Cloning and expression analysis of a novel salicylate suppressible gene, Hs-CUL-3, a member of cullin/Cdc53 family

被引:26
作者
Du, M
Sansores-Garcia, L
Zu, ZF
Wu, KKY
机构
[1] Univ Texas, Hlth Sci Ctr, Sch Med, Div Hematol, Houston, TX 77030 USA
[2] Univ Texas, Hlth Sci Ctr, Sch Med, Vasc Biol Res Ctr, Houston, TX 77030 USA
[3] Acad Sinica, Inst Biomed Sci, Vasc Biol Res Program, Taipei 11529, Taiwan
关键词
D O I
10.1074/jbc.273.38.24289
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
By using a mRNA differential display technique to search for salicylate suppressible genes, we identified a cDNA in human foreskin fibroblasts, which by Gen-Bank(TM) DNA data base search shows sequence homology to the recently reported cullin/Cdc53 (CUL) family genes, especially CUL-3, We have cloned the full-length human CUL-3 (Hs-CUL-3) cDNA, It encodes a 768-amino acid polypeptide and has a predicted molecular weight of 88,939, The amino acid sequence of Hs-CUL-3 shows 46% homology to that of its Caenorhabditis elegans ortholog, Ce-CUL-3, and 27 and 23% to that of Hs-CUL-1 and Hs-CUL-2, respectively. Northern blot analysis showed that phorbol 12-myristate 13-acetate increased the expression of Hs-CUL-3 mRNA in a concentration- and time-dependent manner, and this increase was inhibited by sodium salicylate, Hs-CUL-3 widely expressed in human tissues and its expression in cultured COLO205 colon cancer cells was increased when compared with that in normal colon cells, It is Likely that Hs-CUL-3 is involved in cell proliferation control.
引用
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页码:24289 / 24292
页数:4
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共 25 条
[11]  
Mathias N, 1996, MOL CELL BIOL, V16, P6634
[12]   Suppression of intestinal polyposis in Apc(Delta 716) knockout mice by inhibition of cyclooxygenase 2 (COX-2) [J].
Oshima, M ;
Dinchuk, JE ;
Kargman, SL ;
Oshima, H ;
Hancock, B ;
Kwong, E ;
Trzaskos, JM ;
Evans, JF ;
Taketo, MM .
CELL, 1996, 87 (05) :803-809
[13]   The von Hippel-Lindau tumor-suppressor gene product forms a stable complex with human CUL-2, a member of the Cdc53 family of proteins [J].
Pause, A ;
Lee, S ;
Worrell, RA ;
Chen, DYT ;
Burgess, WH ;
Linehan, WM ;
Klausner, RD .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (06) :2156-2161
[14]  
Pierce JW, 1996, J IMMUNOL, V156, P3961
[15]   Activation of p38 mitogen-activated protein kinase by sodium salicylate leads to inhibition of tumor necrosis factor-induced IκBα phosphorylation and degradation [J].
Schwenger, P ;
Alpert, D ;
Skolnik, EY ;
Vilcek, J .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (01) :78-84
[16]   THE B-TYPE CYCLIN KINASE INHIBITOR P40(SIC1) CONTROLS THE G1 TO S TRANSITION IN SACCHAROMYCES-CEREVISIAE [J].
SCHWOB, E ;
BOHM, T ;
MENDENHALL, MD ;
NASMYTH, K .
CELL, 1994, 79 (02) :233-244
[17]   PHARMACOLOGICAL AND BIOCHEMICAL DEMONSTRATION OF THE ROLE OF CYCLOOXYGENASE-2 IN INFLAMMATION AND PAIN [J].
SEIBERT, K ;
ZHANG, Y ;
LEAHY, K ;
HAUSER, S ;
MASFERRER, J ;
PERKINS, W ;
LEE, L ;
ISAKSON, P .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (25) :12013-12017
[18]   Inhibition of human colon cancer cell growth by selective inhibition of cyclooxygenase-2 [J].
Sheng, HM ;
Shao, JY ;
Kirkland, SC ;
Isakson, P ;
Coffey, RJ ;
Morrow, J ;
Beauchamp, RD ;
DuBois, RN .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 99 (09) :2254-2259
[19]   F-box proteins are receptors that recruit phosphorylated substrates to the SCF ubiquitin-ligase complex [J].
Skowyra, D ;
Craig, KL ;
Tyers, M ;
Elledge, SJ ;
Harper, JW .
CELL, 1997, 91 (02) :209-219
[20]   INHIBITION OF PROSTAGLANDIN SYNTHESIS AS A MECHANISM OF ACTION FOR ASPIRIN-LIKE DRUGS [J].
VANE, JR .
NATURE-NEW BIOLOGY, 1971, 231 (25) :232-&