Ricci Claudia, Riolo Giulia, Marzocchi Carlotta, Brunetti Jlenia, Pini Alessandro, Cantara Silvia
Department of Medical, Surgical and Neurological Sciences, University of Siena, 53100 Siena, Italy.
Department of Medical Biotechnologies, University of Siena, 53100 Siena, Italy.
Biology (Basel). 2021 Sep 27;10(10):970. doi: 10.3390/biology10100970.
The tardigrade is an extremotolerant terrestrial invertebrate with a length of 0.1-1.0 mm. These small animals show an extraordinary tolerance to extreme conditions such as high pressure, irradiation, chemicals and dehydration. These abilities are linked to a recently discovered damage suppressor protein (Dsup). Dsup is a nucleosome-binding protein that avoids DNA damage after X-ray and oxidative stress exposure without impairing cell life in Dsup-transfected animal and plant cells. The exact "protective" role of this protein is still under study. In human cells, we confirmed that Dsup confers resistance to UV-C and HO exposure compared to untransfected cells. A different transcription factor activation was also observed. In addition, a different expression of endogenous genes involved in apoptosis, cell survival and DNA repair was found in Dsup+ cells after HO and UV-C. In UV-C exposed cells, Dsup efficiently upregulates DNA damage repair genes, while HO treatment only marginally involves the activation of pathways responsible for DNA repair in Dsup+ cells. These data are in agreement with the idea of a direct protective effect of the protein on DNA after oxidative stress. In conclusion, our data may help to outline the different mechanisms by which the Dsup protein works in response to different insults.
缓步动物是一种耐极端环境的陆生无脊椎动物,体长为0.1-1.0毫米。这些小动物对高压、辐射、化学物质和脱水等极端条件表现出非凡的耐受性。这些能力与最近发现的损伤抑制蛋白(Dsup)有关。Dsup是一种核小体结合蛋白,在X射线和氧化应激暴露后可避免DNA损伤,且不会损害Dsup转染的动植物细胞中的细胞活力。这种蛋白质的确切“保护”作用仍在研究中。在人类细胞中,我们证实与未转染的细胞相比,Dsup赋予了对UV-C和HO暴露的抗性。还观察到了不同的转录因子激活。此外,在HO和UV-C处理后的Dsup+细胞中,发现参与细胞凋亡、细胞存活和DNA修复的内源性基因表达不同。在UV-C暴露的细胞中,Dsup有效地上调DNA损伤修复基因,而HO处理仅略微涉及Dsup+细胞中负责DNA修复的途径的激活。这些数据与该蛋白质在氧化应激后对DNA具有直接保护作用的观点一致。总之,我们的数据可能有助于勾勒出Dsup蛋白响应不同损伤发挥作用的不同机制。