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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.

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/02c3/358888/8d30c8b10f18/molcellb00013-0119-a.jpg

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