A novel gene family encoding leucine-rich repeat transmembrane proteins differentially expressed in the nervous system

被引:120
作者
Laurén, J [1 ]
Airaksinen, MS [1 ]
Saarma, M [1 ]
Timmusk, T [1 ]
机构
[1] Univ Helsinki, Inst Biotechnol, Program Mol Neurobiol, FIN-00014 Helsinki, Finland
基金
芬兰科学院;
关键词
leucine-rich repeat; transmembrane protein; cell adhesion; cell signaling; receptor; neuron; nervous system; catenin;
D O I
10.1016/S0888-7543(03)00030-2
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
Leucine-rich repeat containing proteins are involved in protein-protein interactions and they regulate numerous cellular events during nervous system development and disease. Here we have isolated and characterized a new four-membered family of genes from human and mouse, named LRRTMs, that encode putative leucine-rich repeat transmembrane proteins. Human and mouse LRRTMs are highly conserved, and orthologous genes exist in other vertebrates but not in invertebrates. All LRRTMs, except LRRTM4, are located in the introns of different a-catenin genes, suggesting coevolution of these two gene families. We show by in situ hybridization and RT-PCR that LRRTM mRNAs are predominantly expressed in the nervous system and that each LRRTM possesses a specific, partially nonoverlapping expression pattern. The structure and expression profile of LRRTM mRNAs suggest that they may have a role in the development and maintenance of the vertebrate nervous system. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:411 / 421
页数:11
相关论文
共 21 条
[1]   GAC1, a new member of the leucine-rich repeat superfamily on chromosome band 1q32.1, is amplified and overexpressed in malignant gliomas [J].
Almeida, A ;
Zhu, XX ;
Vogt, N ;
Tyagi, R ;
Muleris, M ;
Dutrillaux, AM ;
Dutrillaux, B ;
Ross, D ;
Malfoy, B ;
Hanash, S .
ONCOGENE, 1998, 16 (23) :2997-3002
[2]   The lutropin/choriocrctnadotropin receptor, a 2002 perspective [J].
Ascoli, M ;
Fanelli, F ;
Segaloff, DL .
ENDOCRINE REVIEWS, 2002, 23 (02) :141-174
[3]   Mutations in NYX, encoding the leucine-rich proteoglycan nyctalopin, cause X-linked complete congenital stationary night blindness [J].
Bech-Hansen, NT ;
Naylor, MJ ;
Maybaum, TA ;
Sparkes, RL ;
Koop, B ;
Birch, DG ;
Bergen, AAB ;
Prinsen, CFM ;
Polomeno, RC ;
Gal, A ;
Drack, AV ;
Musarella, MA ;
Jacobson, SG ;
Young, RSL ;
Weleber, RG .
NATURE GENETICS, 2000, 26 (03) :319-323
[4]   Molecules, maps and synapse specificity [J].
Benson, DL ;
Colman, DR ;
Huntley, GW .
NATURE REVIEWS NEUROSCIENCE, 2001, 2 (12) :899-909
[5]   Identification of a receptor mediating Nogo-66 inhibition of axonal regeneration [J].
Fournier, AE ;
GrandPre, T ;
Strittmatter, SM .
NATURE, 2001, 409 (6818) :341-346
[6]   Structures of glycoprotein Ibα and its complex with von Willebrand factor A1 domain [J].
Huizinga, EG ;
Tsuji, S ;
Romijn, RAP ;
Schiphorst, ME ;
de Groot, PG ;
Sixma, JJ ;
Gros, P .
SCIENCE, 2002, 297 (5584) :1176-1179
[7]   PDZ domains: Structural modules for protein complex assembly [J].
Hung, AY ;
Sheng, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (08) :5699-5702
[8]   Structural diversity of leucine-rich repeat proteins [J].
Kajava, AV .
JOURNAL OF MOLECULAR BIOLOGY, 1998, 277 (03) :519-527
[9]   Mutations in LGI1 cause autosomal-dominant partial epilepsy with auditory features [J].
Kalachikov, S ;
Evgrafov, O ;
Ross, B ;
Winawer, M ;
Barker-Cummings, C ;
Boneschi, FM ;
Choi, C ;
Morozov, P ;
Das, K ;
Teplitskaya, E ;
Yu, A ;
Cayanis, E ;
Penchaszadeh, G ;
Kottmann, AH ;
Pedley, TA ;
Hauser, WA ;
Ottman, R ;
Gilliam, TC .
NATURE GENETICS, 2002, 30 (03) :335-341
[10]   The leucine-rich repeat as a protein recognition motif [J].
Kobe, B ;
Kajava, AV .
CURRENT OPINION IN STRUCTURAL BIOLOGY, 2001, 11 (06) :725-732