Disabled-1 interacts with a novel developmentally regulated protocadherin

被引:53
作者
Homayouni, R [1 ]
Rice, DS [1 ]
Curran, T [1 ]
机构
[1] St Jude Childrens Res Hosp, Dept Dev Neurobiol, Memphis, TN 38105 USA
关键词
reeler; migration; cell adhesion; phosphotyrosine binding domain; NPxY motif; in situ hybridization; Celera discovery systems;
D O I
10.1006/bbrc.2001.5998
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
Disabled-1 (Dab1) is an intracellular adapter protein that mediates the effect of Reelin on neuronal migration and cell positioning during mammalian brain. development. To identify components of the Reelin-Dab1 signaling pathway, we searched for proteins that interact with Dab1 using a yeast two-hybrid strategy. We found that the Dab1 phosphotyrosine binding (PTB) domain interacts with a novel protocadherin, orthologous to human protocadherin 18. Mouse Pcdh18 (mPcdh18), which consists of four exons similar to other protocadherin family members, maps to chromosome 3. The deduced amino acid sequence of mPcdh18 contains six extracellular cadherin motifs, a single transmembrane region, and a large intracellular domain. The site of Dab1 interaction was localized to the C-terminal 243 residues of mPcdh18. Expression analyses revealed that mPcdh18 is present in a variety of tissues in the embryo, but in adult mice it is primarily expressed in lung and kidney. In embryonic brain, mPcdhl8 expression is temporally and spatially regulated. Our results indicate that mPcdhl8 participates in signaling pathways involving PTB-containing proteins and suggest that it may play a role during brain development. (C) 2001 Elsevier Science.
引用
收藏
页码:539 / 547
页数:9
相关论文
共 49 条
[1]   The mouse Ames waltzer hearing-loss mutant is caused by mutation of Pcdh15, a novel protocadherin gene [J].
Alagramam, KN ;
Murcia, CL ;
Kwon, HY ;
Pawlowski, KS ;
Wright, CG ;
Woychik, RP .
NATURE GENETICS, 2001, 27 (01) :99-102
[2]  
[Anonymous], 1994, METHODS YEAST GENETI
[3]   NF-protocadherin, a novel member of the cadherin superfamily, is required for Xenopus ectodermal differentiation [J].
Bradley, RS ;
Espeseth, A ;
Kintner, C .
CURRENT BIOLOGY, 1998, 8 (06) :325-334
[4]   Reelin is a ligand for lipoprotein receptors [J].
D'Arcangelo, G ;
Homayouni, R ;
Keshvara, L ;
Rice, DS ;
Sheldon, M ;
Curran, T .
NEURON, 1999, 24 (02) :471-479
[5]   A PROTEIN RELATED TO EXTRACELLULAR-MATRIX PROTEINS DELETED IN THE MOUSE MUTANT REELER [J].
DARCANGELO, G ;
MIAO, GG ;
CHEN, SC ;
SOARES, HD ;
MORGAN, JI ;
CURRAN, T .
NATURE, 1995, 374 (6524) :719-723
[6]   Disabled-2 inactivation is an early step in ovarian tumorigenicity [J].
Fazili, Z ;
Sun, WP ;
Mittelstaedt, S ;
Cohen, C ;
Xu, XX .
ONCOGENE, 1999, 18 (20) :3104-3113
[7]   DOSAGE-SENSITIVE MODIFIERS OF DROSOPHILA-ABL TYROSINE KINASE FUNCTION - PROSPERO, A REGULATOR OF AXONAL OUTGROWTH, AND DISABLED, A NOVEL TYROSINE KINASE SUBSTRATE [J].
GERTLER, FB ;
HILL, KK ;
CLARK, MJ ;
HOFFMANN, FM .
GENES & DEVELOPMENT, 1993, 7 (03) :441-453
[8]   μ-protocadherin, a novel developmentally regulated protocadherin with mucin-like domains [J].
Goldberg, M ;
Peshkovsky, C ;
Shifteh, A ;
Al-Awqati, Q .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (32) :24622-24629
[9]   Direct binding of Reelin to VLDL receptor and ApoE receptor 2 induces tyrosine phosphorylation of disabled-1 and modulates tau phosphorylation [J].
Hiesberger, T ;
Trommsdorff, M ;
Howell, BW ;
Goffinet, A ;
Mumby, MC ;
Cooper, JA ;
Herz, J .
NEURON, 1999, 24 (02) :481-489
[10]  
Hirano S, 1999, J NEUROSCI, V19, P995