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v-myb DNA结合结构域的特性分析

Characterization of the v-myb DNA binding domain.

作者信息

Oehler T, Arnold H, Biedenkapp H, Klempnauer K H

机构信息

Zentrum für Molekulare Biologie, Universität Heidelberg, FRG.

出版信息

Nucleic Acids Res. 1990 Apr 11;18(7):1703-10. doi: 10.1093/nar/18.7.1703.

DOI:10.1093/nar/18.7.1703
PMID:2110653
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC330586/
Abstract

The transforming protein encoded by the v-myb oncogene is a sequence-specific DNA-binding protein that is thought to be involved in the regulation of gene expression. The N-terminal region of the v-myb protein is composed of two highly conserved tandem repeat sequences of unknown function. It has been speculated that the N-terminal v-myb repeats might be crucial for DNA-binding, since N-terminal deletions destroy the DNA-binding activity of the v-myb protein. Here, we have studied the v-myb DNA-binding domain in more detail. Our results show that the N-terminal region of the v-myb protein is sufficient for specific DNA-binding. Dissection of this region suggests that both repeats are required for DNA-binding, but that both repeats play different roles in v-myb protein DNA interaction. We also show that the myb repeats of a drosophila melanogaster homolog of c-myb function as sequence-specific DNA-binding domain. Our results support the view that specific sequence-recognition, mediated by the conserved myb repeats, is a general feature of myb-related proteins.

摘要

由v-myb癌基因编码的转化蛋白是一种序列特异性DNA结合蛋白,被认为参与基因表达的调控。v-myb蛋白的N端区域由两个功能未知的高度保守串联重复序列组成。据推测,N端v-myb重复序列可能对DNA结合至关重要,因为N端缺失会破坏v-myb蛋白的DNA结合活性。在此,我们更详细地研究了v-myb DNA结合结构域。我们的结果表明,v-myb蛋白的N端区域足以实现特异性DNA结合。对该区域的剖析表明,两个重复序列对于DNA结合都是必需的,但两个重复序列在v-myb蛋白与DNA的相互作用中发挥不同作用。我们还表明,果蝇c-myb同源物的myb重复序列作为序列特异性DNA结合结构域发挥作用。我们的结果支持这样一种观点,即由保守的myb重复序列介导的特异性序列识别是myb相关蛋白的一个普遍特征。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aab5/330586/4e6b6463ec41/nar00191-0038-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aab5/330586/055ccc84d4ab/nar00191-0033-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aab5/330586/9cff63cd2e30/nar00191-0034-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aab5/330586/095fc556aea3/nar00191-0035-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aab5/330586/d7fb094c68be/nar00191-0037-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aab5/330586/4e6b6463ec41/nar00191-0038-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aab5/330586/055ccc84d4ab/nar00191-0033-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aab5/330586/9cff63cd2e30/nar00191-0034-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aab5/330586/095fc556aea3/nar00191-0035-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aab5/330586/d7fb094c68be/nar00191-0037-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/aab5/330586/4e6b6463ec41/nar00191-0038-a.jpg

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2
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Mutations in the DNA-binding and transcriptional activation domains of v-Myb cooperate in transformation.v-Myb的DNA结合域和转录激活域中的突变在转化过程中协同作用。
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引用本文的文献

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Oncogenic point mutations in the Myb DNA-binding domain alter the DNA-binding properties of Myb at a physiological target gene.Myb DNA结合结构域中的致癌点突变改变了Myb在生理靶基因上的DNA结合特性。
Nucleic Acids Res. 2007;35(21):7237-47. doi: 10.1093/nar/gkm675. Epub 2007 Oct 24.
2
The promoter regions of the Myb-regulated Adora2B and Mcm4 genes co-localize with origins of DNA replication.Myb调控的Adora2B和Mcm4基因的启动子区域与DNA复制起点共定位。
BMC Mol Biol. 2007 Sep 6;8:75. doi: 10.1186/1471-2199-8-75.
3
v-Myb mediates cooperation of a cell-specific enhancer with the mim-1 promoter.

本文引用的文献

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