ATRA-regulated Asb-2 gene induced in differentiation of HL-60 leukemia cells

被引:54
作者
Kohroki, J
Fujita, S
Itoh, N
Yamada, Y
Imai, H
Yumoto, N
Nakanishi, T
Tanaka, K
机构
[1] Osaka Univ, Grad Sch Pharmaceut Sci, Suita, Osaka 5650871, Japan
[2] Natl Inst Adv Ind Sci & Technol, Osaka 5638577, Japan
关键词
ASB-2; all-trans retinoic acid; retinoid receptor alpha; leukemia; differentiation;
D O I
10.1016/S0014-5793(01)02829-0
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
Suppressors of cytokine signaling (SOCS) proteins possess common structures, a SOCS box at the C-terminus and a SH2 domain at their center. These suppressors are inducible in response to cytokines and act as negative regulators of cytokine signaling. The ASB proteins also contain the SOCS box and the ankyrin repeat sequence at the N-terminus, but do not have the SH2 domain. Although Socs genes are directly induced by several cytokines, no Asb gene inducers have been identified. In this study, we screened the specific genes expressed in the course of differentiation of HL-60 cells, and demonstrated that ASB-2, one of the ASB proteins, was rapidly induced by all-trans retinoic acid (ATRA). Typical retinoid receptors (RA Rs) or retinoid X receptors (RXRs) binding element (RARE/RXRE) were presented in the promoter of the Asb-2 gene. We showed that RAR alpha, one of the RARs, binds to the RARE/RXRE in the Asb-2 promoter. In addition, we demonstrated by luciferase reporter assay that this element was a functional RARE/RXRE. These findings indicate that ASB-2 is directly induced by ATRA and may act as a significant regulator, underlying such physiological processes as cell differentiation. (C) 2001 Federation of European Biochemical Societies. Published by Elsevier Science B.V. All rights reserved.
引用
收藏
页码:223 / 228
页数:6
相关论文
共 29 条
[1]   INDUCTION OF DIFFERENTIATION OF THE HUMAN PROMYELOCYTIC LEUKEMIA-CELL LINE (HL-60) BY RETINOIC ACID [J].
BREITMAN, TR ;
SELONICK, SE ;
COLLINS, SJ .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1980, 77 (05) :2936-2940
[2]  
DAWSON MI, 1994, BLOOD, V84, P446
[3]   A new protein containing an SH2 domain that inhibits JAK kinases [J].
Endo, TA ;
Masuhara, M ;
Yokouchi, M ;
Suzuki, R ;
Sakamoto, H ;
Mitsui, K ;
Matsumoto, A ;
Tanimura, S ;
Ohtsubo, M ;
Misawa, H ;
Miyazaki, T ;
Leonor, N ;
Taniguchi, T ;
Fujita, T ;
Kanakura, Y ;
Komiya, S ;
Yoshimura, A .
NATURE, 1997, 387 (6636) :921-924
[4]   Socs-1 inhibits TEL-JAK2-mediated transformation of hematopoietic cells through inhibition of JAK2 kinase activity and induction of proteasome-mediated degradation [J].
Frantsve, J ;
Schwaller, J ;
Sternberg, DW ;
Kutok, J ;
Gilliland, DG .
MOLECULAR AND CELLULAR BIOLOGY, 2001, 21 (10) :3547-3557
[5]  
GRATAS C, 1993, LEUKEMIA, V7, P1156
[6]   Distinct interactions of PML-RARα and PLZF-RARα with co-repressors determine differential responses to RA in APL [J].
He, LZ ;
Guidez, F ;
Tribioli, C ;
Peruzzi, D ;
Ruthardt, M ;
Zelent, A ;
Pandolfi, PP .
NATURE GENETICS, 1998, 18 (02) :126-135
[7]   Twenty proteins containing a C-terminal SOCS box form five structural classes [J].
Hilton, DJ ;
Richardson, RT ;
Alexander, WS ;
Viney, EM ;
Willson, TA ;
Sprigg, NS ;
Starr, R ;
Nicholson, SE ;
Metcalf, D ;
Nicola, NA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (01) :114-119
[8]   The SOCS box of SOCS-1 accelerates ubiquitin-dependent proteolysis of TEL-JAK2 [J].
Kamizono, S ;
Hanada, T ;
Yasukawa, H ;
Minoguchi, S ;
Kato, R ;
Minoguchi, M ;
Hattori, K ;
Hatakeyama, S ;
Yada, M ;
Morita, S ;
Kitamura, T ;
Kato, H ;
Nakayama, K ;
Yoshimura, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (16) :12530-12538
[9]   Rbx1, a component of the VHL tumor suppressor complex and SCF ubiquitin ligase [J].
Kamura, T ;
Koepp, DM ;
Conrad, MN ;
Skowyra, D ;
Moreland, RJ ;
Iliopoulos, O ;
Lane, WS ;
Kaelin, WG ;
Elledge, SJ ;
Conaway, RC ;
Harper, JW ;
Conway, JW .
SCIENCE, 1999, 284 (5414) :657-661
[10]   The Elongin BC complex interacts with the conserved SOCS-box motif present in members of the SOCS, ras, WD-40 repeat, and ankyrin repeat families [J].
Kamura, T ;
Sato, S ;
Haque, D ;
Liu, L ;
Kaelin, WG ;
Conaway, RC ;
Conaway, JW .
GENES & DEVELOPMENT, 1998, 12 (24) :3872-3881