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[与RNA聚合酶活性中心共价结合的寡核苷酸的延伸]

[Elongation of oligonucleotides covalently bound to the active center of RNA polymerase].

作者信息

Zaĭchikov E F, Tsarev I G

出版信息

Bioorg Khim. 1988 Jan;14(1):121-4.

PMID:3382429
Abstract

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.

摘要

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。

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