Krause S, Fakan S, Weis K, Wahle E
Biozentrum der Universität Basal, Abteilung Zellbiologie, Switzerland.
Exp Cell Res. 1994 Sep;214(1):75-82. doi: 10.1006/excr.1994.1235.
During the polyadenylation of pre-mRNA in vitro, poly(A) binding protein II (PAB II) binds to the growing poly(A) tail, stimulating its extension. The subcellular localization of PAB II was investigated with an antibody affinity-purified from rabbit serum raised against the purified protein. Immunofluorescence microscopy detected PAB II exclusively in the cell nucleus, both in a widespread staining and in more intensely stained "speckles." PAB II was excluded from the nucleoli. By electron microscopy, PAB II was also found almost exclusively in the nucleus, predominantly in clusters of interchromatin granules, likely corresponding to the speckles observed by immunofluorescence microscopy, and in perichromatin fibrils, which represent nascent transcripts and probably the sites of pre-mRNA processing. In addition, electron microscopy also detected PAB II in nucleoli. The distribution corresponds largely to that of other factors involved in the processing of pre-mRNA and is thus in agreement with the proposed role of the protein in polyadenylation.
在体外前体mRNA的聚腺苷酸化过程中,聚(A)结合蛋白II(PAB II)与不断延长的聚(A)尾结合,刺激其延伸。用从针对纯化蛋白的兔血清中亲和纯化的抗体研究了PAB II的亚细胞定位。免疫荧光显微镜检查仅在细胞核中检测到PAB II,呈广泛染色以及染色更强烈的“斑点”状。PAB II被排除在核仁之外。通过电子显微镜观察,PAB II也几乎仅存在于细胞核中,主要存在于染色质间颗粒簇中,可能对应于免疫荧光显微镜观察到的斑点,以及存在于染色质周边纤维中,染色质周边纤维代表新生转录本,可能是前体mRNA加工的位点。此外,电子显微镜还在核仁中检测到了PAB II。其分布与参与前体mRNA加工的其他因子的分布基本一致,因此与该蛋白在聚腺苷酸化中的作用相符。