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正常和再生大鼠肝脏中核及多核糖体多聚腺苷酸化和非多聚腺苷酸化RNA的序列多样性

Sequence diversity of nuclear and polysomal polyadenylated and non-polyadenylated RNA in normal and regenerating rat liver.

作者信息

Grady L J, Campbell W P, North A B

出版信息

Eur J Biochem. 1981 Apr;115(2):241-5. doi: 10.1111/j.1432-1033.1981.tb05229.x.

Abstract

A DNA probe purified from RNA . DNA hybrids of total sham-operated liver RNA and non-repetitive DNA was used to show that nuclear poly(A)-rich RNA from sham-operated liver and from 2.5-h and 48-h regenerating liver contains about 50% of the complexity of total liver RNA. It was further shown that the differences between normal and regenerating liver, reported earlier from this laboratory, occur in the poly(A)-free fraction of nuclear RNA. At the polysome level it was found that polysomal RNA has one-third of the sequence diversity of total RNA and of this, approximately 65% can be accounted for by poly(A)-rich and 55% by poly(A)-free molecules. When DNA probes were prepared from hybrids formed using polysomal RNA from sham-operated liver and regenerating liver at 2.5 h and 48 h post-hepatectomy and then employed in reactions with homologous and heterologous RNAs, no differences were detectable between either normal and regenerating liver or regenerating liver at times during hypertrophy and hyperplasia.

摘要

从假手术肝脏总RNA与非重复DNA的RNA·DNA杂交体中纯化得到的DNA探针,用于显示假手术肝脏以及2.5小时和48小时再生肝脏的富含多聚腺苷酸(poly(A))的核RNA包含约50%的肝脏总RNA复杂性。进一步表明,本实验室先前报道的正常肝脏与再生肝脏之间的差异,出现在核RNA的无poly(A)部分。在多核糖体水平上发现,多核糖体RNA具有总RNA三分之一的序列多样性,其中约65%可由富含poly(A)的分子解释,55%可由无poly(A)的分子解释。当使用肝切除术后2.5小时和48小时假手术肝脏及再生肝脏的多核糖体RNA形成的杂交体制备DNA探针,然后用于与同源和异源RNA的反应时,在正常肝脏与再生肝脏之间或再生肝脏在肥大和增生期间的不同时间点之间均未检测到差异。

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