Tissue-specific Spred-2 promoter activity characterized by a gene trap approach

被引:13
作者
Bundschu, K
Gattenlöhner, S
Knobeloch, KP
Walter, U
Schuh, K
机构
[1] Inst Klin Biochim & Pathobiochim, D-97080 Wurzburg, Germany
[2] Univ Frauenklin, D-97080 Wurzburg, Germany
[3] Univ Wurzburg, Inst Pathol, D-97080 Wurzburg, Germany
[4] Forschungsinst Mol Pharmakol, D-12207 Berlin, Germany
关键词
Spred-2; gene trap; promoter activity; X-Gal staining;
D O I
10.1016/j.modgep.2005.08.003
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Spreds (Sprouty-related proteins with an Ena/Vasodilator-stimulated phosphoprotein homology-1 domain) are a new protein family inhibiting the mitogen-activated protein kinase (MAPK) signaling pathway. Different RNA and protein studies already revealed an almost ubiquitous Spred-2 expression pattern. But until now, only few data were available on the in situ Spred-2 promoter activity. Here, we show a detailed in situ analysis of a mouse strain with a trapped Spred-2 gene, bringing a beta-galactosidase and neomycin fusion gene (beta-geo) under the control of the endogenous Spred-2 promoter. This allowed us to monitor Spred-2 promoter activity in practically every organ and their corresponding sub-compartments. X-Gal staining of newborn and adult mice revealed a nearly congruent Spred-2 promoter activity pattern. Our detailed data provide information for further studies of the still enigmatic physiological functions of Spred-2 in various organs by identifying the tissues with strong Spred-2 promoter activity. (C) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:247 / 255
页数:9
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