• 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

转录因子Sp1识别来自猴基因组的启动子序列,这些序列是猿猴病毒40启动子。

Transcription factor Sp1 recognizes promoter sequences from the monkey genome that are simian virus 40 promoter.

作者信息

Dynan W S, Saffer J D, Lee W S, Tjian R

出版信息

Proc Natl Acad Sci U S A. 1985 Aug;82(15):4915-9. doi: 10.1073/pnas.82.15.4915.

DOI:10.1073/pnas.82.15.4915
PMID:2991898
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC390468/
Abstract

A 440-base-pair fragment of African green monkey genomic DNA shares homology with the transcriptional regulatory region of simian virus 40 (SV40) and has been reported to direct transcription in vivo. We find that two regions within this fragment bind the promoter-specific cellular transcription factor Sp1 and are protected in DNase protection ("footprinting") experiments. As in SV40, binding occurs in regions containing multiple copies of the sequence GGGCGG. These regions, when fused to the proximal, or "TATA box," element of the herpes simplex virus thymidine kinase promoter, are able to direct Sp1-dependent transcription in vitro. The finding that Sp1 is capable of productive interaction with sequences taken from a cellular promoter supports the idea that Sp1 may play a role in modulating transcription of cellular genes.

摘要

一段440个碱基对的非洲绿猴基因组DNA片段与猿猴病毒40(SV40)的转录调控区域具有同源性,并且据报道在体内可指导转录。我们发现该片段内的两个区域可结合启动子特异性细胞转录因子Sp1,并且在DNA酶保护(“足迹”)实验中受到保护。与SV40一样,结合发生在含有多个GGGCGG序列拷贝的区域。这些区域与单纯疱疹病毒胸苷激酶启动子的近端或“TATA盒”元件融合后,能够在体外指导Sp1依赖性转录。Sp1能够与来自细胞启动子的序列进行有效相互作用这一发现支持了Sp1可能在调节细胞基因转录中发挥作用的观点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58b3/390468/f6e8f26163bc/pnas00355-0063-g.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58b3/390468/50aa36cf0e0e/pnas00355-0061-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58b3/390468/a4d0bca9d933/pnas00355-0061-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58b3/390468/b63cce6076e0/pnas00355-0061-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58b3/390468/caaaffa051b8/pnas00355-0061-d.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58b3/390468/89841b9030c0/pnas00355-0062-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58b3/390468/dfad40a0be92/pnas00355-0062-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58b3/390468/84d5881419e0/pnas00355-0063-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58b3/390468/d6bc0bef3367/pnas00355-0063-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58b3/390468/5fff030db177/pnas00355-0063-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58b3/390468/219d20dd0787/pnas00355-0063-d.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58b3/390468/fd41b33d8cab/pnas00355-0063-e.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58b3/390468/adc9943c8243/pnas00355-0063-f.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58b3/390468/f6e8f26163bc/pnas00355-0063-g.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58b3/390468/50aa36cf0e0e/pnas00355-0061-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58b3/390468/a4d0bca9d933/pnas00355-0061-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58b3/390468/b63cce6076e0/pnas00355-0061-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58b3/390468/caaaffa051b8/pnas00355-0061-d.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58b3/390468/89841b9030c0/pnas00355-0062-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58b3/390468/dfad40a0be92/pnas00355-0062-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58b3/390468/84d5881419e0/pnas00355-0063-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58b3/390468/d6bc0bef3367/pnas00355-0063-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58b3/390468/5fff030db177/pnas00355-0063-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58b3/390468/219d20dd0787/pnas00355-0063-d.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58b3/390468/fd41b33d8cab/pnas00355-0063-e.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58b3/390468/adc9943c8243/pnas00355-0063-f.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/58b3/390468/f6e8f26163bc/pnas00355-0063-g.jpg

相似文献

1
Transcription factor Sp1 recognizes promoter sequences from the monkey genome that are simian virus 40 promoter.转录因子Sp1识别来自猴基因组的启动子序列,这些序列是猿猴病毒40启动子。
Proc Natl Acad Sci U S A. 1985 Aug;82(15):4915-9. doi: 10.1073/pnas.82.15.4915.
2
DNA sequences similar to those around the simian virus 40 origin of replication are present in the monkey genome.与猿猴病毒40复制起点周围的序列相似的DNA序列存在于猴子基因组中。
Proc Natl Acad Sci U S A. 1981 Jan;78(1):95-9. doi: 10.1073/pnas.78.1.95.
3
trans activation of the simian virus 40 late promoter by large T antigen requires binding sites for the cellular transcription factor TEF-1.猿猴病毒40晚期启动子的反式激活需要细胞转录因子TEF-1的结合位点。
J Virol. 1991 Dec;65(12):6535-43. doi: 10.1128/JVI.65.12.6535-6543.1991.
4
Binding of the Sp1 transcription factor by the human Harvey ras1 proto-oncogene promoter.人Harvey ras1原癌基因启动子与Sp1转录因子的结合。
Science. 1986 Jun 13;232(4756):1410-3. doi: 10.1126/science.3012774.
5
Bidirectional SV40 transcription mediated by tandem Sp1 binding interactions.由串联Sp1结合相互作用介导的双向SV40转录。
Science. 1985 Nov 1;230(4725):511-7. doi: 10.1126/science.2996137.
6
Transcription factor Sp1 recognizes a DNA sequence in the mouse dihydrofolate reductase promoter.转录因子Sp1识别小鼠二氢叶酸还原酶启动子中的一个DNA序列。
Nature. 1986;319(6050):246-8. doi: 10.1038/319246a0.
7
Specific stimulation of simian virus 40 late transcription in vitro by a cellular factor binding the simian virus 40 21-base-pair repeat promoter element.一种结合猿猴病毒40 21碱基对重复启动子元件的细胞因子对猿猴病毒40晚期转录的体外特异性刺激。
Proc Natl Acad Sci U S A. 1987 Sep;84(17):6025-9. doi: 10.1073/pnas.84.17.6025.
8
Multiple specific contacts between a mammalian transcription factor and its cognate promoters.哺乳动物转录因子与其同源启动子之间的多种特异性相互作用。
Nature. 1984;312(5993):409-13. doi: 10.1038/312409a0.
9
Two leaky-late HSV-1 promoters differ significantly in structural architecture.两个渗漏晚期单纯疱疹病毒1型启动子在结构架构上存在显著差异。
Virology. 2000 Jun 20;272(1):191-203. doi: 10.1006/viro.2000.0365.
10
Sp1 binds to promoter sequences and activates herpes simplex virus 'immediate-early' gene transcription in vitro.Sp1与启动子序列结合,并在体外激活单纯疱疹病毒“立即早期”基因转录。
Nature. 1985;317(6033):179-82. doi: 10.1038/317179a0.

引用本文的文献

1
Identification of poly(ADP-ribose) polymerase-1 as a cell cycle regulator through modulating Sp1 mediated transcription in human hepatoma cells.通过调节 Sp1 介导的转录鉴定人肝癌细胞中的多聚(ADP-核糖)聚合酶 1 作为细胞周期调节剂。
PLoS One. 2013 Dec 19;8(12):e82872. doi: 10.1371/journal.pone.0082872. eCollection 2013.
2
An unbiased in vivo screen reveals multiple transcription factors that control HPV E6-regulated hTERT in keratinocytes.一项无偏倚的体内筛选揭示了多个转录因子,它们控制着角化细胞中 HPV E6 调节的 hTERT。
Virology. 2013 Nov;446(1-2):17-24. doi: 10.1016/j.virol.2013.07.014. Epub 2013 Aug 8.
3
Regulation of poly(ADP-ribose) polymerase-1 (PARP-1) gene expression through the post-translational modification of Sp1: a nuclear target protein of PARP-1.

本文引用的文献

1
DNA-dependent transcription of adenovirus genes in a soluble whole-cell extract.腺病毒基因在可溶性全细胞提取物中的DNA依赖性转录。
Proc Natl Acad Sci U S A. 1980 Jul;77(7):3855-9. doi: 10.1073/pnas.77.7.3855.
2
Organization and expression of eucaryotic split genes coding for proteins.编码蛋白质的真核生物断裂基因的组织与表达。
Annu Rev Biochem. 1981;50:349-83. doi: 10.1146/annurev.bi.50.070181.002025.
3
Transcription from SV 40-like monkey DNA sequences.源自猴类SV40样DNA序列的转录。
通过Sp1的翻译后修饰对聚(ADP-核糖)聚合酶-1(PARP-1)基因表达的调控:PARP-1的一种核靶蛋白
BMC Mol Biol. 2007 Oct 25;8:96. doi: 10.1186/1471-2199-8-96.
4
A conserved alpha-helical motif mediates the interaction of Sp1-like transcriptional repressors with the corepressor mSin3A.一个保守的α-螺旋基序介导了Sp1样转录抑制因子与共抑制因子mSin3A之间的相互作用。
Mol Cell Biol. 2001 Aug;21(15):5041-9. doi: 10.1128/MCB.21.15.5041-5049.2001.
5
Reduced O glycosylation of Sp1 is associated with increased proteasome susceptibility.Sp1的O-糖基化减少与蛋白酶体敏感性增加有关。
Mol Cell Biol. 1997 May;17(5):2550-8. doi: 10.1128/MCB.17.5.2550.
6
Identification of two factors required for transcription of the ovalbumin gene.鉴定卵清蛋白基因转录所需的两个因子。
Mol Cell Biol. 1986 Dec;6(12):4259-67. doi: 10.1128/mcb.6.12.4259-4267.1986.
7
Comparative anatomy of the human APRT gene and enzyme: nucleotide sequence divergence and conservation of a nonrandom CpG dinucleotide arrangement.人类APRT基因与酶的比较解剖学:核苷酸序列差异以及非随机CpG二核苷酸排列的保守性
Proc Natl Acad Sci U S A. 1987 May;84(10):3349-53. doi: 10.1073/pnas.84.10.3349.
8
Cell proliferation and expression of the transferrin receptor gene: promoter sequence homologies and protein interactions.细胞增殖与转铁蛋白受体基因的表达:启动子序列同源性及蛋白质相互作用
J Cell Biol. 1986 Nov;103(5):1781-8. doi: 10.1083/jcb.103.5.1781.
9
Interferon response element of the human gene 6-16.人类基因6-16的干扰素反应元件
EMBO J. 1988 Jan;7(1):85-92. doi: 10.1002/j.1460-2075.1988.tb02786.x.
10
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.
Nucleic Acids Res. 1984 Jun 11;12(11):4769-88. doi: 10.1093/nar/12.11.4769.
4
Simian virus 40 major late promoter: an upstream DNA sequence required for efficient in vitro transcription.猴病毒40主要晚期启动子:体外高效转录所需的上游DNA序列。
Mol Cell Biol. 1984 Jan;4(1):133-41. doi: 10.1128/mcb.4.1.133-141.1984.
5
Sequences controlling in vitro transcription of SV40 promoters.控制SV40启动子体外转录的序列。
EMBO J. 1983;2(12):2293-303. doi: 10.1002/j.1460-2075.1983.tb01737.x.
6
Mapping of the late promoter of simian virus 40.猿猴病毒40晚期启动子的定位
Proc Natl Acad Sci U S A. 1984 Jan;81(1):23-7. doi: 10.1073/pnas.81.1.23.
7
Mutational dissection of the 21 bp repeat region of the SV40 early promoter reveals that it contains overlapping elements of the early-early and late-early promoters.对SV40早期启动子21bp重复区域的突变分析表明,它包含早期-早期启动子和晚期-早期启动子的重叠元件。
Nucleic Acids Res. 1984 Jan 25;12(2):915-32. doi: 10.1093/nar/12.2.915.
8
The promoter-specific transcription factor Sp1 binds to upstream sequences in the SV40 early promoter.启动子特异性转录因子Sp1与SV40早期启动子中的上游序列结合。
Cell. 1983 Nov;35(1):79-87. doi: 10.1016/0092-8674(83)90210-6.
9
The repeated GC-rich motifs upstream from the TATA box are important elements of the SV40 early promoter.TATA框上游富含GC的重复基序是SV40早期启动子的重要元件。
Nucleic Acids Res. 1983 Apr 25;11(8):2447-64. doi: 10.1093/nar/11.8.2447.
10
Deletion mapping of DNA regions required for SV40 early region promoter function in vivo.体内SV40早期区域启动子功能所需DNA区域的缺失图谱分析。
J Mol Appl Genet. 1982;1(5):457-81.