Fibroblast growth factor-1 stimulation of quiescent NIH 3T3 cells increases G/T mismatch-binding protein expression

被引:7
作者
Donohue, PJ
Feng, SLY
Alberts, GF
Guo, Y
Peifley, KA
Hsu, DKW
Winkles, JA
机构
[1] AMER RED CROSS,HOLLAND LAB,DEPT MOL BIOL,ROCKVILLE,MD 20855
[2] GEORGE WASHINGTON UNIV,MED CTR,DEPT MOL BIOL & BIOCHEM,WASHINGTON,DC 20037
关键词
D O I
10.1042/bj3190009
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Polypeptide growth factors promote cell-cycle progression in part by the transcriptional activation of a diverse group of specific genes, We have used an mRNA differential-display approach to identify several fibroblast growth factor (FGF)-1 (acidic FGF)-inducible genes in NIH 3T3 cells, Here we report that one of these genes, called FGF-regulated (FR)-3, is predicted to encode G/T mismatch-binding protein (GTBP), a component of the mammalian DNA mismatch correction system. The murine GTBP gene is transiently expressed after FGF-1 or calf serum treatment, with maximal mRNA levels detected at 12 and 18 h post-stimulation. FGF-l-stimulated NIH 3T3 cells also express an increased amount of GTBP as determined by immunoblot analysis. These results indicate that elevated levels of GTBP may be required during the DNA synthesis phase of the cell cycle for efficient G/T mismatch recognition and repair.
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页码:9 / 12
页数:4
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