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多瘤病毒DNA中的二级结构。

Secondary structures in polyoma DNA.

作者信息

Wu M, Manor H, Davidson N

出版信息

J Virol. 1979 Oct;32(1):334-8. doi: 10.1128/JVI.32.1.334-338.1979.

DOI:10.1128/JVI.32.1.334-338.1979
PMID:232183
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC353558/
Abstract

Three reproducible secondary-structure features were observed on single strands of polyoma virus DNA mounted for electron microscopy by the T4 gene 32 protein technique: (i) a hairpin fold-back extending from 92.9 +/- 0.8 to 95.0 +/- 0.7 map units; (ii) a small loop extending from 63.2 +/- 3.1 to 68.5 +/- 2.8 map units; and (iii) a big loop extending from 51.9 +/- 2.3 to 68.9 +/- 2.1 map units. Both loops are bounded by inverted repeat stems of length 40 +/- 20 base pairs. The stem sequences around 68.5 and 68.9 of the large and small loops overlap, either partially or completely. Several lines of evidence indicate that the inverted repeat stems of the two secondary-structure loops lie in the regions of polyoma virus DNA flanking and probably very close to the sequences that are spliced out in the formation of the late 16S and 18S messages, whereas the hairpin fold-back appears to map at a splicing point of an early message. These structures may therefore be important for the processing of the primary transcripts to form the early and late messages.

摘要

通过T4基因32蛋白技术制备用于电子显微镜观察的多瘤病毒DNA单链上,观察到三个可重复的二级结构特征:(i)一个发夹回折结构,从92.9±0.8至95.0±0.7图距单位延伸;(ii)一个小环,从63.2±3.1至68.5±2.8图距单位延伸;以及(iii)一个大环,从51.9±2.3至68.9±2.1图距单位延伸。两个环均由长度为40±20个碱基对的反向重复茎环界定。大小环68.5和68.9周围的茎环序列部分或完全重叠。几条证据表明,两个二级结构环的反向重复茎环位于多瘤病毒DNA侧翼区域,可能非常接近在晚期16S和18S信使形成过程中被剪接掉的序列,而发夹回折结构似乎位于早期信使的一个剪接位点处。因此,这些结构可能对初级转录本加工形成早期和晚期信使很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2838/353558/bb7eded056d8/jvirol00190-0345-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2838/353558/bb7eded056d8/jvirol00190-0345-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2838/353558/bb7eded056d8/jvirol00190-0345-a.jpg

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引用本文的文献

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2
A conserved base pairing involving an alternative splice site of SV40 and polyoma late RNA.一种涉及SV40和多瘤病毒晚期RNA可变剪接位点的保守碱基配对。
Nucleic Acids Res. 1987 Oct 26;15(20):8566. doi: 10.1093/nar/15.20.8566.

本文引用的文献

1
Use of gene 32 protein staining of single-strand polynucleotides for gene mapping by electron microscopy: application to the phi80d3ilvsu+7 system.利用单链多核苷酸的基因32蛋白染色通过电子显微镜进行基因定位:应用于phi80d3ilvsu+7系统。
Proc Natl Acad Sci U S A. 1975 Nov;72(11):4506-10. doi: 10.1073/pnas.72.11.4506.
2
Structure of the inverted terminal repetition of adenovirus type 2 DNA.2型腺病毒DNA反向末端重复序列的结构
J Virol. 1977 Feb;21(2):766-77. doi: 10.1128/JVI.21.2.766-777.1977.
3
Complementary sequences 1700 nucleotides apart form a ribonuclease III cleavage site in Escherichia coli ribosomal precursor RNA.
相隔1700个核苷酸的互补序列在大肠杆菌核糖体前体RNA中形成一个核糖核酸酶III切割位点。
Proc Natl Acad Sci U S A. 1978 Aug;75(8):3593-7. doi: 10.1073/pnas.75.8.3593.
4
Electron microscopic mapping of RNA transcribed from the late region of polyoma virus DNA.多瘤病毒DNA晚期区域转录的RNA的电子显微镜定位
J Virol. 1979 Oct;32(1):293-303. doi: 10.1128/JVI.32.1.293-303.1979.
5
Mapping of inverted repeated DNA sequences within the genome of simian virus 40.猿猴病毒40基因组内反向重复DNA序列的定位
Proc Natl Acad Sci U S A. 1977 Apr;74(4):1631-4. doi: 10.1073/pnas.74.4.1631.
6
Mapping of sequences with 2-fold symmetry on the simian virus 40 genome: a photochemical crosslinking approach.猿猴病毒40基因组上具有二重对称性序列的图谱绘制:一种光化学交联方法。
Proc Natl Acad Sci U S A. 1977 Apr;74(4):1363-7. doi: 10.1073/pnas.74.4.1363.