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人干扰素诱导的42kDa 2-5A合成酶的全长序列及表达

Full-length sequence and expression of the 42 kDa 2-5A synthetase induced by human interferon.

作者信息

Wathelet M, Moutschen S, Cravador A, DeWit L, Defilippi P, Huez G, Content J

出版信息

FEBS Lett. 1986 Feb 3;196(1):113-20. doi: 10.1016/0014-5793(86)80224-1.

Abstract

Interferon-induced 2-5A synthetases are probably involved in some antiviral actions of interferon. In human cells two different mRNAs (1.6, 1.8 kb long) coding for this protein are transcribed from the same gene and are produced by differential splicing. The relationship between the two mRNAs of different size and the active enzyme is not clear, nor is the cellular localization of the latter known. We have cloned a cDNA corresponding to the 1.6 kb RNA. This cDNA was sequenced and its complete coding region was subcloned into pSP64. The resulting plasmid was used to direct the synthesis of micrograms of capped RNA transcript after linearization in the 3'-non-coding region. A 39 kDa protein was synthesized when this RNA was translated in rabbit reticulocyte lysate. When this capped RNA was introduced by microinjection into Xenopus oocytes, production of 2-5A synthetase was clearly observed in the cytoplasm and 10-30% of the enzyme accumulated with time in the nucleoplasm. Analysis of cytoplasmic homogenates of these oocytes on a glycerol gradient revealed that the enzyme is fully active in the monomeric form.

摘要

干扰素诱导的2-5A合成酶可能参与了干扰素的某些抗病毒作用。在人类细胞中,编码该蛋白的两种不同mRNA(长度分别为1.6 kb和1.8 kb)从同一基因转录而来,是通过差异剪接产生的。两种不同大小的mRNA与活性酶之间的关系尚不清楚,后者在细胞内的定位也未知。我们克隆了一个与1.6 kb RNA对应的cDNA。对该cDNA进行了测序,并将其完整编码区亚克隆到pSP64中。所得质粒在3'-非编码区线性化后,用于指导合成微克级的加帽RNA转录本。当这种RNA在兔网织红细胞裂解物中翻译时,合成了一种39 kDa的蛋白质。当通过显微注射将这种加帽RNA引入非洲爪蟾卵母细胞时,在细胞质中明显观察到2-5A合成酶的产生,并且随着时间的推移,10%-30%的酶积累在核质中。对这些卵母细胞的细胞质匀浆在甘油梯度上进行分析表明,该酶以单体形式具有完全活性。

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