Kulesz-Martin M F, Lisafeld B, Huang H, Kisiel N D, Lee L
Department of Experimental Therapeutics, Roswell Park Cancer Institute, Buffalo, New York 14263.
Mol Cell Biol. 1994 Mar;14(3):1698-708. doi: 10.1128/mcb.14.3.1698-1708.1994.
We previously demonstrated that a wild-type alternatively spliced p53 (p53as) RNA exists in mouse cultured cells and normal mouse tissues at approximately 25 to 33% of the level of the major p53 RNA form. The alternative RNA transcript is 96 nucleotides longer than the major transcript as a result of alternative splicing of intron 10 sequences. The protein expected to be generated from the p53as transcript is 9 amino acids shorter than the major p53 protein and has 17 different amino acids at the carboxyl terminus. We report here that p53as protein exists in nontransformed and malignant epidermal cells and is localized to the nucleus. In addition, p53as protein is preferentially expressed during the G2 phase of the cell cycle and in cells with greater than G2 DNA content compared with the major p53 protein, which is preferentially expressed in G1. The p53as immunoreactivity is elevated and shifted to the G1 phase of the cell cycle following actinomycin D treatment of nontransformed cells but not malignant cells. In view of the dimerization and tetramerization of p53 protein which may be necessary for its DNA binding and transcriptional activation activities, the presence of p53as protein in cells has important implications for understanding the physiological function(s) of the p53 gene.
我们先前证明,野生型可变剪接的p53(p53as)RNA存在于小鼠培养细胞和正常小鼠组织中,其水平约为主要p53 RNA形式的25%至33%。由于内含子10序列的可变剪接,该可变RNA转录本比主要转录本长96个核苷酸。预计从p53as转录本产生的蛋白质比主要p53蛋白质短9个氨基酸,并且在羧基末端有17个不同的氨基酸。我们在此报告,p53as蛋白存在于未转化和恶性表皮细胞中,并定位于细胞核。此外,与主要在G1期优先表达的p53蛋白相比,p53as蛋白在细胞周期的G2期以及DNA含量大于G2的细胞中优先表达。用放线菌素D处理未转化细胞而非恶性细胞后,p53as免疫反应性升高并转移至细胞周期的G1期。鉴于p53蛋白的二聚化和四聚化可能是其DNA结合和转录激活活性所必需的,细胞中p53as蛋白的存在对于理解p53基因的生理功能具有重要意义。