The ribosomal 5.8S RNA as a target site for p53 protein in cell differentiation and oncogenesis

被引:5
作者
AbouElela, S [1 ]
Nazar, RN [1 ]
机构
[1] UNIV GUELPH,DEPT MOL BIOL & GENET,GUELPH,ON N1G 2W1,CANADA
基金
加拿大自然科学与工程研究理事会;
关键词
protein synthesis; 5.8S rRNA; p53; elongation;
D O I
10.1016/S0304-3835(97)00196-1
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Previous studies have shown that the ribosomal 5.8S rRNA of human cells is partially methylated in a tissue-specific fashion, a modification which occurs largely or entirely in the cytoplasm. More recent studies have shown that the 5.8S rRNA forms a covalent linkage with tumor suppressor p53 protein and have suggested that this RNA plays a functional role in protein elongation. We now show that the expression of p53 protein in Schizosaccharomyces pombe results in cells which: morphologically resemble transformed cells expressing mutant 5.8S rRNA; are equally compromised in their ability to sustain protein synthesis, in vitro; and contain polyribosome profiles which strongly resemble the elevated profiles which also are observed with mutated 5.8S rRNA. Taken together, these results provide new physiological evidence of the possibility that the 5.8S rRNA is an important target in the control of ribosome function during cell differentiation and oncogenesis. (C) 1997 Elsevier Science Ireland Ltd.
引用
收藏
页码:23 / 28
页数:6
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