Beacon interacts with cdc2/cdc28-like kinases

被引:23
作者
Kantham, L [1 ]
Kerr-Bayles, L
Godde, N
Quick, M
Webb, R
Sunderland, T
Bond, J
Walder, K
Augert, G
Collier, G
机构
[1] Deakin Univ, Sch Hlth Sci, Metab Res Unit, Waurn Ponds, Vic 3217, Australia
[2] CTGF, Merck Sante, F-59120 Loos, France
[3] Autogen Ltd, Waurn Ponds, Vic 3217, Australia
关键词
beacon; CLK; cdc2/cdc28-like kinase; obesity; protein/protein interactions; SPR; yeast two-hybrid; ubiquitin; sentrin;
D O I
10.1016/S0006-291X(03)00549-7
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
Previously we found elevated beacon gene expression in the hypothalamus of obese Psammomys obesus. Beacon administration into the lateral ventricle of P. obesus stimulated food intake and body weight gain. In the current study we used yeast two-hybrid technology to screen for proteins in the human brain that interact with beacon. CLK4, an isoform of cdc2/cdc28-like kinase family of proteins, was identified as a strong interacting partner for beacon. Using active recombinant proteins and a surface plasmon resonance based detection technique, we demonstrated that the three members of this subfamily of kinases (CLK1, 2, and 4) all interact with beacon. Based on the known sequence and functional properties of beacon and CLKs, we speculate that beacon could either modulate the function of key regulatory molecules such as PTP1B or control the expression patterns of specific genes involved in the central regulation of energy metabolism. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:125 / 129
页数:5
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