Minton K W
J Exp Pathol. 1985 Fall;2(3):135-48.
Nature has provided the cell with an exquisite recognition mechanism in the ability of oligoribonucleotide polypyrimidine sequences to specifically bind to native duplex DNA polypurine X polypyrimidine stretches in a sequence specific fashion. This binding does not require DNA strand separation, since the oligoribonucleotide inserts into the DNA major grove where sequence-specific determinants are recognized. Thus far, there is no evidence in either prokaryotes or eukaryotes that this specificity plays a role in regulation of nucleic acid functions. Current understanding of prokaryotic transcription regulatory mechanisms is fairly detailed and appears to exclude this possibility. Our understanding of regulation of eukaryotic transcription is less advanced; possible sites for transcriptional inhibition by triple helix formation in eukaryotes include polypyrimidine stretches involved in termination of tRNA transcripts and premature termination of SV40 late mRNA transcripts.
自然界赋予细胞一种精妙的识别机制,即寡核糖核苷酸多嘧啶序列能够以序列特异性的方式与天然双链DNA多嘌呤X多嘧啶区段特异性结合。这种结合不需要DNA链分离,因为寡核糖核苷酸插入到DNA大沟中,在那里识别序列特异性决定因素。到目前为止,在原核生物或真核生物中都没有证据表明这种特异性在核酸功能的调控中起作用。目前对原核生物转录调控机制的理解相当详细,似乎排除了这种可能性。我们对真核生物转录调控的理解还不够深入;真核生物中通过三链螺旋形成进行转录抑制的可能位点包括参与tRNA转录本终止和SV40晚期mRNA转录本过早终止的多嘧啶区段。