Collett M S, Leis J P, Smith M S, Faras A J
J Virol. 1978 May;26(2):498-509. doi: 10.1128/JVI.26.2.498-509.1978.
The avian retrovirus RNA-directed DNA polymerase contains an activity that is capable of removing hydrogen bonds from duplex nucleic acid molecules. This "unwinding-like" activity appears to be specific in its action, affecting RNA.DNA and DNA.DNA duplex molecules but not RNA.RNA duplexes. Studies with defined RNA.DNA hybrid molecules (e.g., Rous sarcoma virus RNA and complementary DNAs representing specific regions of the Rous sarcoma virus genome) and DNA.DNA duplexes indicate that, although this activity can remove a portion of the hydrogen bonds from these double-stranded structures, complete separation of complementary strands is not accomplished. The unwinding-like activity exhibits sensitivities to temperature and monovalent and divalent cation concentrations. It can also remove a specific large oligonucleotide from the 5' end of the viral genome subsequent to RNase H hydrolysis of viral RNA complexed to DNA present at that terminus. This reverse transcriptase-associated unwinding-like activity is discussed with respect to recently proposed models of retrovirus proviral DNA synthesis.
禽逆转录病毒RNA指导的DNA聚合酶具有一种活性,能够从双链核酸分子中去除氢键。这种“解旋样”活性在其作用上似乎具有特异性,影响RNA·DNA和DNA·DNA双链分子,但不影响RNA·RNA双链体。对特定RNA·DNA杂交分子(例如,劳氏肉瘤病毒RNA和代表劳氏肉瘤病毒基因组特定区域的互补DNA)和DNA·DNA双链体的研究表明,尽管这种活性可以从这些双链结构中去除一部分氢键,但互补链并未完全分离。这种解旋样活性对温度以及单价和二价阳离子浓度敏感。在对与该末端存在的DNA复合的病毒RNA进行核糖核酸酶H水解后,它还可以从病毒基因组的5'末端去除特定的大寡核苷酸。关于最近提出的逆转录病毒前病毒DNA合成模型,讨论了这种与逆转录酶相关的解旋样活性。