Characterization of the INT6 mammary tumor gene product

被引:18
作者
Diella, F
Levi, G
Callahan, R
机构
[1] NCI,TUMOR IMMUNOL & BIOL LAB,NIH,BETHESDA,MD 20892
[2] ECOLE NORMALE SUPER,INSERM,U368,F-75230 PARIS 05,FRANCE
[3] IST,ADV BIOTECHNOL CTR,UNITA MORFOGENESI MOL,I-16132 GENOA,ITALY
关键词
D O I
10.1089/dna.1997.16.839
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
INT6 is a unique gene, highly conserved throughout evolution and associated with mammary tumorigenesis in the mouse, Although it is expressed in all adult tissues of the mouse and early in embryonic development, its function is unknown, To study the normal distribution and the potential function of the Int6 gene products, we produced antibodies against synthetic peptides specific for the Int6 protein, Western blot and immunoprecipitation analysis demonstrated a 43-kD major gene product that is localized in the cytosolic fraction of mammary cell homogenates, This latter observation is supported by immunoperoxidase analysis, which shows a strong staining anti-Int6 peptide in the perinuclear region of the HC11 mammary epithelial cell line, suggesting a possible localization in the Golgi apparatus, Further immunocytochemical studies in the mouse embryo show that Int6 expression is prevalent in migrating neural crest cells, in the notochord, and in condensing cartilage between 9.5 and 14.5 days of development, In these embryonic tissues, Int6 staining co-localizes with the staining of ricinus lectin, and giantin, proteins that are specifically associated with the Golgi apparatus, The restricted expression of the protein within the Golgi apparatus and its strong conservation throughout evolution suggest that Int6 may perform an essential cellular function.
引用
收藏
页码:839 / 847
页数:9
相关论文
共 27 条
[1]   SUBCELLULAR FATE OF THE INT-2 ONCOPROTEIN IS DETERMINED BY CHOICE OF INITIATION CODON [J].
ACLAND, P ;
DIXON, M ;
PETERS, G ;
DICKSON, C .
NATURE, 1990, 343 (6259) :662-665
[2]  
COLIGAN J, 1991, CURR PROTOCOLS IMMUN, V2
[3]   PROLACTIN AND GLUCOCORTICOID HORMONES SYNERGISTICALLY INDUCE EXPRESSION OF TRANSFECTED RAT BETA-CASEIN GENE PROMOTER CONSTRUCTS IN A MAMMARY EPITHELIAL-CELL LINE [J].
DOPPLER, W ;
GRONER, B ;
BALL, RK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1989, 86 (01) :104-108
[4]   IMMUNOCYTOCHEMICAL LOCALIZATION OF 8 PROTEIN-KINASE-C ISOZYMES OVEREXPRESSED IN NIH 3T3 FIBROBLASTS - ISOFORM-SPECIFIC ASSOCIATION WITH MICROFILAMENTS, GOLGI, ENDOPLASMIC-RETICULUM, AND NUCLEAR AND CELL-MEMBRANES [J].
GOODNIGHT, J ;
MISCHAK, H ;
KOLCH, W ;
MUSHINSKI, JF .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (17) :9991-10001
[5]   INTERNALIZED RICIN AND THE PLASMA-MEMBRANE GLYCOPROTEIN MAM-6 COLOCALIZE IN THE TRANS-GOLGI NETWORK OF T47D HUMAN-BREAST CARCINOMA-CELLS [J].
HANSEN, SH ;
PETERSEN, OW ;
SANDVIG, K ;
OLSNES, S ;
VANDEURS, B .
EXPERIMENTAL CELL RESEARCH, 1989, 185 (02) :373-386
[6]   PROTEIN KINASE-C PHOSPHORYLATION OF THE EGF RECEPTOR AT A THREONINE RESIDUE CLOSE TO THE CYTOPLASMIC FACE OF THE PLASMA-MEMBRANE [J].
HUNTER, T ;
LING, N ;
COOPER, JA .
NATURE, 1984, 311 (5985) :480-483
[7]   IDENTIFICATION OF THE PHOSPHOSERINE RESIDUE IN HISTONE-H1 PHOSPHORYLATED BY PROTEIN KINASE-C [J].
JAKES, S ;
HASTINGS, TG ;
REIMANN, EM ;
SCHLENDER, KK .
FEBS LETTERS, 1988, 234 (01) :31-34
[8]   RETENTION OF FIBROBLAST GROWTH-FACTOR 3 IN THE GOLGI-COMPLEX MAY REGULATE ITS EXPORT FROM CELLS [J].
KIEFER, P ;
PETERS, G ;
DICKSON, C .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (09) :5781-5793
[9]   COMPETITION BETWEEN NUCLEAR-LOCALIZATION AND SECRETORY SIGNALS DETERMINES THE SUBCELLULAR FATE OF A SINGLE CUG-INITIATED FORM OF FGF3 [J].
KIEFER, P ;
ACLAND, P ;
PAPPIN, D ;
PETERS, G ;
DICKSON, C .
EMBO JOURNAL, 1994, 13 (17) :4126-4136
[10]  
KILEY SC, 1995, J CELL SCI, V108, P1003