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Stress response of a p53 homologue in the radioresistant Sf9 insect cells.

机译:耐辐射的Sf9昆虫细胞中p53同源物的应激反应。

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摘要

PURPOSE: To investigate homology and stress response of p53 (a 53 kDa tumor suppressor protein) orthologue in Sf9 Lepidopteran insect cell line that exhibits very high radioresistance. MATERIALS AND METHODS: Western immunoblotting, immunoprecipitation, degenerate RT-PCR (reverse transcription-polymerase chain reaction), electrophoretic gel mobility shift assay, flow cytometry and immuno-fluorescence microscopy were used for characterizing structural and functional features of Sfp53 (Spodoptera frugiperda p53) in gamma-irradiated or etoposide-treated Sf9 insect and BMG-1 (brain malignant glioma) human cells. Cells were pre-treated with caffeine for inhibiting ATM/ATR (ataxia-telangiectasia mutated protein/ATM and Rad-3-related protein) activation, wherever required. RESULTS: A 47-49 kDa protein band was observed with antibodies against three different epitopes, demonstrating conservation of respective domains in Sfp53. Immunoprecipitation also yielded similar-sized protein. Degenerate RT-PCR resulted in product of same size in both cell lines. Similar gel mobility shift of p53-binding oligonucleotide with BMG-1 and Sf9 cell lysates indicated analogous transcriptional activity of Sfp53. Constitutive Sfp53 level was higher than hp53 (human p53) and showed primarily cytoplasmic localization. Radiation-induced accumulation was considerably less in Sf9 even as an analogous ATM/ATR-dependent nuclear translocation was observed following gamma-irradiation and etoposide. CONCLUSIONS: A smaller-sized Sfp53 orthologue shows highly conserved native structure with DNA-binding, N-terminus and C-terminus domains, and has analogous p53 transcriptional activity. While its nuclear translocation and ATM/ATR dependence were similar to hp53, the cytoplasmic localization and subdued accumulation following gamma-irradiation indicate functional differences from human cells.
机译:目的:研究在具有很高抗辐射性的Sf9鳞翅目昆虫细胞系中p53(一种53 kDa的肿瘤抑制蛋白)直系同源物的同源性和应激反应。材料与方法:使用Western免疫印迹,免疫沉淀,简并RT-PCR(逆转录-聚合酶链反应),电泳凝胶迁移率测定,流式细胞术和免疫荧光显微镜来表征Sfp53(Spodoptera frugiperda p53)的结构和功能特征。 γ射线或依托泊苷治疗的Sf9昆虫和BMG-1(脑恶性神经胶质瘤)人细胞中的表达。在需要时,用咖啡因预处理细胞以抑制ATM / ATR(共济失调毛细血管扩张突变蛋白/ ATM和Rad-3相关蛋白)的活化。结果:用针对三种不同表位的抗体观察到一条47-49 kDa的蛋白带,表明Sfp53中各个结构域的保守性。免疫沉淀也产生相似大小的蛋白质。简并的RT-PCR在两种细胞系中产生相同大小的产物。具有BMG-1和Sf9细胞裂解物的p53结合寡核苷酸的类似凝胶迁移率变化表明Sfp53具有类似的转录活性。组成型Sfp53水平高于hp53(人p53),主要表现在细胞质定位。即使在γ-射线和依托泊苷的照射下观察到类似的依赖于ATM / ATR的核易位,Sf9中的辐射诱导积累也要少得多。结论:较小尺寸的Sfp53直向同源物显示具有DNA结合,N端和C端结构域的高度保守的天然结构,并且具有类似的p53转录活性。尽管它的核易位和ATM / ATR依赖性与hp53相似,但γ射线照射后的细胞质定位和柔和的堆积表明其与人细胞的功能不同。

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