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SL3-3增强子因子1转录激活因子与病毒和染色体增强子序列的结合。

Binding of SL3-3 enhancer factor 1 transcriptional activators to viral and chromosomal enhancer sequences.

作者信息

Thornell A, Hallberg B, Grundström T

机构信息

Department of Applied Cell and Molecular Biology, University of Umeå, Sweden.

出版信息

J Virol. 1991 Jan;65(1):42-50. doi: 10.1128/JVI.65.1.42-50.1991.

Abstract

Interactions between SL3-3 enhancer factor 1 (SEF1) proteins and the enhancer of the murine leukemia virus SL3-3 were analyzed. SEF1 proteins were found to interact with two different DNA sequences within the DNA repeat region of the enhancer; these two motifs cooperated in enhancing initiation of transcription in T lymphocytes. Using an electrophoretic mobility shift assay, we identified nucleotides that are important for the SEF1 binding, and we deduced a sequence, 5'-TTTGCGGTTA/T-3' with highly improved binding of SEF1 proteins. We show that many different SEF1 binding sequences exist in the transcription control regions of different viral and cellular genes. The results indicate a general role of SEF1 proteins in T-cell gene expression.

摘要

分析了SL3-3增强子因子1(SEF1)蛋白与鼠白血病病毒SL3-3增强子之间的相互作用。发现SEF1蛋白与增强子DNA重复区域内的两个不同DNA序列相互作用;这两个基序协同增强T淋巴细胞中的转录起始。使用电泳迁移率变动分析,我们鉴定了对SEF1结合重要的核苷酸,并推导了一个序列5'-TTTGCGGTTA/T-3',其与SEF1蛋白的结合得到了高度改善。我们表明,在不同病毒和细胞基因的转录控制区域中存在许多不同的SEF1结合序列。结果表明SEF1蛋白在T细胞基因表达中具有普遍作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6b71/240487/9f9fb36b1b64/jvirol00044-0065-a.jpg

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