IDENTIFICATION OF THE NEUROFIBROMATOSIS TYPE-1 GENE-PRODUCT

被引:232
作者
GUTMANN, DH
WOOD, DL
COLLINS, FS
机构
[1] UNIV MICHIGAN,DEPT INTERNAL MED,ANN ARBOR,MI 48109
[2] UNIV MICHIGAN,DEPT HUMAN GENET,ANN ARBOR,MI 48109
[3] UNIV MICHIGAN,HOWARD HUGHES MED INST,ANN ARBOR,MI 48109
关键词
PROTEIN; ANTIBODIES; GTPASE-ACTIVATING PROTEIN;
D O I
10.1073/pnas.88.21.9658
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The gene for neurofibromatosis type 1 (NF1) was recently identified by positional cloning. The complete cDNA encodes a polypeptide of 2818 amino acids. To study the NF1 gene product, antibodies were raised against both fusion proteins and synthetic peptides. Initial characterization of two anti-peptide antibodies and one fusion-protein antibody demonstrated a specific protein of almost-equal-to 250 kDa by both immunoprecipitation and immunoblotting. This protein was found in all tissues and cell lines examined and is detected in human, rat, and mouse tissues. To demonstrate that these antibodies specifically recognize the NF1 protein, additional fusion proteins containing the sequence specific to the synthetic peptide were generated. Both peptide antisera recognize the proper specific fusion proteins so generated. Immunoprecipitates using the peptide antisera were shown to recognize the same protein detected by immunoblotting with either the other peptide antiserum or the fusion-protein antiserum. Immunoblotting using antiserum specific to spatially distinct epitopes conducted on tissue homogenates demonstrated the NF1 protein in all adult tissues. Based on the homology between the NF1 gene product and members of the GTPase-activating protein (GAP) superfamily, the name NF1-GAP-related protein (NF1GRP) is suggested.
引用
收藏
页码:9658 / 9662
页数:5
相关论文
共 28 条
  • [1] THE NF1 LOCUS ENCODES A PROTEIN FUNCTIONALLY RELATED TO MAMMALIAN GAP AND YEAST IRA PROTEINS
    BALLESTER, R
    MARCHUK, D
    BOGUSKI, M
    SAULINO, A
    LETCHER, R
    WIGLER, M
    COLLINS, F
    [J]. CELL, 1990, 63 (04) : 851 - 859
  • [2] DUCHENNE MUSCULAR-DYSTROPHY - DEFICIENCY OF DYSTROPHIN AT THE MUSCLE-CELL SURFACE
    BONILLA, E
    SAMITT, CE
    MIRANDA, AF
    HAYS, AP
    SALVIATI, G
    DIMAURO, S
    KUNKEL, LM
    HOFFMAN, EP
    ROWLAND, LP
    [J]. CELL, 1988, 54 (04) : 447 - 452
  • [3] BOULTONT G, 1991, CELL, V65, P663
  • [4] SEQUENCE HOMOLOGY SHARED BY NEUROFIBROMATOSIS TYPE-1 GENE AND IRA-1 AND IRA-2 NEGATIVE REGULATORS OF THE RAS CYCLIC-AMP PATHWAY
    BUCHBERG, AM
    CLEVELAND, LS
    JENKINS, NA
    COPELAND, NG
    [J]. NATURE, 1990, 347 (6290) : 291 - 294
  • [5] A MAJOR SEGMENT OF THE NEUROFIBROMATOSIS TYPE-1 GENE - CDNA SEQUENCE, GENOMIC STRUCTURE, AND POINT MUTATIONS
    CAWTHON, RM
    WEISS, R
    XU, GF
    VISKOCHIL, D
    CULVER, M
    STEVENS, J
    ROBERTSON, M
    DUNN, D
    GESTELAND, R
    OCONNELL, P
    WHITE, R
    [J]. CELL, 1990, 62 (01) : 193 - 201
  • [6] GOLDGAR DE, 1989, AM J HUM GENET, V44, P6
  • [7] RAS AND GAP - WHOS CONTROLLING WHOM
    HALL, A
    [J]. CELL, 1990, 61 (06) : 921 - 923
  • [8] HARLOW E, 1988, ANTIBODIES LABORATOR, P421
  • [9] HIGH-AFFINITY NGF BINDING REQUIRES COEXPRESSION OF THE TRK PROTOONCOGENE AND THE LOW-AFFINITY NGF RECEPTOR
    HEMPSTEAD, BL
    MARTINZANCA, D
    KAPLAN, DR
    PARADA, LF
    CHAO, MV
    [J]. NATURE, 1991, 350 (6320) : 678 - 683
  • [10] DYSTROPHIN - THE PROTEIN PRODUCT OF THE DUCHENNE MUSCULAR-DYSTROPHY LOCUS
    HOFFMAN, EP
    BROWN, RH
    KUNKEL, LM
    [J]. CELL, 1987, 51 (06) : 919 - 928