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果蝇copia反转录转座子包含同源异形蛋白进行转录调控的结合位点。

The Drosophila copia retrotransposon contains binding sites for transcriptional regulation by homeoproteins.

作者信息

Cavarec L, Heidmann T

机构信息

Unités de Physicochimie et Pharmacologie des Macromolécules Biologiques, CNRS U147 et INSERM U140, Institut Gustave Roussy, Villejuif, France.

出版信息

Nucleic Acids Res. 1993 Nov 11;21(22):5041-9. doi: 10.1093/nar/21.22.5041.

Abstract

We have identified in the 5' untranslated region of the Drosophila copia retrotransposon, 3' to the left LTR, a sequence for transcriptional regulation by homeoproteins. Co-transfection assays using expression vectors for homeoproteins and reporter vectors containing the lacZ gene under the control of either the entire copia LTR with 5' untranslated sequence, or a minimal heterologous promoter flanked with a 130 bp fragment containing the copia untranslated region, disclosed both positive and negative modulations of promoter activity in Drosophila cells in culture: a 5-10 fold decrease with engrailed, even-skipped and zerknüllt in DH33 cells, and a 10-30 fold increase with fushi tarazu and zerknüllt in Schneider II cells. In all cases, the regulatory effects were abolished with reporter plasmids deleted for a 58 bp fragment encompassing the putative homeoprotein binding sites. Mobility shift assays with a purified homeodomain-containing peptide demonstrated direct interaction with the 58 bp fragment, with an affinity in the 1-10 nM range as reported with the same peptide for other well characterized homeodomain binding regulatory sites. Foot-printing experiments with the extended LTR demonstrated protection of 'consensus' sequences, located within the 58 bp fragment. These homeodomain binding sites could be involved in the developmental regulation of the copia retrotransposon.

摘要

我们在果蝇copia逆转录转座子5'非翻译区中,位于左侧LTR的3'端,鉴定出一个受同源异形蛋白转录调控的序列。使用同源异形蛋白表达载体和报告载体进行共转染实验,报告载体包含在整个带有5'非翻译序列的copia LTR控制下的lacZ基因,或包含copia非翻译区的130 bp片段侧翼的最小异源启动子,结果显示在培养的果蝇细胞中启动子活性有正调控和负调控:在DH33细胞中,engrailed、even-skipped和zerknüllt会使活性降低5 - 10倍,而在Schneider II细胞中,fushi tarazu和zerknüllt会使活性增加10 - 30倍。在所有情况下,对于缺失包含假定同源异形蛋白结合位点的58 bp片段的报告质粒,调控作用均消失。用纯化的含同源结构域的肽进行迁移率变动分析表明,该肽与58 bp片段直接相互作用,亲和力在1 - 10 nM范围内,与该肽作用于其他特征明确的同源结构域结合调控位点时的情况相同。用延伸的LTR进行足迹实验表明,位于58 bp片段内的“共有”序列受到保护。这些同源结构域结合位点可能参与copia逆转录转座子的发育调控。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fcb/310615/aa1b3ed23d2b/nar00071-0068-a.jpg

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