Characterization of the human neurocan gene, CSPG3

被引:17
作者
Prange, CK [1 ]
Pennacchio, LA [1 ]
Lieuallen, K [1 ]
Fan, WF [1 ]
Lennon, GG [1 ]
机构
[1] Univ Calif Lawrence Livermore Natl Lab, Ctr Human Genome, Biol & Biotechnol Res Program, Livermore, CA 94550 USA
关键词
brain; chromosomal mapping; proteoglycan; sequencing;
D O I
10.1016/S0378-1119(98)00455-7
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Neurocan is a chondroitin sulfate proteoglycan thought to be involved in the modulation of cell adhesion and migration. Its sequence has been determined previously in rat and mouse (Rauch et al., 1992. Cloning and primary structure of neurocan, a developmentally regulated, aggregating, chondroitin sulfate proteoglycan of the brain. J. Biol. Chem. 267, 19536-19547; Rauch et al., 1995. Structure and chromosomal location of the mouse neurocan gene. Genomics 28, 405-410). We describe here the complete coding sequence of the human neurocan mRNA, known as CSPG3, as well as mapping data, expression analysis, and genomic structure. A cDNA known as CP-1 was initially sequenced as part of a gene discovery project focused on characterizing chromosome 19-specifrc cDNAs. Sequence homology searches indicated close homology to the mouse and rat proteoglycan, neurocan (GenBank accession Nos X84727 and M97161). Northern analysis identified a brain-specific transcript of approx. 7.5 kb. A longer cDNA clone, GT-5, was obtained, fine-mapped to the physical map of chromosome 19 by hybridization to a chromosome-specific cosmid library, and sequenced. Full coding sequence of the mRNA indicates a 3963 bp open reading frame corresponding to a 1321 amino acid protein, similar to the protein length found in mouse and rat. The amino acid sequence of human neurocan shows 63% identity with both the mouse and rat sequences. Finally, genomic sequencing of a cosmid containing the complete neurocan gene was performed to determine the genomic structure of the gene, which spans approx. 41 kb, and is transcribed in the telomere to centromere orientation. (C) 1998 Published by Elsevier Science B.V. Al rights reserved.
引用
收藏
页码:199 / 205
页数:7
相关论文
共 18 条
[1]   AN INTEGRATED METRIC PHYSICAL MAP OF HUMAN-CHROMOSOME-19 [J].
ASHWORTH, LK ;
BATZER, MA ;
BRANDRIFF, B ;
BRANSCOMB, E ;
DEJONG, P ;
GARCIA, E ;
GARNES, JA ;
GORDON, LA ;
LAMERDIN, JE ;
LENNON, G ;
MOHRENWEISER, H ;
OLSEN, AS ;
SLEZAK, T ;
CARRANO, AV .
NATURE GENETICS, 1995, 11 (04) :422-427
[2]   A HIGH-RESOLUTION, FLUORESCENCE-BASED, SEMIAUTOMATED METHOD FOR DNA FINGERPRINTING [J].
CARRANO, AV ;
LAMERDIN, J ;
ASHWORTH, LK ;
WATKINS, B ;
BRANSCOMB, E ;
SLEZAK, T ;
RAFF, M ;
DEJONG, PJ ;
KEITH, D ;
MCBRIDE, L ;
MEISTER, S ;
KRONICK, M .
GENOMICS, 1989, 4 (02) :129-136
[3]   RAPID ARRAYED FILTER PRODUCTION USING THE ORCA ROBOT [J].
COPELAND, A ;
LENNON, G .
NATURE, 1994, 369 (6479) :421-422
[4]  
DEJONG PJ, 1989, CYTOGENET CELL GENET, V51, P985
[5]   NEURONAL CHONDROITIN SULFATE PROTEOGLYCAN NEUROCAN BINDS TO THE NEURAL CELL-ADHESION MOLECULES NG-CAM/L1/NILE AND N-CAM, AND INHIBITS NEURONAL ADHESION AND NEURITE OUTGROWTH [J].
FRIEDLANDER, DR ;
MILEV, P ;
KARTHIKEYAN, L ;
MARGOLIS, RK ;
MARGOLIS, RU ;
GRUMET, M .
JOURNAL OF CELL BIOLOGY, 1994, 125 (03) :669-680
[6]   FUNCTIONAL-CHARACTERIZATION OF CHONDROITIN SULFATE PROTEOGLYCANS OF BRAIN - INTERACTIONS WITH NEURONS AND NEURAL CELL-ADHESION MOLECULES [J].
GRUMET, M ;
FLACCUS, A ;
MARGOLIS, RU .
JOURNAL OF CELL BIOLOGY, 1993, 120 (03) :815-824
[7]  
GRUMET M, 1994, J BIOL CHEM, V269, P12142
[8]  
MEYERPUTTLITZ B, 1995, J NEUROCHEM, V65, P2327
[9]   TAG-1/axonin-1 is a high-affinity ligand of neurocan, phosphacan/protein-tyrosine phosphatase-zeta/beta, and N-CAM [J].
Milev, P ;
Maurel, P ;
Haring, M ;
Margolis, RK ;
Margolis, RU .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (26) :15716-15723
[10]   PEANUT AGGLUTININ AND CHONDROITIN-6-SULFATE ARE MOLECULAR MARKERS FOR TISSUES THAT ACT AS BARRIERS TO AXON ADVANCE IN THE AVIAN EMBRYO [J].
OAKLEY, RA ;
TOSNEY, KW .
DEVELOPMENTAL BIOLOGY, 1991, 147 (01) :187-206