DCAMKL1, a brain-specific transmembrane protein on 13q12.3 that is similar to doublecortin (DCX)

被引:54
作者
Sossey-Alaoui, K [1 ]
Srivastava, AK [1 ]
机构
[1] Greenwood Genet Ctr, JC Self Res Inst Human Genet, Greenwood, SC 29646 USA
关键词
D O I
10.1006/geno.1998.5718
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
Mutations in the human doublecortin (DCX), a brain-specific putative signaling protein, cause X-Iinked lissencephaly and subcortical band heterotopia. A predicted 740-amino-acid protein from human brain has two distinct regions, an N-terminal 345-amino-acid region 78% similar to the DCX protein and a C-terminal 427-amino-acid region that contains two transmembrane domains and is 98% homologous to a rat Ca2+/calmodulin-dependent protein kinase. We have designated this protein DCAMKL1. It maps to chromosome 13q12.3-q13, within a 540-kb YAC clone containing markers D13S805 and D13S1164. Northern analysis detected three major transcript isoforms of the DCAMKL1 gene expressed differentially and predominantly in human fetal and adult brain and during mouse embryogenesis (11-17 dpc). These results and its homology with the DCX and Ca2+/calmodulin dependent kinase proteins suggest a likely role for DCAMKL1 transmembrane protein in developing and adult brain, possibly in a pathway of cortical development. (C) 1999 Academic Press.
引用
收藏
页码:121 / 126
页数:6
相关论文
共 11 条
[1]   IRIS COLOBOMA, PTOSIS, HYPERTELORISM, AND MENTAL-RETARDATION - A NEW SYNDROME [J].
BARAITSER, M ;
WINTER, RM .
JOURNAL OF MEDICAL GENETICS, 1988, 25 (01) :41-43
[2]   A classification scheme for malformations of cortical development [J].
Barkovich, AJ ;
Kuzniecky, RI ;
Dobyns, WB ;
Jackson, GD ;
Becker, LE ;
Evrard, P .
NEUROPEDIATRICS, 1996, 27 (02) :59-63
[3]   High-resolution YAC-Cosmid-STS map of human chromosome 13 [J].
Cayanis, E ;
Russo, JJ ;
Kalachikov, S ;
Ye, XL ;
Park, SH ;
Sunjevaric, I ;
Bonaldo, MD ;
Lawton, L ;
Venkatraj, VS ;
Schon, E ;
Soares, MB ;
Rothstein, R ;
Warburton, D ;
Edelman, IS ;
Zhang, PS ;
Efstratiadis, A ;
Fischer, SG .
GENOMICS, 1998, 47 (01) :26-43
[4]  
des Portes V, 1998, CELL, V92, P51
[5]   X-linked malformations of neuronal migration [J].
Dobyns, WB ;
Andermann, E ;
Andermann, F ;
CzapanskyBeilman, D ;
Dubeau, F ;
Dulac, O ;
Guerrini, R ;
Hirsch, B ;
Ledbetter, DH ;
Lee, NS ;
Motte, J ;
Pinard, JM ;
Radtke, RA ;
Ross, ME ;
Tampieri, D ;
Walsh, CA ;
Truwit, CL .
NEUROLOGY, 1996, 47 (02) :331-339
[6]   doublecortin, a brain-specific gene mutated in human X-linked lissencephaly and double cortex syndrome, encodes a putative signaling protein [J].
Gleeson, JG ;
Allen, KM ;
Fox, JW ;
Lamperti, ED ;
Berkovic, S ;
Scheffer, I ;
Cooper, EC ;
Dobyns, WB ;
Minnerath, SR ;
Ross, ME ;
Walsh, CA .
CELL, 1998, 92 (01) :63-72
[7]   Point mutations and an intragenic deletion in LIS1, the lissencephaly causative gene in isolated lissencephaly sequence and Miller-Dieker syndrome [J].
LoNigro, C ;
Chong, SS ;
Smith, ACM ;
Dobyns, WB ;
Carrozzo, R ;
Ledbetter, DH .
HUMAN MOLECULAR GENETICS, 1997, 6 (02) :157-164
[8]  
Nagase T, 1997, DNA Res, V4, P141, DOI 10.1093/dnares/4.2.141
[9]   PREVIOUSLY APPARENTLY UNDESCRIBED SYNDROME - SHALLOW ORBITS, PTOSIS, COLOBOMA, TRIGONOCEPHALY, GYRAL MALFORMATIONS, AND MENTAL AND GROWTH-RETARDATION [J].
RAMER, JC ;
LIN, AE ;
DOBYNS, WB ;
WINTER, R ;
AYME, S ;
PALLOTTA, R ;
LADDA, RL .
AMERICAN JOURNAL OF MEDICAL GENETICS, 1995, 57 (03) :403-409
[10]   BCM Search Launcher - An integrated interface to molecular biology data base search and analysis services available on the World Wide Web [J].
Smith, RF ;
Wiese, BA ;
Wojzynski, MK ;
Davidson, DB ;
Worley, KC .
GENOME RESEARCH, 1996, 6 (05) :454-462