Wdr12, a mouse gene encoding a novel WD-repeat protein with a notchless-like amino-terminal domain

被引:22
作者
Nal, B
Mohr, E
Da Silva, MI
Tagett, R
Navarro, C
Carroll, P
Depetris, D
Verthuy, C
Jordan, BR
Ferrier, P [1 ]
机构
[1] Univ Aix Marseille 2, INSERM, CNRS, Ctr Immunol Marseille Luminy,CIML, F-13288 Marseille, France
[2] INSERM, U 382, Inst Biol Dev Marseille, IBDM, F-13288 Marseille, France
[3] INSERM, Fac Med, Lab Genet Med & Dev, U 491, F-13385 Marseille, France
基金
澳大利亚研究理事会;
关键词
cDNA cloning; functional genomics; gene expression; Notch; WD repeat;
D O I
10.1006/geno.2001.6682
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The WD-repeat protein family consists of a large group of structurally related yet functionally diverse proteins found predominantly in eukaryotic cells. These factors contain several (4-16) copies of a recognizable amino-acid sequence motif (the WD unit) thought to be organized into a "propeller-like" structure involved in protein-protein regulatory interactions. Here, we report the cloning of a mouse cDNA, referred to as Wdr12, which encodes a novel WD-repeat protein of 423 amino acids. The WDR12 protein was predicted to contain seven WD units and a nuclear localization signal located within a protruding peptide between the third and fourth WD domains. The amino-terminal region shows similarity to that of the Notchless WD repeat protein. Sequence comparisons revealed WDR12 orthologs in various eukaryotic species. Wdr12 seems to correspond to a single-copy gene in the mouse genome, located within the C1-C2 bands of chromosome 1. These data, together with the results of Wdr12 gene expression studies and evidence of in vitro binding of WDR12 to the cytoplasmic domain of Notch1, led us to postulate a function for the WDR12 protein in the modulation of Notch signaling activity.
引用
收藏
页码:77 / 86
页数:10
相关论文
共 42 条
[1]   Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[2]   Notch signaling: Cell fate control and signal integration in development [J].
Artavanis-Tsakonas, S ;
Rand, MD ;
Lake, RJ .
SCIENCE, 1999, 284 (5415) :770-776
[3]  
BONHOMME F, 1989, GENETIC VARIANTS STR, P649
[4]   Differential gene expression in CD3ε- and RAG1-deficient thymuses:: definition of a set of genes potentially involved in thymocyte maturation [J].
Carrier, A ;
Nguyen, C ;
Victorero, G ;
Granjeaud, S ;
Rocha, D ;
Bernard, K ;
Miazek, A ;
Ferrier, P ;
Malissen, M ;
Naquet, P ;
Malissen, B ;
Jordan, BR .
IMMUNOGENETICS, 1999, 50 (5-6) :255-270
[5]   Notch signaling in T cell development [J].
Deftos, ML ;
Bevan, MJ .
CURRENT OPINION IN IMMUNOLOGY, 2000, 12 (02) :166-172
[6]   Signal transduction pathways regulating the development of αβT cells [J].
Farrar, MA ;
Doerfler, P ;
Sauer, K .
BIOCHIMICA ET BIOPHYSICA ACTA-REVIEWS ON CANCER, 1998, 1377 (03) :F35-F78
[7]   CHROMOSOMAL TRANSLOCATION IN T-CELL LEUKEMIA LINE HUT-78 RESULTS IN A MYC FUSION TRANSCRIPT [J].
FINGER, LR ;
HUEBNER, K ;
CANNIZZARO, LA ;
MCLEOD, K ;
NOWELL, PC ;
CROCE, CM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (23) :9158-9162
[8]   Natural and engineered disorders of lymphocyte development [J].
Fischer, A ;
Malissen, B .
SCIENCE, 1998, 280 (5361) :237-243
[9]   Functional genomic analysis of C-elegans chromosome I by systematic RNA interference [J].
Fraser, AG ;
Kamath, RS ;
Zipperlen, P ;
Martinez-Campos, M ;
Sohrmann, M ;
Ahringer, J .
NATURE, 2000, 408 (6810) :325-330
[10]   Folding a WD repeat propeller -: Role of highly conserved aspartic acid residues in the G protein β subunit and Sec13 [J].
Garcia-Higuera, I ;
Gaitatzes, C ;
Smith, TF ;
Neer, EJ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (15) :9041-9049