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Molecular properties of Zic4 and Zic5 proteins: functional diversity within Zic family
被引:23
作者:
Ishiguro, A
Inoue, T
Mikoshiba, K
Aruga, J
[1
]
机构:
[1] RIKEN, Brain Sci Inst, Lab Comparat Neurogenesis, Wako, Saitama 3510198, Japan
[2] RIKEN, Brain Sci Inst, Dev Neurobiol Lab, Wako, Saitama 3510198, Japan
关键词:
Zic;
transcription;
zinc-finger protein;
nuclear localization;
I-mfa;
ZOC domain;
D O I:
10.1016/j.bbrc.2004.09.052
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
摘要:
The Zic-family proteins control various developmental processes. Previous studies have shown that Zic1, Zic2, and Zic3 can act as transcriptional regulators, and that their functions are repressed by I-mfa, which has been identified as a repressor for basic helix-loop-helix-type transcriptional factors. Here, we investigated the molecular properties of the Zic4 and Zic5 proteins. Zic4/Zic5 showed DNA-binding activity to the Gli-binding sequence, similar to Zic1/Zic2/Zic3 proteins. However, Zic4/Zic5 did not exhibit any significant transcriptional activation ability nor they bind to I-mfa differently from Zic1/Zic2/Zic3. The nuclear localization of Zic4/Zic5 was not affected by the presence of the I-mfa protein, whereas the Zic1/Zic2/Zic3 proteins were translocated to the cytoplasmic compartment in the presence of I-mfa. The difference may be attributable to the dissimilarity of the N-terminal region between the Zic1/Zic2/Zic3 and Zic4/Zic5 proteins, since the binding of the Zic1/Zic2/Zic3 proteins to I-mfa occurs through their N-terminal regions. (C) 2004 Elsevier Inc. All rights reserved.
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页码:302 / 307
页数:6
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