Zaĭchikov E F, Tsarev I G
Bioorg Khim. 1988 Jan;14(1):121-4.
Elongation (mediated by RNA polymerase and NTPs) of the primer oligonucleotide residues, covalently fixed near the active centre of RNA polymerase, has been studied. Hepta- and octanucleotide residues covalently attached to beta-subunit could not be elongated (evidently, because the translocation step is prevented), whereas the same residues attached to sigma-subunit were easily elongated. It was concluded that ease of the oligonucleotide residue elongation is due to the dissociation of sigma-subunit from the transcription complex. The mechanism of this dissociation is discussed.
对引物寡核苷酸残基的延伸(由RNA聚合酶和NTP介导)进行了研究,这些残基共价固定在RNA聚合酶活性中心附近。共价连接到β亚基上的七核苷酸和八核苷酸残基无法延伸(显然是因为转位步骤被阻止),而连接到σ亚基上的相同残基则很容易延伸。得出的结论是,寡核苷酸残基延伸的难易程度是由于σ亚基从转录复合物中解离所致。讨论了这种解离的机制。