Coutts R H, Buck K W
Nucleic Acids Res. 1985 Nov 11;13(21):7881-97. doi: 10.1093/nar/13.21.7881.
Nuclei and hypotonically leached extracts of nuclei prepared from tomato golden mosaic virus (TGMV)-infected Nicotiana benthamiana leaves have been used in in vitro DNA and RNA polymerisation reactions. The synthesis of virus-specific DNA was resistant to aphidicolin, sensitive to N-ethylmaleimide and dideoxy TTP, and stimulated by KC1 and ATP. Variably virion (+) and complementary (-) strand DNA of both the A and B genomic components were synthesised. Virus-specific RNA was synthesised in reactions which were initiated prior to nuclei isolation and leaching. From inhibitor studies and salt requirements RNA synthesis appeared to be catalysed by a DNA-dependent RNA polymerase type II enzyme. Both components of the TGMV genome were transcribed in a bidirectional fashion with a prevalence in some experiments of transcripts derived from DNA component A.
从感染番茄金色花叶病毒(TGMV)的本氏烟草叶片中制备的细胞核以及经低渗处理后浸出的细胞核提取物,已被用于体外DNA和RNA聚合反应。病毒特异性DNA的合成对阿非迪霉素具有抗性,对N-乙基马来酰亚胺和双脱氧TTP敏感,并受KCl和ATP刺激。合成了A和B基因组组分的可变病毒粒子(+)链和互补(-)链DNA。在细胞核分离和浸出之前起始的反应中合成了病毒特异性RNA。从抑制剂研究和盐需求来看,RNA合成似乎由一种II型DNA依赖性RNA聚合酶催化。TGMV基因组的两个组分都以双向方式转录,在某些实验中,源自DNA组分A的转录本占优势。