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腺病毒12S和13S EIa信使核糖核酸的个别产物在转录水平上刺激病毒EIIa和EIII的表达。

Individual products of the adenovirus 12S and 13S EIa mRNAs stimulate viral EIIa and EIII expression at the transcriptional level.

作者信息

Leff T, Elkaim R, Goding C R, Jalinot P, Sassone-Corsi P, Perricaudet M, Kédinger C, Chambon P

出版信息

Proc Natl Acad Sci U S A. 1984 Jul;81(14):4381-5. doi: 10.1073/pnas.81.14.4381.

DOI:10.1073/pnas.81.14.4381
PMID:6336330
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC345593/
Abstract

Recombinant plasmids containing mutant or wild-type adenovirus serotype 2 EIa genes that produce the 12S mRNA alone, the 13S mRNA alone, or both mRNAs were cotransfected into HeLa cells with plasmids containing the viral EIIa or EIII transcription units. The amount of RNA produced from the EIIa and EIII promoters was increased by the products of both the 13S and the 12S RNAs. By measuring the level of specific transcription in nuclei isolated from transfected cells we directly demonstrate that the increased amount of EIIa RNA is due to stimulation of the rate of transcription.

摘要

将含有仅产生12S mRNA、仅产生13S mRNA或同时产生这两种mRNA的突变型或野生型腺病毒2型EIa基因的重组质粒,与含有病毒EIIa或EIII转录单位的质粒共转染到HeLa细胞中。13S和12S RNA的产物均增加了从EIIa和EIII启动子产生的RNA量。通过测量从转染细胞中分离出的细胞核中的特异性转录水平,我们直接证明EIIa RNA量的增加是由于转录速率的刺激。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8bb/345593/7090422fff9a/pnas00615-0151-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8bb/345593/26459c2a1495/pnas00615-0149-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8bb/345593/2c3fdb2a6610/pnas00615-0150-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8bb/345593/bc7a0ddc9f5c/pnas00615-0151-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8bb/345593/abb9ea6e4d85/pnas00615-0151-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8bb/345593/7090422fff9a/pnas00615-0151-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8bb/345593/26459c2a1495/pnas00615-0149-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8bb/345593/2c3fdb2a6610/pnas00615-0150-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8bb/345593/bc7a0ddc9f5c/pnas00615-0151-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8bb/345593/abb9ea6e4d85/pnas00615-0151-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f8bb/345593/7090422fff9a/pnas00615-0151-c.jpg

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1
Individual products of the adenovirus 12S and 13S EIa mRNAs stimulate viral EIIa and EIII expression at the transcriptional level.腺病毒12S和13S EIa信使核糖核酸的个别产物在转录水平上刺激病毒EIIa和EIII的表达。
Proc Natl Acad Sci U S A. 1984 Jul;81(14):4381-5. doi: 10.1073/pnas.81.14.4381.
2
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本文引用的文献

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The E1b promoter of Ad12 in mouse L tk- cells is activated by adenovirus region E1a.腺病毒12型(Ad12)在小鼠L tk-细胞中的E1b启动子被腺病毒E1a区域激活。
EMBO J. 1983;2(1):73-6. doi: 10.1002/j.1460-2075.1983.tb01383.x.
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The ovalbumin gene family: hormonal control of X and Y gene transcription and mRNA accumulation.卵清蛋白基因家族:X基因和Y基因转录及mRNA积累的激素调控
Cell. 1981 Feb;23(2):561-71. doi: 10.1016/0092-8674(81)90152-5.
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Adenovirus early gene products may control viral mRNA accumulation and translation in vivo.腺病毒早期基因产物可能在体内控制病毒mRNA的积累和翻译。
mRNA输出与人类C亚组腺病毒感染细胞中的转录激活相关。
J Virol. 1996 Jun;70(6):4071-80. doi: 10.1128/JVI.70.6.4071-4080.1996.
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Transcriptional activation by the adenovirus larger E1a product is mediated by members of the cellular transcription factor ATF family which can directly associate with E1a.腺病毒较大的E1a产物的转录激活是由细胞转录因子ATF家族的成员介导的,这些成员可以直接与E1a结合。
Mol Cell Biol. 1993 Jan;13(1):561-70. doi: 10.1128/mcb.13.1.561-570.1993.
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Down-regulation of HLA antigens by the adenovirus type 2 E3/19K protein in a T-lymphoma cell line.2型腺病毒E3/19K蛋白对T淋巴瘤细胞系中HLA抗原的下调作用
J Virol. 1994 Mar;68(3):1442-8. doi: 10.1128/JVI.68.3.1442-1448.1994.
6
Conserved cysteine residues within the E3/19K protein of adenovirus type 2 are essential for binding to major histocompatibility complex antigens.2型腺病毒E3/19K蛋白内保守的半胱氨酸残基对于与主要组织相容性复合体抗原的结合至关重要。
J Virol. 1994 Sep;68(9):5423-32. doi: 10.1128/JVI.68.9.5423-5432.1994.
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Complementary functions of E1a conserved region 1 cooperate with conserved region 3 to activate adenovirus serotype 5 early promoters.E1a保守区域1的互补功能与保守区域3协同作用以激活5型腺病毒早期启动子。
J Virol. 1994 Aug;68(8):4910-20. doi: 10.1128/JVI.68.8.4910-4920.1994.
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Modulation of transcriptional activation of the proliferating cell nuclear antigen promoter by the adenovirus E1A 243-residue oncoprotein depends on proximal activators.腺病毒E1A 243个氨基酸残基的癌蛋白对增殖细胞核抗原启动子转录激活的调节取决于近端激活因子。
Mol Cell Biol. 1994 Jan;14(1):543-53. doi: 10.1128/mcb.14.1.543-553.1994.
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Synthesis in Escherichia coli of human adenovirus type 12 transforming proteins encoded by early region 1A 13S mRNA and 12S mRNA.人12型腺病毒早期区域1A 13S信使核糖核酸和12S信使核糖核酸编码的转化蛋白在大肠杆菌中的合成。
Proc Natl Acad Sci U S A. 1984 Oct;81(20):6300-4. doi: 10.1073/pnas.81.20.6300.
Cell. 1981 Feb;23(2):485-96. doi: 10.1016/0092-8674(81)90144-6.
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Specific in vitro initiation of transcription on conalbumin and ovalbumin genes and comparison with adenovirus-2 early and late genes.伴清蛋白和卵清蛋白基因转录的特异性体外起始及与腺病毒2型早期和晚期基因的比较。
Nature. 1980 Jun 5;285(5764):367-73. doi: 10.1038/285367a0.
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Mechanism of activation of early viral transcription by the adenovirus E1A gene product.腺病毒E1A基因产物激活早期病毒转录的机制。
Cell. 1981 Oct;26(2 Pt 2):213-20. doi: 10.1016/0092-8674(81)90304-4.
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Transformation-defective mutant of adenovirus type 5 containing a single altered E1a mRNA species.含有单一改变的E1a mRNA种类的5型腺病毒转化缺陷型突变体。
J Virol. 1981 Dec;40(3):657-64. doi: 10.1128/JVI.40.3.657-664.1981.
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Resolving the functions of overlapping viral genes by site-specific mutagenesis at a mRNA splice site.通过在mRNA剪接位点进行位点特异性诱变来解析重叠病毒基因的功能。
Nature. 1982 Feb 4;295(5848):380-4. doi: 10.1038/295380a0.
8
Specific in vitro initiation of transcription on the adenovirus type 2 early and late EII transcription units.在腺病毒2型早期和晚期EII转录单元上进行特定的体外转录起始。
Proc Natl Acad Sci U S A. 1981 Dec;78(12):7383-7. doi: 10.1073/pnas.78.12.7383.
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Expression of early adenovirus genes requires a viral encoded acidic polypeptide.早期腺病毒基因的表达需要一种病毒编码的酸性多肽。
Proc Natl Acad Sci U S A. 1981 Oct;78(10):6121-5. doi: 10.1073/pnas.78.10.6121.
10
Specific in vitro transcription of conalbumin gene is drastically decreased by single-point mutation in T-A-T-A box homology sequence.伴清蛋白基因的特异性体外转录因T-A-T-A盒同源序列中的单点突变而急剧减少。
Proc Natl Acad Sci U S A. 1980 Dec;77(12):7024-8. doi: 10.1073/pnas.77.12.7024.