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人波形蛋白启动子中负调控元件的鉴定:人I型T细胞白血病病毒Tax蛋白的调节作用

Identification of a negative element in the human vimentin promoter: modulation by the human T-cell leukemia virus type I Tax protein.

作者信息

Salvetti A, Lilienbaum A, Li Z, Paulin D, Gazzolo L

机构信息

UMR30 Centre National de la Recherche Scientifique/Université Claude Bernard Lyon I, Faculté de Médecine A. Carrel, France.

出版信息

Mol Cell Biol. 1993 Jan;13(1):89-97. doi: 10.1128/mcb.13.1.89-97.1993.

DOI:10.1128/mcb.13.1.89-97.1993
PMID:8417364
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC358888/
Abstract

The vimentin gene is a member of the intermediate filament multigene family and encodes a protein expressed, in vivo, in all mesenchymal derivatives and, in vitro, in cell types of various origin. We have previously demonstrated that the expression of this growth-regulated gene could be trans activated by the 40-kDa Tax protein of HTLV-I (human T-cell leukemia virus type I) and that responsiveness to this viral protein was mediated by the presence of an NF-kappa B binding site located between -241 and -210 bp upstream of the mRNA cap site (A. Lilienbaum, M. Duc Dodon, C. Alexandre, L. Gazzolo, and D. Paulin, J. Virol. 64:256-263, 1990). These previous assays, performed with deletion mutants of the vimentin promoter linked to the chloramphenicol acetyltransferase gene, also revealed the presence of an upstream negative region between -529 and -241 bp. Interestingly, the inhibitory activity exerted by this negative region was overcome after cotransfection of a Tax-expressing plasmid. In this study, we further characterize the vimentin negative element and define the effect of the Tax protein on the inhibitory activity of this element. We first demonstrate that a 187-bp domain (-424 to -237 bp) behaves as a negative region when placed upstream either of the NF-kappa B binding site of vimentin or of a heterologous enhancer such as that present in the desmin gene promoter. The negative effect can be further assigned to a 32-bp element which is indeed shown to repress the basal or induced activity of the NF-kappa B binding site.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

波形蛋白基因是中间丝多基因家族的成员,编码一种在体内所有间充质衍生物中表达、在体外各种来源的细胞类型中表达的蛋白质。我们先前已证明,该生长调节基因的表达可被I型人T细胞白血病病毒(HTLV-I)的40 kDa Tax蛋白反式激活,并且对该病毒蛋白的反应性是由位于mRNA帽位点上游-241至-210 bp之间的NF-κB结合位点介导的(A. Lilienbaum、M. Duc Dodon、C. Alexandre、L. Gazzolo和D. Paulin,《病毒学杂志》64:256-263,1990年)。这些先前用与氯霉素乙酰转移酶基因相连的波形蛋白启动子缺失突变体进行的试验还揭示,在-529至-241 bp之间存在一个上游负调控区域。有趣的是,在共转染表达Tax的质粒后,该负调控区域施加的抑制活性被克服。在本研究中,我们进一步对波形蛋白负调控元件进行了表征,并确定了Tax蛋白对该元件抑制活性的影响。我们首先证明,一个187 bp的结构域(-424至-237 bp),当置于波形蛋白的NF-κB结合位点上游或异源增强子(如结蛋白基因启动子中存在的增强子)上游时,表现为一个负调控区域。这种负面影响可进一步归因于一个32 bp的元件,该元件确实被证明可抑制NF-κB结合位点的基础活性或诱导活性。(摘要截短于250词)

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02c3/358888/3bce317b709b/molcellb00013-0120-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02c3/358888/8d30c8b10f18/molcellb00013-0119-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02c3/358888/3bce317b709b/molcellb00013-0120-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02c3/358888/8d30c8b10f18/molcellb00013-0119-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/02c3/358888/3bce317b709b/molcellb00013-0120-a.jpg

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本文引用的文献

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Isolation and characterization of retrovirus from cell lines of human adult T-cell leukemia and its implication in the disease.从成人T细胞白血病细胞系中分离和鉴定逆转录病毒及其在该疾病中的意义。
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TGFbeta1 regulation of vimentin gene expression during differentiation of the C2C12 skeletal myogenic cell line requires Smads, AP-1 and Sp1 family members.在C2C12骨骼肌成肌细胞系分化过程中,转化生长因子β1(TGFbeta1)对波形蛋白基因表达的调控需要Smads、活化蛋白-1(AP-1)和Sp1家族成员。
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ZBP-89 represses vimentin gene transcription by interacting with the transcriptional activator, Sp1.ZBP-89通过与转录激活因子Sp1相互作用来抑制波形蛋白基因的转录。
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Detection and isolation of type C retrovirus particles from fresh and cultured lymphocytes of a patient with cutaneous T-cell lymphoma.从一名皮肤T细胞淋巴瘤患者的新鲜淋巴细胞和培养淋巴细胞中检测并分离C型逆转录病毒颗粒。
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Control of myogenesis in the mouse myogenic C2 cell line by medium composition and by insulin: characterization of permissive and inducible C2 myoblasts.通过培养基成分和胰岛素对小鼠成肌C2细胞系中肌生成的控制:许可性和诱导性C2成肌细胞的特性
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CAT constructions with multiple unique restriction sites for the functional analysis of eukaryotic promoters and regulatory elements.用于真核启动子和调控元件功能分析的具有多个独特限制位点的CAT构建体。
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