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与海胆细胞质肌动蛋白基因CyIIa的相邻基因CyI和CyIIb相比,其与上游序列的蛋白质结合的修饰。

Modifications in protein binding to upstream sequences of the sea urchin cytoplasmic actin gene CyIIa in comparison to its linked neighbors, CyI and CyIIb.

作者信息

Katula K S, Dukes R L, Paul H, Franks R R

机构信息

Department of Biology, University of North Carolina at Greensboro, Greensboro, NC 27412, USA.

出版信息

Gene. 1998 Jun 15;213(1-2):195-203. doi: 10.1016/s0378-1119(98)00173-5.

Abstract

The sequences corresponding to regions upstream of the ATG and transcription start site of the CyIIa cytoplasmic actin gene of the sea urchin Strongylocentrotus purpuratus were determined and compared to the genomically linked CyI and CyIIb actin genes. Sites of protein-DNA interaction in the CyIIa upstream sequences were identified by DNase I footprinting. The similarity between CyIIa and CyI (and CyIIb) upstream sequences was limited and included a consensus octamer sequence, serum response element (SRE) and some short sequences within the proximal promoter region. The octamer sequence was found to bind protein. A single DNase I hypersensitive site was detected within the SRE and to two flanking nucleotides, but otherwise, the SRE did not appear to be protected. This is in contrast to strong protein binding to the CyIIb SRE. A region in the CyIIa gene with limited identity to the functionally significant protein binding site D in CyI also did not bind protein. Four additional sites of protein-DNA interaction were identified in CyIIa upstream sequences. One of these is similar to a protein binding site previously located in the CyI upstream sequences, whereas the others appear to be unique. These data indicate that the CyIIa upstream sequences differ extensively from those of CyI. The pattern of CyIIa expression is likely a consequence of these alternations in DNA sequence and protein-DNA interactions.

摘要

测定了紫海胆(Strongylocentrotus purpuratus)CyIIa细胞质肌动蛋白基因ATG上游区域和转录起始位点对应的序列,并将其与基因组连锁的CyI和CyIIb肌动蛋白基因进行比较。通过DNase I足迹法鉴定了CyIIa上游序列中蛋白质与DNA相互作用的位点。CyIIa与CyI(以及CyIIb)上游序列之间的相似性有限,包括一个共有八聚体序列、血清反应元件(SRE)以及近端启动子区域内的一些短序列。发现八聚体序列能结合蛋白质。在SRE内以及两个侧翼核苷酸处检测到一个单一的DNase I超敏位点,但除此之外,SRE似乎未受到保护。这与CyIIb SRE上强烈的蛋白质结合情况形成对比。CyIIa基因中与CyI中功能上重要的蛋白质结合位点D具有有限同源性的一个区域也未结合蛋白质。在CyIIa上游序列中还鉴定出另外四个蛋白质与DNA相互作用的位点。其中一个与先前在CyI上游序列中定位的一个蛋白质结合位点相似,而其他位点似乎是独特的。这些数据表明,CyIIa上游序列与CyI的上游序列有很大差异。CyIIa的表达模式可能是这些DNA序列和蛋白质与DNA相互作用变化的结果。

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