THE HUMAN TYROSINE KINASE GENE (FER) MAPS TO CHROMOSOME-5 AND IS DELETED IN MYELOID LEUKEMIAS WITH A DEL(5Q)

被引:25
作者
MORRIS, C
HEISTERKAMP, N
HAO, QL
TESTA, JR
GROFFEN, J
机构
[1] CHILDRENS HOSP LOS ANGELES,DEPT PATHOL,MOLEC DIAGNOSIS SECT,4650 SUNSET BLVD,LOS ANGELES,CA 90027
[2] UNIV MARYLAND,CTR CANC,BALTIMORE,MD 21201
来源
CYTOGENETICS AND CELL GENETICS | 1990年 / 53卷 / 04期
关键词
D O I
10.1159/000132929
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
A novel member of the SRC tyrosine kinase gene family was recently isolated and characterized (Hao et al., 1989). This FES/FPS-related gene, named FER. lacks the transmembrane and extracellular domains which characterize tyrosine kinases with receptor function. Expression of FER in a wide range of cell types indicates a general role in intracellular signalling or differentiation processes. We have now mapped FER to chromosome 5ql4→q23 using in situ hybridization techniques and suggest a more precise location within bands 5q21→ q22. This region lies adjacent to a complex domain of growth factors and receptors. many involved in regulation of haematopoiesis. FER maps within a critical segment frequently deleted from chromosome 5 in patients with acute myeloid leukemia or myelodysplastic syndromes and was shown to be deleted in two such patients. It also maps close to the familial polyposis coli locus at 5q22. © 1990 S. Karger AG, Basel.
引用
收藏
页码:196 / 200
页数:5
相关论文
共 41 条
[1]  
BARTRAM CR, 1987, LEUKEMIA, V1, P146
[2]   VIRAL ONCOGENES [J].
BISHOP, JM .
CELL, 1985, 42 (01) :23-38
[3]   LOCALIZATION OF THE GENE FOR FAMILIAL ADENOMATOUS POLYPOSIS ON CHROMOSOME-5 [J].
BODMER, WF ;
BAILEY, CJ ;
BODMER, J ;
BUSSEY, HJR ;
ELLIS, A ;
GORMAN, P ;
LUCIBELLO, FC ;
MURDAY, VA ;
RIDER, SH ;
SCAMBLER, P ;
SHEER, D ;
SOLOMON, E ;
SPURR, NK .
NATURE, 1987, 328 (6131) :614-616
[4]   AN IMPROVED METHOD FOR G-BANDING CHROMOSOMES AFTER INSITU HYBRIDIZATION [J].
CANNIZZARO, LA ;
EMANUEL, BS .
CYTOGENETICS AND CELL GENETICS, 1984, 38 (04) :308-309
[5]   EXPRESSION OF RECESSIVE ALLELES BY CHROMOSOMAL MECHANISMS IN RETINOBLASTOMA [J].
CAVENEE, WK ;
DRYJA, TP ;
PHILLIPS, RA ;
BENEDICT, WF ;
GODBOUT, R ;
GALLIE, BL ;
MURPHREE, AL ;
STRONG, LC ;
WHITE, RL .
NATURE, 1983, 305 (5937) :779-784
[6]   ANTIPEPTIDE ANTISERUM IDENTIFIES A WIDELY DISTRIBUTED CELLULAR TYROSINE KINASE RELATED TO BUT DISTINCT FROM THE C-FPS FES-ENCODED PROTEIN [J].
FELDMAN, RA ;
TAM, JP ;
HANAFUSA, H .
MOLECULAR AND CELLULAR BIOLOGY, 1986, 6 (04) :1065-1073
[7]   THE CD14 MONOCYTE DIFFERENTIATION ANTIGEN MAPS TO A REGION ENCODING GROWTH-FACTORS AND RECEPTORS [J].
GOYERT, SM ;
FERRERO, E ;
RETTIG, WJ ;
YENAMANDRA, AK ;
OBATA, F ;
LEBEAU, MM .
SCIENCE, 1988, 239 (4839) :497-500
[8]   HOMOLOGY BETWEEN PHOSPHOTYROSINE ACCEPTOR SITE OF HUMAN C-ABL AND VIRAL ONCOGENE PRODUCTS [J].
GROFFEN, J ;
HEISTERKAMP, N ;
REYNOLDS, FH ;
STEPHENSON, JR .
NATURE, 1983, 304 (5922) :167-169
[9]   CHROMOSOMAL LOCALIZATION OF THE HUMAN C-FMS ONCOGENE [J].
GROFFEN, J ;
HEISTERKAMP, N ;
SPURR, N ;
DANA, S ;
WASMUTH, JJ ;
STEPHENSON, JR .
NUCLEIC ACIDS RESEARCH, 1983, 11 (18) :6331-6339
[10]   ISOLATION AND SEQUENCE-ANALYSIS OF A NOVEL HUMAN TYROSINE KINASE GENE [J].
HAO, QL ;
HEISTERKAMP, N ;
GROFFEN, J .
MOLECULAR AND CELLULAR BIOLOGY, 1989, 9 (04) :1587-1593