Homologs of RUNX and CBFβ/PEBP2β in C-elegans

被引:22
作者
Lee, J
Ahnn, J
Bae, SC
机构
[1] Yonsei Univ, Dept Biol, Natl Res Lab, Seoul 120749, South Korea
[2] Kwangju Inst Sci & Technol, Dept Life Sci, Kwangju 500712, South Korea
[3] Chungbuk Natl Univ, Coll Med, Dept Biochem, Tumor Res Ctr, Cheongju 361763, South Korea
关键词
C; elegans; RUNX; BRO-1; evolution; TGF-beta;
D O I
10.1038/sj.onc.1207669
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
RUNX proteins are evolutionarily well-conserved transcription factors that are involved in essential aspects of the development of metazoan animals ranging from nematodes to humans. Geneticor epigenetic defects in any one of the three RUNX proteins in humans cause severe diseases. Although much is known about the functions and signaling pathways of the RUNX proteins through the use of mammalian systems, there are still gaps in our knowledge with regard to the functions of the RUNX proteins in normal development and disease states. Recently, the nematode Caenorhabditis elegans was revealed to bear one RUNX homolog (RNT-1) and one homolog of the RUNX protein partner CBFbeta/PEBP2beta (BRO-1). The expression patterns and biological functions of RNT-1 and the manner in which it is regulated are all comparable to what has been observed for the mammalian RUNX proteins. Thus, the nematode system is a promising model system for elucidating the functions and regulation of Runt proteins. In addition, it has recently emerged that the RNT-1 protein is involved in a transforming growth factor beta signaling pathway. The bro-1 gene encoding the CBFbeta homolog is exclusively expressed in the hypodermis, not in the intestine, which indicates that additional tissue-specific cofactors in the intestine might exist. The possible autoregulation of RNT1 expression by RNT-1/BRO-1 in the hypodermal cells is also discussed.
引用
收藏
页码:4346 / 4352
页数:7
相关论文
共 56 条
[1]  
[Anonymous], 1998, SCIENCE, V282, P2012
[2]   THE LET-23 GENE NECESSARY FOR CAENORHABDITIS-ELEGANS VULVAR INDUCTION ENCODES A TYROSINE KINASE OF THE EGF RECEPTOR SUBFAMILY [J].
AROIAN, RV ;
KOGA, M ;
MENDEL, JE ;
OHSHIMA, Y ;
STERNBERG, PW .
NATURE, 1990, 348 (6303) :693-699
[3]   Groucho-dependent and -independent repression activities of runt domain proteins [J].
Aronson, BD ;
Fisher, AL ;
Blechman, K ;
Caudy, M ;
Gergen, JP .
MOLECULAR AND CELLULAR BIOLOGY, 1997, 17 (09) :5581-5587
[4]  
BAE SC, 1993, ONCOGENE, V8, P809
[5]   CLONING, MAPPING AND EXPRESSION OF PEBP2-ALPHA-C, A 3RD GENE ENCODING THE MAMMALIAN RUNT DOMAIN [J].
BAE, SC ;
TAKAHASHI, E ;
ZHANG, YW ;
OGAWA, E ;
SHIGESADA, K ;
NAMBA, Y ;
SATAKE, M ;
ITO, Y .
GENE, 1995, 159 (02) :245-248
[6]   cDNA cloning of run, a Caenorhabditis elegans Runt domain encoding gene [J].
Bae, SC ;
Lee, J .
GENE, 2000, 241 (02) :255-258
[7]  
BOWTELL DDL, 1995, ONCOGENE, V11, P1561
[8]  
BRENNER S, 1974, GENETICS, V77, P71
[9]   The proto-oncogene c-Cbl is a negative regulator of DNA synthesis initiated by both receptor and cytoplasmic tyrosine kinases [J].
Broome, MA ;
Galisteo, ML ;
Schlessinger, J ;
Courtneidge, SA .
ONCOGENE, 1999, 18 (18) :2908-2912
[10]   Runx transcription factors and the developmental balance between cell proliferation and differentiation [J].
Coffman, JA .
CELL BIOLOGY INTERNATIONAL, 2003, 27 (04) :315-324