• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

Human protein binding to DNA sequences surrounding the human T-cell lymphotropic virus type-I long terminal repeat polyadenylation site.

作者信息

Levinger L F, Lautenberger J A

出版信息

Eur J Biochem. 1987 Aug 3;166(3):519-26. doi: 10.1111/j.1432-1033.1987.tb13544.x.

DOI:10.1111/j.1432-1033.1987.tb13544.x
PMID:3038544
Abstract

The long terminal repeats (LTRs) of RNA tumor viruses, including human T-cell lymphotropic virus type I (HTLV-I), contain the control elements for expression of viral genes. Sequence-specific LTR-DNA-binding proteins could regulate viral functions. To search for such proteins we have used an in vitro non-denaturing polyacrylamide gel assay, with restriction fragments of the HTLV-I LTR and nuclear protein extracts from several HTLV-I-infected cell lines and an uninfected T-cell line, H9. Four DNA-binding activities were observed, including non-specific DNA-binding activity and at least two activities (forms I and II) which bind specifically to a HinfI restriction fragment from nucleotides +181 to +334 relative to the transcription start site. DNA-binding activities I and II were partially resolved by ion-exchange chromatography and mapped by protection experiments to two 10-20-bp blocks surrounding the polyadenylation site at +221. Of the cell lines tested, form II was abundantly found in C10/MJ, and forms I and IV were also found in C91/PL, C81-66-45, MT2 and H9 cells.

摘要

相似文献

1
Human protein binding to DNA sequences surrounding the human T-cell lymphotropic virus type-I long terminal repeat polyadenylation site.
Eur J Biochem. 1987 Aug 3;166(3):519-26. doi: 10.1111/j.1432-1033.1987.tb13544.x.
2
Binding of host-cell factors to DNA sequences in the long terminal repeat of human T-cell leukemia virus type I: implications for viral gene expression.
Proc Natl Acad Sci U S A. 1988 Mar;85(5):1457-61. doi: 10.1073/pnas.85.5.1457.
3
Human T-cell leukemia virus types I and II exhibit different DNase I protection patterns.人类I型和II型T细胞白血病病毒表现出不同的脱氧核糖核酸酶I保护模式。
J Virol. 1988 Apr;62(4):1339-46. doi: 10.1128/JVI.62.4.1339-1346.1988.
4
Characterization of long terminal repeat sequences of HTLV-III.人类嗜T淋巴细胞病毒III型长末端重复序列的特征分析
Science. 1985 Feb 1;227(4686):538-40. doi: 10.1126/science.2981438.
5
Nucleotide sequence analysis of the long terminal repeat of human T-cell leukemia virus type II.人T细胞白血病病毒II型长末端重复序列的核苷酸序列分析
Proc Natl Acad Sci U S A. 1984 Feb;81(4):1079-83. doi: 10.1073/pnas.81.4.1079.
6
Avian retrovirus pp32 DNA-binding protein. I. Recognition of specific sequences on retrovirus DNA terminal repeats.禽逆转录病毒pp32 DNA结合蛋白。I. 对逆转录病毒DNA末端重复序列上特定序列的识别。
J Virol. 1982 Oct;44(1):330-43. doi: 10.1128/JVI.44.1.330-343.1982.
7
Two elements in the bovine leukemia virus long terminal repeat that regulate gene expression.牛白血病病毒长末端重复序列中调控基因表达的两个元件。
Science. 1986 Mar 21;231(4744):1437-40. doi: 10.1126/science.3006241.
8
Repetitive structure in the long-terminal-repeat element of a type II human T-cell leukemia virus.II型人类T细胞白血病病毒长末端重复元件中的重复结构。
Proc Natl Acad Sci U S A. 1984 Aug;81(15):4617-21. doi: 10.1073/pnas.81.15.4617.
9
Binding of cellular protein(s) to U3 region of human T-cell leukemia virus type-I long terminal repeat.细胞蛋白与人类I型T细胞白血病病毒长末端重复序列U3区域的结合。
Virus Genes. 1989 Aug;2(4):307-11. doi: 10.1007/BF00684038.
10
Preferential transcription of HTLV-I LTR in cell-free extracts of human T cells producing HTLV-I viral proteins.在产生人嗜T淋巴细胞病毒I型(HTLV-I)病毒蛋白的人T细胞无细胞提取物中,HTLV-I长末端重复序列(LTR)的优先转录。
Nucleic Acids Res. 1986 Jun 25;14(12):4779-86. doi: 10.1093/nar/14.12.4779.

引用本文的文献

1
Transcriptional suppression of the human T-cell leukemia virus type I long terminal repeat occurs by an unconventional interaction of a CREB factor with the R region.人T细胞白血病病毒I型长末端重复序列的转录抑制是通过一种CREB因子与R区域的非常规相互作用发生的。
Mol Cell Biol. 1994 Aug;14(8):5371-83. doi: 10.1128/mcb.14.8.5371-5383.1994.
2
Compilation of transcription regulating proteins.转录调节蛋白的汇编
Nucleic Acids Res. 1988 Mar 25;16(5):1879-902. doi: 10.1093/nar/16.5.1879.