ISOLATION AND CHARACTERIZATION OF A ZINC FINGER POLYPEPTIDE GENE AT THE HUMAN CHROMOSOME-11 WILMS TUMOR LOCUS

被引:1770
作者
CALL, KM
GLASER, T
ITO, CY
BUCKLER, AJ
PELLETIER, J
HABER, DA
ROSE, EA
KRAL, A
YEGER, H
LEWIS, WH
JONES, C
HOUSMAN, DE
机构
[1] HARVARD UNIV,SCH MED,DANA FARBER CANC INST,DIV MED ONCOL,BOSTON,MA 02115
[2] HOSP SICK CHILDREN,RES INST,DEPT PATHOL,TORONTO M5S 1A8,ONTARIO,CANADA
[3] UNIV TORONTO,DEPT MICROBIOL,TORONTO M4X 1K9,ONTARIO,CANADA
[4] ELEANOR ROOSEVELT INST CANC RES,DEPT BIOCHEM,DENVER,CO 80262
[5] UNIV COLORADO,HLTH SCI CTR,DENVER,CO 80262
关键词
D O I
10.1016/0092-8674(90)90601-A
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
We have isolated a series of genomic and cDNA clones mapping within the boundaries of constitutional and tumor deletions that define the Wilms' tumor locus on human chromsome 11 (band p13). The transcription unit corresponding to these clones spans approximately 50 kb and encodes an mRNA approximately 3 kb long. This mRNA is expressed in a limited range of cell types, predominantly in the kidney and a subset of hematopoietic cells. The polypeptide encoded by this locus has a number of features suggesting a potential role in transcriptional regulation. These include the presence of four zinc finger domains and a region rich in proline and glutamine. The amino acid sequence of the predicted polypeptide shows significant homology to two growth regulated mammalian polypeptides, EGR1 and EGR2. The genetic localization of this gene, its tissue-specific expression, and the function predicted from its sequence lead us to suggest that it represents the 11p13 Wilms' tumor gene. © 1990.
引用
收藏
页码:509 / 520
页数:12
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