Shohat O, Greenberg M, Reisman D, Oren M, Rotter V
Department of Cell Biology, Weizmann Institute of Science, Rehovot, Israel.
Oncogene. 1987;1(3):277-83.
p53 is an oncogene product which has been shown to be directly involved in malignant transformation. Furthermore, it has been proposed that this protein plays an essential role in the control of cell proliferation. In the present study, we investigated the involvement of p53 in growth regulation of cells by employing anti-sense RNA methodology to inhibit p53 expression. Transfection with p53-specific constructs spanning the entire mRNA molecule or the 5' region of the gene led to reduced p53 protein synthesis. Clones derived from such transfected cells exhibited a slower rate of DNA synthesis, as assayed by incorporation of [3H]thymidine. In most cases, transfection of plasmids encoding anti-sense RNA eventually brought about the complete cessation of cell proliferation. No such effects were observed in L12 cells, which do not synthesize p53 and therefore do not depend on p53 expression for their growth, thus excluding the possibility of a non-specific toxic effect exerted by the anti-sense p53 RNA. These findings support the notion that p53 is essential for continuous cell proliferation.
p53是一种癌基因产物,已被证明直接参与恶性转化。此外,有人提出这种蛋白质在细胞增殖控制中起重要作用。在本研究中,我们通过采用反义RNA方法抑制p53表达,研究了p53在细胞生长调节中的作用。用跨越整个mRNA分子或基因5'区域的p53特异性构建体进行转染,导致p53蛋白合成减少。从这种转染细胞衍生的克隆表现出较慢的DNA合成速率,通过掺入[3H]胸苷来测定。在大多数情况下,编码反义RNA的质粒转染最终导致细胞增殖完全停止。在不合成p53且因此其生长不依赖p53表达的L12细胞中未观察到此类效应,从而排除了反义p53 RNA产生非特异性毒性作用的可能性。这些发现支持了p53对细胞持续增殖至关重要的观点。