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与前体mRNA双链区域互补的mRNA序列。使用RNA汞化和巯基琼脂糖凝胶色谱法的杂交实验

[mRNA sequences complementary to the double-stranded regions of pre-mRNA. Hybridization experiments using RNA mercuriation and chromatography on sulfhydryl-Sepharose].

作者信息

Kramerov D A, Ryskov A P

出版信息

Mol Biol (Mosk). 1979 May-Jun;13(3):601-12.

PMID:460206
Abstract

It was demonstrated that 4--6% of the sequences of mouse cell pure polysomal poly (A)mRNA are able to form stable duplexes during hybridization with the excess of double-stranded structures of nuclear pre-mRNA (double-stranded RNA). Hybridization of mRNA with the excess of mercuriated double-stranded RNA and chromatography of the hybrids on sulfhydril-sepharose was investigated. It was found that only 7--11% of the molecules of polysomal poly(A)+mRNA are able to form thermostable hybrids with sequences of double-stranded RNA. It may be supposed that in the population of mRNA there are relatively few molecules (about 5%) which contain sequences originated from long hairpin structures of pre-mRNA. Moreover, probably, there is a number of mRNA molecules (about 5% of the mRNA population) which are complementary in the entire length to "non-hairpin" double-stranded regions of pre-mRNA.

摘要

已证明,小鼠细胞纯多核糖体多聚(A)mRNA的4%-6%的序列在与过量的核前体mRNA双链结构(双链RNA)杂交过程中能够形成稳定的双链体。研究了mRNA与过量的汞化双链RNA的杂交以及杂交体在巯基琼脂糖上的层析。发现只有7%-11%的多核糖体多聚(A)+mRNA分子能够与双链RNA序列形成热稳定杂交体。可以推测,在mRNA群体中,含有源自前体mRNA长发夹结构序列的分子相对较少(约5%)。此外,可能还有一些mRNA分子(约占mRNA群体的5%)在全长上与前体mRNA的“非发夹”双链区域互补。

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