫和盐胁迫会诱导BvUNG基因(Bv002449)的表达,并调节根中尿嘧啶切除活性的水平。纯化的重组BvUNG在体外和在大肠杆菌报告菌株中均能有效地从DNA中去除尿嘧啶,但不能切除5-羟基尿嘧啶、5,6-二氢尿嘧啶或5-羟甲基尿嘧啶。该活性被来自PBS1噬菌体的蛋白质UNG抑制剂Ugi以及保守活性位点组氨酸残基的突变所消除。结构建模显示存在一个易于发生相分离的无序N端尾巴,随后是一个与人类UNG中对应α螺旋方向不同的长α螺旋。总体而言,BvUNG是一种功能性尿嘧啶-DNA糖基化酶,可能参与对非生物胁迫的响应。