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CCAAT/增强子结合蛋白转录因子家族的DNA结合特异性

DNA binding specificity of the CCAAT/enhancer-binding protein transcription factor family.

作者信息

Osada S, Yamamoto H, Nishihara T, Imagawa M

机构信息

Department of Environmental Biochemistry, Faculty of Pharmaceutical Sciences, Osaka University, 1-6 Yamada-Oka, Suita, Osaka 565, Japan.

出版信息

J Biol Chem. 1996 Feb 16;271(7):3891-6. doi: 10.1074/jbc.271.7.3891.

Abstract

CCAAT/enhancer-binding protein (C/EBP) transcription factor family members are related by a high degree of amino acid sequence identity to the basic leucine zipper DNA-binding domain and show distinct but overlapping patterns of tissue- and stage-restricted expression. Although C/EBPalpha and C/EBPbeta have been shown to recognize a consensus sequence derived from regulatory elements in virus and acute-phase response genes, the potential for more subtle differences in the binding preference of the C/EBP family has not been previously addressed. The consensus sequence of C/EBPdelta has not been reported. By using the method of polymerase chain reaction-mediated random site selection to assess the DNA binding specificity of the C/EBP family in an unbiased manner, we demonstrated the sequence preferences for C/EBP family members. With small variations, these C/EBP family members showed similar sequence preferences, and the consensus sequence was identified as RTTGCGYAAY (R = A or G, and Y = C or T). The phosphorylation of C/EBPdelta by casein kinase II increased the binding activity, but did not affect the binding specificity, whereas it was reported that the phosphorylation of C/EBPalpha and C/EBPbeta decreased the binding affinity. The specificity of action of C/EBP family members may be derived from the characteristics of each factor, including the expression profiles, the DNA binding affinities, the cofactors, and so on, in addition to the DNA binding specificities.

摘要

CCAAT/增强子结合蛋白(C/EBP)转录因子家族成员在氨基酸序列上与碱性亮氨酸拉链DNA结合结构域高度同源,并呈现出不同但重叠的组织和阶段特异性表达模式。尽管C/EBPα和C/EBPβ已被证明能识别源自病毒和急性期反应基因调控元件的共有序列,但此前尚未探讨过C/EBP家族结合偏好中更细微差异的可能性。C/EBPδ的共有序列尚未见报道。通过使用聚合酶链反应介导的随机位点选择方法以无偏倚的方式评估C/EBP家族的DNA结合特异性,我们证明了C/EBP家族成员的序列偏好。虽有细微差异,但这些C/EBP家族成员表现出相似的序列偏好,且共有序列被确定为RTTGCGYAAY(R = A或G,Y = C或T)。酪蛋白激酶II对C/EBPδ的磷酸化增加了其结合活性,但不影响结合特异性,而据报道C/EBPα和C/EBPβ的磷酸化会降低结合亲和力。C/EBP家族成员的作用特异性可能除了DNA结合特异性之外,还源自每个因子的特性,包括表达谱、DNA结合亲和力、辅因子等等。

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