MOLECULAR-CLONING OF CDNAS DERIVED FROM A NOVEL HUMAN INTESTINAL MUCIN GENE

被引:385
作者
GUM, JR
HICKS, JW
SWALLOW, DM
LAGACE, RL
BYRD, JC
LAMPORT, DTA
SIDDIKI, B
KIM, YS
机构
[1] VET ADM MED CTR,GASTROINTESTINAL RES LAB 151M2,SAN FRANCISCO,CA 94121
[2] UNIV CALIF SAN FRANCISCO,DEPT MED,SAN FRANCISCO,CA 94143
[3] UNIV LONDON UNIV COLL,MRC,HUMAN BIOCHEM GENET UNIT,LONDON NW1 2HE,ENGLAND
[4] MICHIGAN STATE UNIV,DEPT ENERGY,PLANT RES LAB,E LANSING,MI 48824
[5] MICHIGAN STATE UNIV,DEPT BIOCHEM,E LANSING,MI 48824
关键词
D O I
10.1016/0006-291X(90)91408-K
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
A human small intestianl λgt11 cDNA library was screened with antibodies to deglycosylated small intestianl mucin. Four partial cDNA clones were isolated that define a novel human mucin gene. These include two partial cDNA clones, SIB 124 and SIB 139, that contain 51 nucleotide tandem repeats which encode a seventeen amino acid repetitive peptide with a consensus sequence of HSTPSFTSSITTTETTS. SIB 139 hybridized to messages produced by small intestine, colon, colonic tumors and also by high mucin variant LS174T colon cancer cells. The gene from which cDNAs SIB 124 and SIB 139 are derived (proposed name MUC 3) maps to chromosome 7, distinct from other known human mucin genes. © 1990.
引用
收藏
页码:407 / 415
页数:9
相关论文
共 33 条
[1]  
ALLEN RW, 1987, J BIOL CHEM, V262, P649
[2]  
BURCHELL J, 1983, J IMMUNOL, V131, P508
[3]   DEGLYCOSYLATION OF MUCIN FROM LS174T COLON CANCER-CELLS BY HYDROGEN-FLUORIDE TREATMENT [J].
BYRD, JC ;
LAMPORT, DTA ;
SIDDIQUI, B ;
KUAN, SF ;
ERICKSON, R ;
ITZKOWITZ, SH ;
KIM, YS .
BIOCHEMICAL JOURNAL, 1989, 261 (02) :617-625
[4]  
BYRD JC, 1988, CANCER RES, V48, P6678
[5]   SOMATIC-CELL HYBRIDS BETWEEN MOUSE PERITONEAL MACROPHAGES AND SV40-TRANSFORMED HUMAN CELLS .1. POSITIVE CONTROL OF TRANSFORMED PHENOTYPE BY HUMAN CHROMOSOME-7 CARRYING SV40 GENOME [J].
CROCE, CM ;
KOPROWSKI, H .
JOURNAL OF EXPERIMENTAL MEDICINE, 1974, 140 (05) :1221-1229
[6]  
ECKHARDT AE, 1987, J BIOL CHEM, V262, P11339
[7]   HUMAN MYOSIN HEAVY-CHAIN GENES ASSIGNED TO CHROMOSOME-17 USING A HUMAN CDNA CLONE AS PROBE [J].
EDWARDS, YH ;
PARKAR, M ;
POVEY, S ;
WEST, LF ;
PARRINGTON, JM ;
SOLOMON, E .
ANNALS OF HUMAN GENETICS, 1985, 49 (MAY) :101-109
[8]  
GENDLER S, 1988, J BIOL CHEM, V263, P12820
[9]   CLONING OF PARTIAL CDNA-ENCODING DIFFERENTIATION AND TUMOR-ASSOCIATED MUCIN GLYCOPROTEINS EXPRESSED BY HUMAN MAMMARY EPITHELIUM [J].
GENDLER, SJ ;
BURCHELL, JM ;
DUHIG, T ;
LAMPORT, D ;
WHITE, R ;
PARKER, M ;
TAYLORPAPADIMITRIOU, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (17) :6060-6064
[10]   STUDIES ON THE STRUCTURE OF THE ORGAN-SPECIFIC DETERMINANT OF HUMAN COLONIC MUCIN [J].
GOLD, DV ;
SHOCHAT, D .
MOLECULAR IMMUNOLOGY, 1989, 26 (08) :769-777