Cloning and identification of a cDNA that encodes a novel human protein with thrombospondin type I repeat domain, hPWTSR

被引:40
作者
Chen, JZ
Wang, S
Tang, R
Yang, QS
Zhao, EP
Chao, YQ
Ying, K
Xie, Y
Mao, YM [1 ]
机构
[1] Fudan Univ, Sch Life Sci, State Key Lab Genet Engn, Shanghai 200433, Peoples R China
[2] United Gene Holdings Ltd, Shanghai 200092, Peoples R China
关键词
cysteine-rich region; hPWTSR; thrombospondin (TSP); thrombospondin type I repeat (TSR);
D O I
10.1023/A:1020479301379
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 cDNA was isolated from the fetal brain cDNA library by high throughput cDNA sequencing. The 2390 bp cDNA with an open reading fragment (ORF) of 816 bp encodes a 272 amino acids putative protein with a thrombospondin type 1 repeat (TSR) domain and a cysteine-rich region at the N-terminus, so it is named hPWTSR. We used Northern blot detected two bands with length of about 3 kb and 4 kb respectively, which expressed in human adult tissues with different intensities. The expression pattern was verified by RT-PCR, revealing that the transcripts were expressed ubiquitously in fetal tissues and human tumor tissues too. However, the transcript was detected neither in ovarian carcinoma GI-102 nor in lung carcinoma LX-1. Blast analysis against NCBI database revealed that the new gene contained at least 5 exons and located in human chromosome 6q22.33. Our results demonstrate that the gene is a novel member of TSR supergene family.
引用
收藏
页码:287 / 292
页数:6
相关论文
共 17 条
[1]  
Adams JC, 2000, DEV DYNAM, V218, P280
[2]   Thrombospondin type 1 repeats interact with matrix metalloproteinase 2 - Regulation of metalloproteinase activity [J].
Bein, K ;
Simons, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2000, 275 (41) :32167-32173
[3]  
BORNSTEIN P, 1994, METHOD ENZYMOL, V245, P62
[4]   The cell biology of thrombospondin-1 [J].
Chen, H ;
Herndon, ME ;
Lawler, J .
MATRIX BIOLOGY, 2000, 19 (07) :597-614
[5]   Thrombospondin-1 is a major activator of TGF-β1 in vivo [J].
Crawford, SE ;
Stellmach, V ;
Murphy-Ullrich, JE ;
Ribeiro, SMF ;
Lawler, J ;
Hynes, RO ;
Boivin, GP ;
Bouck, N .
CELL, 1998, 93 (07) :1159-1170
[6]   Thrombospondins and tumor angiogenesis [J].
de Fraipont, F ;
Nicholson, AC ;
Feige, JJ ;
Van Meir, EG .
TRENDS IN MOLECULAR MEDICINE, 2001, 7 (09) :401-407
[7]  
Feinstein Y, 1999, DEVELOPMENT, V126, P3637
[8]  
HYNES RO, 1986, J CELL BIOL, V103, P1635
[9]   Mice that lack thrombospondin 2 display connective tissue abnormalities that are associated with disordered collagen fibrillogenesis, an increased vascular density, and a bleeding diathesis [J].
Kyriakides, TR ;
Zhu, YH ;
Smith, LT ;
Bain, SD ;
Yang, ZT ;
Lin, MT ;
Danielson, KG ;
Iozzo, RV ;
LaMarca, M ;
McKinney, CE ;
Ginns, EI ;
Bornstein, P .
JOURNAL OF CELL BIOLOGY, 1998, 140 (02) :419-430
[10]   Mice that lack the angiogenesis inhibitor, thrombospondin 2, mount an altered foreign body reaction characterized by increased vascularity [J].
Kyriakides, TR ;
Leach, KJ ;
Hoffman, AS ;
Ratner, BD ;
Bornstein, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1999, 96 (08) :4449-4454