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Human Hrs, a tyrosine kinase substrate in growth factor-stimulated cells: cDNA cloning and mapping of the gene to chromosome 17
被引:8
|作者:
Lu, LG
Komada, M
Kitamura, N
[1
]
机构:
[1] Tokyo Inst Technol, Fac Biosci & Biotechnol, Dept Life Sci, Midori Ku, Yokohama, Kanagawa 226, Japan
[2] Kansai Med Univ, Inst Liver Res, Moriguchi, Osaka 570, Japan
来源:
关键词:
HGF;
scatter factor;
tyrosine phosphorylation;
zinc finger;
early endosome;
D O I:
10.1016/S0378-1119(98)00184-X
中图分类号:
Q3 [遗传学];
学科分类号:
071007 ;
090102 ;
摘要:
Hrs is a 115 kDa zinc finger protein which is rapidly tyrosine phosphorylated in cells stimulated with various growth factors. We previously purified the protein from a mouse cell line and cloned its cDNA. In the present study, we cloned a human Hrs cDNA from a human placenta cDNA library by cross-hybridization, using the mouse cDNA as a probe, and determined its nucleotide sequence. The human Hrs cDNA encoded a 777-amino-acid protein whose sequence was 93% identical to that of mouse Hrs. Northern blot analysis showed that the Hrs mRNA was about 3.0 kb long and was expressed in all the human adult and fetal tissues tested. In addition, we showed by genomic Southern blot analysis that the human Hrs gene was a single-copy gene with a size of about 20 kb. Furthermore, the human Hrs gene was mapped to chromosome 17 by Southern blotting of genomic DNAs from human/rodent somatic cell hybrids. (C) 1998 Elsevier Science B.V. All rights reserved.
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页码:125 / 132
页数:8
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