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EBNA-1:一种灵长类淋巴细胞的病毒诱导核抗原及其在果蝇细胞中的表达

EBNA-1: a virally induced nuclear antigen of primate lymphocytes and its expression in Drosophila cells.

作者信息

MacGillivray A J, Allday M J, Saunders S E, Sinclair J H

机构信息

School of Biological Sciences, University of Sussex, Brighton, UK.

出版信息

Br J Cancer Suppl. 1988 Dec;9:93-7.

PMID:2474313
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2149112/
Abstract

EBNA-1 is a nuclear antigen of lymphocytes infected by Epstein-Barr virus and whose size polymorphism correlates only with the strain of infecting virus and the length of the glycine-alanine copolymer encoded by the third internal repeat of the viral genome. The major antigenic determinant(s) also appear to reside in this region. We have been able to obtain efficient expression of this nuclear antigen in cultured Drosophila cells transfected with a cosmid carrying the EBNA-1 coding region, indicating that insect mechanisms recognise control sequences and transcripts of the herpes virus. The association of a vimertin-like protein of mol. wt. 46,000 with Drosophila cell nuclei has been found to vary with culture conditions and heat shock. We now find that the level and nuclear association of this protein also increase after transfection with either EBNA-1 or yolk protein DNA.

摘要

EBNA-1是受爱泼斯坦-巴尔病毒感染的淋巴细胞的一种核抗原,其大小多态性仅与感染病毒的毒株以及病毒基因组第三个内部重复序列编码的甘氨酸-丙氨酸共聚物的长度相关。主要抗原决定簇似乎也位于该区域。我们已经能够在用携带EBNA-1编码区的黏粒转染的培养果蝇细胞中高效表达这种核抗原,这表明昆虫机制能够识别疱疹病毒的调控序列和转录本。已发现一种分子量为46,000的类波形蛋白与果蝇细胞核的结合会随培养条件和热休克而变化。我们现在发现,在用EBNA-1或卵黄蛋白DNA转染后,这种蛋白的水平及其与细胞核的结合也会增加。

相似文献

1
EBNA-1: a virally induced nuclear antigen of primate lymphocytes and its expression in Drosophila cells.EBNA-1:一种灵长类淋巴细胞的病毒诱导核抗原及其在果蝇细胞中的表达
Br J Cancer Suppl. 1988 Dec;9:93-7.
2
Epstein-Barr virus nuclear antigen (EBNA): size polymorphism of EBNA 1.爱泼斯坦-巴尔病毒核抗原(EBNA):EBNA 1的大小多态性
J Gen Virol. 1985 Jul;66 ( Pt 7):1595-600. doi: 10.1099/0022-1317-66-7-1595.
3
Efficient expression of an Epstein-Barr nuclear antigen in Drosophila cells transfected with Epstein-Barr virus DNA.在转染了爱泼斯坦-巴尔病毒DNA的果蝇细胞中爱泼斯坦-巴尔核抗原的高效表达。
EMBO J. 1985 Nov;4(11):2955-9. doi: 10.1002/j.1460-2075.1985.tb04029.x.
4
Genetic and biochemical evidence that EBNA 2 interaction with a 63-kDa cellular GTG-binding protein is essential for B lymphocyte growth transformation by EBV.EBNA 2与一种63 kDa细胞GTG结合蛋白相互作用对于EBV诱导B淋巴细胞生长转化至关重要的遗传学和生物化学证据。
Virology. 1994 Nov 1;204(2):634-41. doi: 10.1006/viro.1994.1578.
5
The glycine-alanine repeating region is the major epitope of the Epstein-Barr nuclear antigen-1 (EBNA-1).甘氨酸-丙氨酸重复区域是爱泼斯坦-巴尔核抗原1(EBNA-1)的主要表位。
J Immunol. 1987 Jan 15;138(2):593-9.
6
The conserved domain CR2 of Epstein-Barr virus nuclear antigen leader protein is responsible not only for nuclear matrix association but also for nuclear localization.爱泼斯坦-巴尔病毒核抗原前导蛋白的保守结构域CR2不仅负责与核基质结合,还负责核定位。
Virology. 2001 Jan 20;279(2):401-13. doi: 10.1006/viro.2000.0715.
7
Modulation of expression of insulin and IGF-I receptor by Epstein-Barr virus and its gene products LMP and EBNA-2 in lymphocyte cell lines.爱泼斯坦-巴尔病毒及其基因产物LMP和EBNA-2对淋巴细胞系中胰岛素和IGF-I受体表达的调节作用
J Cell Physiol. 1993 Mar;154(3):486-95. doi: 10.1002/jcp.1041540306.
8
Rheumatoid arthritis synovial membrane contains a 62,000-molecular-weight protein that shares an antigenic epitope with the Epstein-Barr virus-encoded associated nuclear antigen.类风湿性关节炎滑膜含有一种分子量为62,000的蛋白质,该蛋白质与爱泼斯坦-巴尔病毒编码的相关核抗原有一个共同的抗原表位。
J Clin Invest. 1986 May;77(5):1539-47. doi: 10.1172/JCI112469.
9
Protein-protein interactions between Epstein-Barr virus nuclear antigen-LP and cellular gene products: binding of 70-kilodalton heat shock proteins.爱泼斯坦-巴尔病毒核抗原-LP与细胞基因产物之间的蛋白质-蛋白质相互作用:70千道尔顿热休克蛋白的结合
Virology. 1996 Jun 1;220(1):91-9. doi: 10.1006/viro.1996.0289.
10
The Epstein-Barr virus nuclear antigen-6 protein co-localizes with EBNA-3 and survival of motor neurons protein.爱泼斯坦-巴尔病毒核抗原6蛋白与EBNA-3和运动神经元存活蛋白共定位。
Virology. 2004 Jan 5;318(1):280-94. doi: 10.1016/j.virol.2003.09.032.

本文引用的文献

1
Induction of the synthesis of a 70,000 dalton mammalian heat shock protein by the adenovirus E1A gene product.腺病毒E1A基因产物诱导合成一种70,000道尔顿的哺乳动物热休克蛋白。
Cell. 1982 Jul;29(3):913-9. doi: 10.1016/0092-8674(82)90453-6.
2
Two Drosophila melanogaster proteins related to intermediate filament proteins of vertebrate cells.两种与脊椎动物细胞中间丝蛋白相关的黑腹果蝇蛋白。
J Cell Biol. 1981 Oct;91(1):175-83. doi: 10.1083/jcb.91.1.175.
3
A cis-acting element from the Epstein-Barr viral genome that permits stable replication of recombinant plasmids in latently infected cells.
来自爱泼斯坦-巴尔病毒基因组的一个顺式作用元件,其可使重组质粒在潜伏感染细胞中稳定复制。
Proc Natl Acad Sci U S A. 1984 Jun;81(12):3806-10. doi: 10.1073/pnas.81.12.3806.
4
Immortalization of monkey epithelial cells by specific fragments of Epstein-Barr virus DNA.爱泼斯坦-巴尔病毒DNA特定片段使猴上皮细胞永生化
Nature. 1984;309(5963):78-82. doi: 10.1038/309078a0.
5
A sensitive enzyme-linked immunosorbent assay (ELISA) against the major EBV-associated antigens. I. Correlation between ELISA and immunofluorescence titers using purified antigens.一种针对主要EBV相关抗原的灵敏酶联免疫吸附测定(ELISA)。I. 使用纯化抗原时ELISA与免疫荧光滴度之间的相关性。
J Immunol Methods. 1984 Feb 24;67(1):145-56. doi: 10.1016/0022-1759(84)90093-0.
6
One of two Epstein-Barr virus nuclear antigens contains a glycine-alanine copolymer domain.两种爱泼斯坦-巴尔病毒核抗原之一含有一个甘氨酸-丙氨酸共聚结构域。
Proc Natl Acad Sci U S A. 1983 Sep;80(18):5665-9. doi: 10.1073/pnas.80.18.5665.
7
Partial purification of the Epstein-Barr virus nuclear antigen(s).爱泼斯坦-巴尔病毒核抗原的部分纯化
J Biol Chem. 1983 Mar 25;258(6):3974-82.
8
Simian virus 40 and polyoma virus induce synthesis of heat shock proteins in permissive cells.猿猴病毒40和多瘤病毒可诱导允许性细胞中热休克蛋白的合成。
Mol Cell Biol. 1983 Jan;3(1):1-8. doi: 10.1128/mcb.3.1.1-8.1983.
9
"Western blotting": electrophoretic transfer of proteins from sodium dodecyl sulfate--polyacrylamide gels to unmodified nitrocellulose and radiographic detection with antibody and radioiodinated protein A.“蛋白质免疫印迹法”:蛋白质从十二烷基硫酸钠 - 聚丙烯酰胺凝胶电泳转移至未修饰的硝酸纤维素膜上,并用抗体和放射性碘化蛋白A进行放射自显影检测。
Anal Biochem. 1981 Apr;112(2):195-203. doi: 10.1016/0003-2697(81)90281-5.
10
Antibodies against a synthetic peptide identify the Epstein-Barr virus-determined nuclear antigen.针对合成肽的抗体可识别爱泼斯坦-巴尔病毒确定的核抗原。
Proc Natl Acad Sci U S A. 1984 Aug;81(15):4652-6. doi: 10.1073/pnas.81.15.4652.