Pratt M A, Kralova J, McBurney M W
Department of Medicine, University of Ottawa, Ontario, Canada.
Mol Cell Biol. 1990 Dec;10(12):6445-53. doi: 10.1128/mcb.10.12.6445-6453.1990.
Pluripotential embryonal carcinoma cells such as those of the P19 line differentiate when exposed to retinoic acid (RA). The RAC65 cell line is a mutant clone of P19 cells selected to be RA nonresponsive. RAC65 cells carry a rearrangement affecting one of the genes encoding a nuclear retinoic acid receptor (RAR alpha). The mutant gene encodes a protein, RAR alpha', that has lost its 70 C-terminal amino acids, thus truncating the RA-binding domain. The RAR alpha' was found to be a dominant repressor of transcription from an RA-responsive target gene; however, expression of RAR alpha' was insufficient to confer RA nonresponsiveness, suggesting that RAC65 cells carry an additional mutation(s) affecting RA-induced genes.
多能胚胎癌细胞,如P19细胞系的细胞,在暴露于视黄酸(RA)时会发生分化。RAC65细胞系是从P19细胞中筛选出的对视黄酸无反应的突变克隆。RAC65细胞发生了重排,影响了编码核视黄酸受体(RARα)的其中一个基因。突变基因编码一种蛋白质,即RARα',它缺失了其70个C末端氨基酸,从而使视黄酸结合域截短。发现RARα'是视黄酸反应性靶基因转录的显性阻遏物;然而,RARα'的表达不足以导致对视黄酸无反应,这表明RAC65细胞携带另外一个影响视黄酸诱导基因的突变。