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VA RNA与狼疮抗原La之间的相互作用:体外核糖核蛋白颗粒的形成。

Interaction between VA RNA and the lupus antigen La: formation of a ribonucleoprotein particle in vitro.

作者信息

Francoeur A M, Mathews M B

出版信息

Proc Natl Acad Sci U S A. 1982 Nov;79(22):6772-6. doi: 10.1073/pnas.79.22.6772.

Abstract

The small adenovirus-encoded VA RNAs occur as ribonucleoprotein (RNP) particles in association with a cellular protein antigen, La, recognized by the anti-La class of lupus sera [Lerner, M. R., Boyle, J. A., Hardin, J. A. & Steitz, J. A. (1981) Science 211, 400-402]. We have tentatively identified the La antigen as a HeLa cell phosphoprotein of Mr approximately equal to 45,000, present in infected and uninfected cells. The antigen appears not to be required for the transcription of VA RNAs in vitro. RNP particles that contain newly synthesized VA RNAs assemble rapidly in transcription extracts making VA RNA and also can be reconstituted from purified VA RNA and a source of La antigen. Variant forms of VA RNAI with sequence deletions and substitutions bind to the La antigen, suggesting that the recognition site includes the RNA termini or the sequences corresponding to the internal control region (promoter), or both. Upon reconstitution with fragments of VA RNAI, oligonucleotides from both the 5' and 3' termini bind to the antigen, but those from the control region do not. The terminal oligonucleotides of wild-type VA RNA can form a basepaired stem, but structures of comparable stability cannot be formed by the chimeric variant molecules. Therefore, the recognition site is probably the terminal nucleotides themselves rather than the stem structure.

摘要

小型腺病毒编码的VA RNA以核糖核蛋白(RNP)颗粒的形式存在,与一种细胞蛋白抗原La相关联,该抗原可被抗La类狼疮血清识别[勒纳,M.R.,博伊尔,J.A.,哈丁,J.A.和施泰茨,J.A.(1981年)《科学》211,400 - 402]。我们初步将La抗原鉴定为一种分子量约为45,000的HeLa细胞磷蛋白,存在于感染和未感染的细胞中。该抗原似乎不是体外VA RNA转录所必需的。含有新合成VA RNA的RNP颗粒在产生VA RNA的转录提取物中迅速组装,也可以由纯化的VA RNA和La抗原来源重新组装。具有序列缺失和替换的VA RNAI变体形式与La抗原结合,这表明识别位点包括RNA末端或与内部控制区(启动子)对应的序列,或两者都包括。用VA RNAI片段重新组装时,来自5'和3'末端的寡核苷酸都与抗原结合,但来自控制区的寡核苷酸则不结合。野生型VA RNA的末端寡核苷酸可以形成碱基配对的茎,但嵌合变体分子无法形成具有可比稳定性的结构。因此,识别位点可能是末端核苷酸本身而不是茎结构。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b848/347215/f4791916a698/pnas00461-0043-a.jpg

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