Fornace A J, Alamo I, Hollander M C
Radiation Oncology Branch, National Cancer Institute, Bethesda, MD 20892.
Proc Natl Acad Sci U S A. 1988 Dec;85(23):8800-4. doi: 10.1073/pnas.85.23.8800.
Hybridization subtraction at low ratios of RNA to cDNA was used to enrich for the cDNA of transcripts increased in Chinese hamster cells after UV irradiation. Forty-nine different cDNA clones were isolated. Most coded for nonabundant transcripts rapidly induced 2- to 10-fold after UV irradiation. Only 2 of the 20 cDNA clones sequenced matched known sequences (metallothionein I and II). The predicted amino acid sequence of one cDNA had two localized areas of homology with the rat helix-destabilizing protein. These areas of homology were at the two DNA-binding sites of this nucleic acid single-strand-binding protein. The induced transcripts were separated into two general classes. Class I transcripts were induced by UV radiation and not by the alkylating agent methyl methanesulfonate. Class II transcripts were induced by UV radiation and by methyl methanesulfonate. Many class II transcripts were induced also by H2O2 and various alkylating agents but not by heat shock, phorbol 12-tetradecanoate 13-acetate, or DNA-damaging agents which do not produce high levels of base damage. Since many of the cDNA clones coded for transcripts which were induced rapidly and only by certain types of DNA-damaging agents, their induction is likely a specific response to such damage rather than a general response to cell injury.
采用低RNA与cDNA比例的杂交扣除法,富集紫外线照射后中国仓鼠细胞中表达量增加的转录本的cDNA。分离得到49个不同的cDNA克隆。大多数编码的是非丰富转录本,在紫外线照射后迅速诱导增加2至10倍。在测序的20个cDNA克隆中,只有2个与已知序列(金属硫蛋白I和II)匹配。一个cDNA的预测氨基酸序列与大鼠解螺旋蛋白有两个局部同源区域。这些同源区域位于这种核酸单链结合蛋白的两个DNA结合位点。诱导的转录本分为两大类。I类转录本由紫外线辐射诱导,而不由烷基化剂甲磺酸甲酯诱导。II类转录本由紫外线辐射和甲磺酸甲酯诱导。许多II类转录本也由过氧化氢和各种烷基化剂诱导,但不由热休克、佛波酯12-十四烷酸酯13-乙酸酯或不会产生高水平碱基损伤的DNA损伤剂诱导。由于许多cDNA克隆编码的转录本是快速诱导的,且只由某些类型的DNA损伤剂诱导,因此它们的诱导可能是对这种损伤的特异性反应,而不是对细胞损伤的一般反应。