Jeffrey I W, Kadereit S, Meurs E F, Metzger T, Bachmann M, Schwemmle M, Hovanessian A G, Clemens M J
Division of Biochemistry, St. George's Hospital Medical School, London, United Kingdom.
Exp Cell Res. 1995 May;218(1):17-27. doi: 10.1006/excr.1995.1126.
The levels and subcellular distribution of the interferon-inducible double-stranded RNA-dependent protein kinase PKR have been measured in human Daudi cells and stably transfected mouse NIH 3T3 cells expressing the human protein kinase. Immunofluorescence of intact cells and quantitative immunoblotting of cell extracts indicate that PKR occurs in both the cytoplasm and the cell nucleus, with staining specifically in the nucleolus. The ratio of cytoplasmic to nuclear PKR is approximately 5:1 in control cells; in response to interferon treatment the protein kinase is induced severalfold in the cytoplasm whereas the level in the nucleus does not increase significantly. Analysis of individual transfected cells by confocal microscopy reveals a pattern of distribution of PKR similar to that in Daudi cells, with immunostaining of cytoplasm and nucleoli. Similar results are observed whether cells expressing wild-type PKR or a catalytically inactive mutant form of the kinase are analyzed, but untransfected 3T3 cells are not stained by the antibody used. Two-dimensional isoelectric focusing analysis of PKR in whole cell extracts reveals the presence of multiple forms with different pI values whereas similar analysis of the nuclear fraction indicates only one predominant species with a relatively basic pI. These results suggest that PKR may have a role in the cell nucleus as well as the cytoplasm and that the subcellular distribution of the protein kinase may be related to post-translational modifications.
已在人Daudi细胞和稳定转染表达人蛋白激酶的小鼠NIH 3T3细胞中检测了干扰素诱导的双链RNA依赖性蛋白激酶PKR的水平及其亚细胞分布。完整细胞的免疫荧光和细胞提取物的定量免疫印迹表明,PKR存在于细胞质和细胞核中,且在核仁中有特异性染色。在对照细胞中,细胞质与细胞核中PKR的比例约为5:1;在干扰素处理后,细胞质中的蛋白激酶诱导增加了几倍,而细胞核中的水平没有显著增加。通过共聚焦显微镜对单个转染细胞进行分析,发现PKR的分布模式与Daudi细胞中的相似,细胞质和核仁均有免疫染色。无论分析表达野生型PKR的细胞还是激酶的催化失活突变体形式的细胞,都观察到类似结果,但未转染的3T3细胞未被所用抗体染色。对全细胞提取物中的PKR进行二维等电聚焦分析,发现存在多种具有不同pI值的形式,而对细胞核部分的类似分析表明只有一种主要形式,其pI相对偏碱性。这些结果表明,PKR可能在细胞核以及细胞质中发挥作用,并且蛋白激酶的亚细胞分布可能与翻译后修饰有关。