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[在大肠杆菌RNA聚合酶系统中寡核苷酸模板上的重复多聚腺苷酸合成]

[Reiterative poly(A) synthesis on oligonucleotide templates in an Escherichia coli RNA-polymerase system].

作者信息

Denisova L Ia, Zagrebel'nyĭ S N, Pustoshilova N M

出版信息

Mol Biol (Mosk). 1980 Nov-Dec;14(6):1372-7.

PMID:7003355
Abstract

The poly(A) synthesis in the E. coli RNA-polymerase system on the oligothymidilates, oligouridilates and oligonucleotides d(5'-OH-CCATCTTTT-3'-OH) and d(5'-HO-TCTTTT-3'-OH) as templates was studied. The reaction was shown to proceed more intensively on the oligothymidilates compared to oligouridilates. The insertion of phosphate residues into 3' end of oligouridilates deteriorates properties of their templates though the length of the synthesized poly(A) is not changed in this case. The synthesis of poly(A) on the nonanucleotide d(CCATCTTTT) proceeds intensively, but there is no AMP incorporation on the hexanucleotide of similar structure. The author's data combined with certain literature results suppose that the template activity of the oligonucleotides containing homopolymer sequences is determined in the RNA-polymerase system in reiterative regime by two factors: by the total amount of oligonucleotide links and by the homopolymer block size. The total amount of links seems to be important for the oligonucleotide enzyme bind stability and must comprise not less than 6 charges of the phosphate groups. The homopolymer block size must be no less than of 4 links.

摘要

研究了大肠杆菌RNA聚合酶系统以寡聚胸苷酸、寡聚尿苷酸以及寡核苷酸d(5'-OH-CCATCTTTT-3'-OH)和d(5'-HO-TCTTTT-3'-OH)为模板的多聚(A)合成。结果表明,与寡聚尿苷酸相比,该反应在寡聚胸苷酸上进行得更强烈。将磷酸残基插入寡聚尿苷酸的3'末端会降低其模板性能,不过在这种情况下合成的多聚(A)长度不变。在九核苷酸d(CCATCTTTT)上多聚(A)的合成进行得很强烈,但在结构相似的六核苷酸上没有AMP掺入。作者的数据与某些文献结果表明,在RNA聚合酶系统的重复模式下,含有同聚物序列的寡核苷酸的模板活性由两个因素决定:寡核苷酸连接的总量和同聚物块的大小。连接的总量对于寡核苷酸与酶结合的稳定性似乎很重要,并且必须包含不少于6个磷酸基团的电荷。同聚物块的大小必须不少于4个连接。

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