THE ISOLATION AND CHARACTERIZATION OF A NOVEL CDNA DEMONSTRATING AN ALTERED MESSENGER-RNA LEVEL IN NONTUMORIGENIC WILMS MICROCELL HYBRID-CELLS

被引:113
作者
DOWDY, SF
LAI, KM
WEISSMAN, BE
MATSUI, Y
HOGAN, BLM
STANBRIDGE, EJ
机构
[1] UNIV CALIF IRVINE,SCH MED,DEPT MICROBIOL & MOLEC GENET,IRVINE,CA 92717
[2] UNIV N CAROLINA,LINEBURGER CANC RES CTR,CHAPEL HILL,NC 27516
[3] VANDERBILT UNIV,MED CTR,SCH MED,DEPT CELL BIOL,NASHVILLE,TN 37232
关键词
D O I
10.1093/nar/19.20.5763
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
Wilms' tumor, a pediatric nephroblastoma, has been associated with genetic alterations of the 11p13 and 11p15 regions. The introduction of a der(11) chromosome into the G401 Wilms' tumor cell line has been shown previously to revert the tumorigenic phenotype. A subtractive cDNA/RNA hybridization performed between the tumorigenic parent (G401) and a nontumorigenic microcell hybrid of G401 (110.1/G401.1) containing the der(11) chromosome resulted in the identification of a single novel cDNA clone, designated QM. The cDNA is 745 nucleotides in length and encodes a predicted hydrophilic 25 kd basic protein, primarily consisting of alpha helices. The QM transcript is expressed in a wide variety of embryonic and adult tissues and demonstrates a down regulation of expression in adult kidney and heart. QM is also a member of a multigene family members of which map to chromosomes 6 and 14. The QM mRNA level is modulated between the tumorigenic and nontumorigenic cell lines and therefore may be involved in the maintenance of the nontumorigenic phenotype.
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页码:5763 / 5769
页数:7
相关论文
共 36 条
[1]   WILMS TUMOR AND OTHER RENAL TUMORS OF CHILDHOOD - A SELECTIVE REVIEW FROM THE NATIONAL-WILMS-TUMOR-STUDY-PATHOLOGY-CENTER [J].
BECKWITH, JB .
HUMAN PATHOLOGY, 1983, 14 (06) :481-492
[2]   VIRAL ONCOGENES [J].
BISHOP, JM .
CELL, 1985, 42 (01) :23-38
[3]   ISOLATION AND CHARACTERIZATION OF A ZINC FINGER POLYPEPTIDE GENE AT THE HUMAN CHROMOSOME-11 WILMS TUMOR LOCUS [J].
CALL, KM ;
GLASER, T ;
ITO, CY ;
BUCKLER, AJ ;
PELLETIER, J ;
HABER, DA ;
ROSE, EA ;
KRAL, A ;
YEGER, H ;
LEWIS, WH ;
JONES, C ;
HOUSMAN, DE .
CELL, 1990, 60 (03) :509-520
[4]   PREDICTION OF PROTEIN CONFORMATION [J].
CHOU, PY ;
FASMAN, GD .
BIOCHEMISTRY, 1974, 13 (02) :222-245
[5]   CELL-TYPE-SPECIFIC CDNA PROBES AND THE MURINE-I REGION - THE LOCALIZATION AND ORIENTATION OF A-ALPHA-D [J].
DAVIS, MM ;
COHEN, DI ;
NIELSEN, EA ;
STEINMETZ, M ;
PAUL, WE ;
HOOD, L .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (07) :2194-2198
[6]   EXPRESSION OF A SINGLE TRANSFECTED CDNA CONVERTS FIBROBLASTS TO MYOBLASTS [J].
DAVIS, RL ;
WEINTRAUB, H ;
LASSAR, AB .
CELL, 1987, 51 (06) :987-1000
[7]  
DOWDY SF, 1991, IN PRESS SCIENCE
[8]   USE OF A CLONED LIBRARY FOR THE STUDY OF ABUNDANT POLY(A)+RNA DURING XENOPUS-LAEVIS DEVELOPMENT [J].
DWORKIN, MB ;
DAWID, IB .
DEVELOPMENTAL BIOLOGY, 1980, 76 (02) :449-464
[9]  
FEINBERG AP, 1984, ANAL BIOCHEM, V132, P6
[10]  
FOURNIER REK, 1977, P NATL ACAD SCI USA, V74, P456