Upstream and downstream targets of RUNX proteins

被引:181
作者
Otto, F
Lübbert, M
Stock, M
机构
[1] Univ Freiburg, Med Ctr, Dept Internal Med, Div Haematol & Oncol, D-79106 Freiburg, Germany
[2] Univ Freiburg, Inst Biol 1, D-79106 Freiburg, Germany
关键词
RUNX; transcriptional regulation; transcription factor; AML;
D O I
10.1002/jcb.10491
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
In recent years, the in vivo role of the three members of the RUNX family of transcription factors has in part been elucidated. While Runx1 is essential for mature haematopoiesis and Runx2 for osteochondrogenesis, Runx3 has a function in the nervous system. Translocations and mutations affecting the RUNX1 gene are clearly implicated in leukernogenesis whereas recent data suggest that changed expression levels of RUNX3 may be involved in gastric carcinogenesis. Germ line mutations in RUNX2 have been identified in patients with an autosomal dominant skeletal disorder, cleidocranial dysplasia. While a number of pathways have been delineated that regulate RUNX activity, transcription factors binding to RUNX promoters are only beginning to be identified. A growing number of genes have been characterised that are being regulated in their transcriptional activity by different RUNX proteins. Whether a particular RUNX protein specifically targets a defined subset of downstream genes or whether there is some redundancy as to which RUNX protein activates which target promoter remains to be elucidated. (C) 2003 Wiley-Liss, Inc.
引用
收藏
页码:9 / 18
页数:10
相关论文
共 95 条
[1]   TGF-β-induced repression of CBFA1 by Smad3 decreases cbfa1 and osteocalcin expression and inhibits osteoblast differentiation [J].
Alliston, T ;
Choy, L ;
Ducy, P ;
Karsenty, G ;
Derynck, R .
EMBO JOURNAL, 2001, 20 (09) :2254-2272
[2]   Structural and functional characterization of the human CD36 gene promoter - Identification of a proximal PEBP2/CBF site [J].
Armesilla, AL ;
Calvo, D ;
Vega, MA .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (13) :7781-7787
[3]   An AML-1 consensus sequence binds an osteoblast-specific complex and transcriptionally activates the osteocalcin gene [J].
Banerjee, C ;
Hiebert, SW ;
Stein, JL ;
Lian, JB ;
Stein, GS .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (10) :4968-4973
[4]   Differential regulation of the two principal Runx2/Cbfa1 N-terminal isoforms in response to bone morphogenetic protein-2 during development of the osteoblast phenotype [J].
Banerjee, C ;
Javed, A ;
Choi, JY ;
Green, J ;
Rosen, V ;
van Wijnen, AJ ;
Stein, JL ;
Lian, JB ;
Stein, GS .
ENDOCRINOLOGY, 2001, 142 (09) :4026-4039
[5]   The RUNX3 gene -: sequence, structure and regulated expression [J].
Bangsow, C ;
Rubins, N ;
Glusman, G ;
Bernstein, Y ;
Negreanu, V ;
Goldenberg, D ;
Lotem, J ;
Ben-Asher, E ;
Lancet, D ;
Levanon, D ;
Groner, Y .
GENE, 2001, 279 (02) :221-232
[6]   Core binding factor cannot synergistically activate the myeloperoxidase proximal enhancer in immature myeloid cells without c-Myb [J].
BritosBray, M ;
Friedman, AD .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (09) :5127-5135
[7]   ALY, a context-dependent coactivator of LEF-1 and AML-1, is required for TCR alpha enhancer function [J].
Bruhn, L ;
Munnerlyn, A ;
Grosschedl, R .
GENES & DEVELOPMENT, 1997, 11 (05) :640-653
[8]   Reduction in transforming growth factor β receptor I expression and transcription factor CBFa1 on bone cells by glucocorticoid [J].
Chang, DJ ;
Ji, C ;
Kim, KK ;
Casinghino, S ;
McCarthy, TL ;
Centrella, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (09) :4892-4896
[9]   Physical interaction of the activator protein-1 factors c-Fos and c-Jun with Cbfa1 for collagenase-3 promoter activation [J].
D'Alonzo, RC ;
Selvamurugan, N ;
Karsenty, G ;
Partridge, NC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2002, 277 (01) :816-822
[10]   Role of Cbfa1 in ameloblastin gene transcription [J].
Dhamija, S ;
Krebsbach, PH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2001, 276 (37) :35159-35164