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本文引用的文献

1
An RNA polymerase II transcription factor binds to an upstream element in the adenovirus major late promoter.一种RNA聚合酶II转录因子与腺病毒主要晚期启动子中的上游元件结合。
Cell. 1985 Dec;43(2 Pt 1):439-48. doi: 10.1016/0092-8674(85)90174-6.
2
Rapid and efficient site-specific mutagenesis without phenotypic selection.无需表型筛选的快速高效位点特异性诱变。
Proc Natl Acad Sci U S A. 1985 Jan;82(2):488-92. doi: 10.1073/pnas.82.2.488.
3
Interactions of cellular proteins involved in the transcriptional regulation of the human immunodeficiency virus.参与人类免疫缺陷病毒转录调控的细胞蛋白之间的相互作用。
EMBO J. 1987 Dec 1;6(12):3761-70. doi: 10.1002/j.1460-2075.1987.tb02711.x.
4
Ubiquitous upstream repression sequences control activation of the inducible arginase gene in yeast.普遍存在的上游抑制序列控制酵母中诱导型精氨酸酶基因的激活。
Proc Natl Acad Sci U S A. 1987 Jun;84(12):3997-4001. doi: 10.1073/pnas.84.12.3997.
5
Identification of a putative regulator of early T cell activation genes.早期T细胞激活基因假定调节因子的鉴定
Science. 1988 Jul 8;241(4862):202-5. doi: 10.1126/science.3260404.
6
Complete nucleotide sequences of functional clones of the AIDS virus.艾滋病病毒功能克隆的完整核苷酸序列。
AIDS Res Hum Retroviruses. 1987 Spring;3(1):57-69. doi: 10.1089/aid.1987.3.57.
7
An inducible transcription factor activates expression of human immunodeficiency virus in T cells.一种可诱导转录因子激活T细胞中人免疫缺陷病毒的表达。
Nature. 1987;326(6114):711-3. doi: 10.1038/326711a0.
8
The location of cis-acting regulatory sequences in the human T cell lymphotropic virus type III (HTLV-III/LAV) long terminal repeat.人嗜T细胞病毒III型(HTLV-III/LAV)长末端重复序列中顺式作用调节序列的定位
Cell. 1985 Jul;41(3):813-23. doi: 10.1016/s0092-8674(85)80062-3.
9
The Fos complex and Fos-related antigens recognize sequence elements that contain AP-1 binding sites.
Science. 1988 Mar 4;239(4844):1150-3. doi: 10.1126/science.2964084.
10
Activation of the HIV-1 LTR by T cell mitogens and the trans-activator protein of HTLV-I.T细胞有丝分裂原和人嗜T淋巴细胞病毒I型反式激活蛋白对HIV-1长末端重复序列的激活作用。
Science. 1987 Dec 11;238(4833):1575-8. doi: 10.1126/science.2825351.

在人类免疫缺陷病毒1型负调控元件内鉴定顺式作用抑制序列。

Identification of cis-acting repressive sequences within the negative regulatory element of human immunodeficiency virus type 1.

作者信息

Lu Y C, Touzjian N, Stenzel M, Dorfman T, Sodroski J G, Haseltine W A

机构信息

Division of Human Retrovirology, Dana-Farber Cancer Institute, Boston, Massachusetts.

出版信息

J Virol. 1990 Oct;64(10):5226-9. doi: 10.1128/JVI.64.10.5226-5229.1990.

DOI:10.1128/JVI.64.10.5226-5229.1990
PMID:2398545
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC248024/
Abstract

The negative regulatory element of human immunodeficiency virus type 1 is a 260-nucleotide-long sequence that decreases the rate of RNA transcription initiation specified by the long terminal repeat. This region has the potential to bind several cellular transcription factors. Here it is shown that sequences which recognize the NFAT-1 and USF cellular transcription factors contribute to this negative regulatory effect. The sequences within the negative regulatory element which resemble the AP-1 site and the URS do not negatively regulate human immunodeficiency virus long terminal repeat transcription initiation.

摘要

人类免疫缺陷病毒1型的负调控元件是一段260个核苷酸长的序列,它降低了由长末端重复序列指定的RNA转录起始速率。该区域有可能结合几种细胞转录因子。本文表明,识别NFAT-1和USF细胞转录因子的序列对这种负调控效应有贡献。负调控元件中类似于AP-1位点和URS的序列不会对人类免疫缺陷病毒长末端重复序列的转录起始产生负调控作用。