The GCM domain is a Zn-coordinating DNA-binding domain

被引:27
作者
Cohen, SX
Moulin, M
Schilling, O
Meyer-Klaucke, W
Schreiber, J
Wegner, M
Müller, CW
机构
[1] European Mol Biol Lab, Grenoble Outstn, F-38042 Grenoble 9, France
[2] European Mol Biol Lab, Hamburg Outstn, D-22603 Hamburg, Germany
[3] Univ Erlangen Nurnberg, Inst Biochem, D-91054 Erlangen, Germany
关键词
transcription factor; DNA-binding domain; Zn coordination; EXAFS;
D O I
10.1016/S0014-5793(02)03257-X
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
Glial cells missing (GCM) proteins form a small family of transcriptional regulators involved in different developmental processes. They contain a DNA-binding domain that is highly conserved from flies to mice and humans and consists of approximately 150 residues. The GCM domain of the mouse GCM homolog a was expressed in bacteria. Extended X-ray absorption fine structure and particle-induced X-ray emission analysis techniques showed the presence of two Zn atoms with four-fold coordination and cysteine/thistidine residues as ligands. Zn atoms can be removed from the GCM domain by the Zn chelator phenanthroline only under denaturating conditions. This suggests that the Zn ions are buried in the interior of the GCM domain and that their removal abolishes DNA-binding because it impairs the structure of the GCM domain. Our results define the GCM domain as a new type of Zn-coordinating, sequence-specific DNA-binding domain. (C) 2002 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:95 / 100
页数:6
相关论文
共 21 条
[1]   The gcm-motif: A novel DNA-binding motif conserved in Drosophila and mammals [J].
Akiyama, Y ;
Hosoya, T ;
Poole, AM ;
Hotta, Y .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (25) :14912-14916
[2]   Analysis of zinc binding sites in protein crystal structures [J].
Alberts, IL ;
Nadassy, K ;
Wodak, SJ .
PROTEIN SCIENCE, 1998, 7 (08) :1700-1716
[3]   The glial cells missing-1 protein is essential for branching morphogenesis in the chorioallantoic placenta [J].
Anson-Cartwright, L ;
Dawson, K ;
Holmyard, D ;
Fisher, SJ ;
Lazzarini, RA ;
Cross, JC .
NATURE GENETICS, 2000, 25 (03) :311-314
[4]   Zinc coordination sphere in biochemical zinc sites [J].
Auld, DS .
BIOMETALS, 2001, 14 (3-4) :271-313
[5]   The galvanization of biology: A growing appreciation for the roles of zinc [J].
Berg, JM ;
Shi, YG .
SCIENCE, 1996, 271 (5252) :1081-1085
[6]   CONSTRAINED AND RESTRAINED REFINEMENT IN EXAFS DATA-ANALYSIS WITH CURVED WAVE THEORY [J].
BINSTED, N ;
STRANGE, RW ;
HASNAIN, SS .
BIOCHEMISTRY, 1992, 31 (48) :12117-12125
[7]   Leaving no element of doubt: analysis of proteins using microPIXE [J].
Garman, E .
STRUCTURE WITH FOLDING & DESIGN, 1999, 7 (12) :R291-R299
[8]   Recognition of specific DNA sequences [J].
Garvie, CW ;
Wolberger, C .
MOLECULAR CELL, 2001, 8 (05) :937-946
[9]   Genetic ablation of parathyroid glands reveals another source of parathyroid hormone [J].
Günther, T ;
Chen, ZF ;
Kim, JS ;
Priemel, M ;
Rueger, JM ;
Amling, M ;
Moseley, JM ;
Martin, TJ ;
Anderson, DJ ;
Karsenty, G .
NATURE, 2000, 406 (6792) :199-203
[10]   GLIAL-CELLS MISSING - A BINARY SWITCH BETWEEN NEURONAL AND GLIAL DETERMINATION IN DROSOPHILA [J].
HOSOYA, T ;
TAKIZAWA, K ;
NITTA, K ;
HOTTA, Y .
CELL, 1995, 82 (06) :1025-1036