Kawakami K, Mizumoto K, Ishihama A, Shinozaki-Yamaguchi K, Miura K
J Biochem. 1985 Feb;97(2):655-61. doi: 10.1093/oxfordjournals.jbchem.a135101.
During the generation of primer for transcription initiation by endonucleolytic cleavage of capped RNA, the influenza virus-associated RNA-dependent RNA polymerase recognizes three signals of capped RNA, i.e., cap-1 structure at 5' termini, RNA sequences at the cleavage sites, and distance between these two signals (Plotch, S.J., Bouloy, M., & Krug, R.M. (1979) Proc. Natl. Acad. Sci. U.S. 76, 1618-1622; Kawakami, K., Mizumoto, K., & Ishihama, A. (1983) Nucl. Acids Res. 11, 3637-3649). The free cap-1 structure, i.e., m7GpppNm not associated with polynucleotides, stimulates the RNA synthesis as well, irrespective of the presence or absence of dinucleotide primers. Since the stimulation by m7GpppNm and ApG is additive and the free cap-1 structure is not incorporated into 5' termini of product RNA, we propose that the cap-1 structure stimulates the RNA polymerase by allosteric modulation rather than by priming the transcription initiation.
在通过对带帽RNA进行核酸内切酶切割来生成转录起始引物的过程中,流感病毒相关的RNA依赖性RNA聚合酶识别带帽RNA的三个信号,即5'末端的帽-1结构、切割位点的RNA序列以及这两个信号之间的距离(Plotch, S.J., Bouloy, M., & Krug, R.M. (1979) Proc. Natl. Acad. Sci. U.S. 76, 1618 - 1622; Kawakami, K., Mizumoto, K., & Ishihama, A. (1983) Nucl. Acids Res. 11, 3637 - 3649)。游离的帽-1结构,即不与多核苷酸相关的m7GpppNm,也能刺激RNA合成,无论是否存在二核苷酸引物。由于m7GpppNm和ApG的刺激作用是相加的,并且游离的帽-1结构不会掺入产物RNA的5'末端,我们提出帽-1结构是通过变构调节而非引发转录起始来刺激RNA聚合酶的。