C. elegans twist gene expression in differentiated cell types is controlled by autoregulation through intron elements

被引:11
作者
Meyers, Stephany G. [1 ]
Corsi, Ann K. [1 ]
机构
[1] Catholic Univ Amer, Dept Biol, Washington, DC 20064 USA
基金
美国国家卫生研究院;
关键词
Twist; Mesoderm; C; elegans; Intron elements; E box; hlh-8; bHLH transcription factor; Autoregulation; hlh-8 (tm726); E/DAUGHTERLESS ORTHOLOG HLH-2; CAENORHABDITIS-ELEGANS; MUSCLE; PROTEIN; TARGET; IDENTIFICATION; HOMOLOG; ROLES; PLAYS;
D O I
10.1016/j.ydbio.2010.07.025
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The temporospatial regulation of genes encoding transcription factors is important during development. The hlh-8 gene encodes the C elegans mesodermal transcription factor CeTwist. Elements in the hlh-8 promoter restrict gene expression to predominantly undifferentiated cells of the M lineage. We have discovered that hlh-8 expression in differentiated mesodermal cells is controlled by two well-conserved E box elements in the large first intron. Additionally, we found that these elements are bound in vitro by CeTwist and its transcription factor partner, CeE/DA. The E box driven expression is eliminated or diminished in an hlh-8 null allele or in hlh-2 (CeE/DA) RNAi, respectively. Expression of hlh-8 is also diminished in animals harboring an hlh-8 intron deletion allele. Altogether, our results support a model in which hlh-8 is initially expressed in the undifferentiated M lineage cells via promoter elements and then the CeTwist activates its own expression further (autoregulation) in differentiated cells derived from the M lineage via the intron elements. This model provides a mechanism for how a transcription factor may regulate distinct target genes in cells both before and after initiating the differentiation program. The findings could also be relevant to understanding human Twist gene regulation, which is currently not well understood. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:224 / 236
页数:13
相关论文
共 29 条
[1]   SPLICING IN CAENORHABDITIS-ELEGANS DOES NOT REQUIRE AN AG AT THE 3' SPLICE ACCEPTOR SITE [J].
AROIAN, RV ;
LEVY, AD ;
KOGA, M ;
OHSHIMA, Y ;
KRAMER, JM ;
STERNBERG, PW .
MOLECULAR AND CELLULAR BIOLOGY, 1993, 13 (01) :626-637
[2]  
BRENNER S, 1974, GENETICS, V77, P71
[3]  
Corsi AK, 2000, DEVELOPMENT, V127, P2041
[4]  
Corsi AK, 2002, DEVELOPMENT, V129, P2761
[5]   The embryonic muscle transcriptome of Caenorhabditis elegans [J].
Fox, Rebecca M. ;
Watson, Joseph D. ;
Von Stetina, Stephen E. ;
McDermott, Joan ;
Brodigan, Thomas M. ;
Fukushige, Tetsunari ;
Krause, Michael ;
Miller, David M., III .
GENOME BIOLOGY, 2007, 8 (09)
[6]   The TWIST1 oncogene is a direct target of hypoxia-inducible factor-2α [J].
Gort, E. H. ;
van Haaften, G. ;
Verlaan, I. ;
Groot, A. J. ;
Plasterk, R. H. A. ;
Shvarts, A. ;
Suijkerbuijk, K. P. M. ;
van Laar, T. ;
van der Wall, E. ;
Raman, V. ;
van Diest, P. J. ;
Tijsterman, M. ;
Vooijs, M. .
ONCOGENE, 2008, 27 (11) :1501-1510
[7]   A Multiparameter Network Reveals Extensive Divergence between C. elegans bHLH Transcription Factors [J].
Grove, Christian A. ;
De Masi, Federico ;
Barrasa, M. Inmaculada ;
Newburger, Daniel E. ;
Alkema, Mark J. ;
Bulyk, Martha L. ;
Walhout, Albertha J. M. .
CELL, 2009, 138 (02) :314-327
[8]   Analysis of a Caenorhabditis elegans Twist homolog identifies conserved and divergent aspects of mesodermal patterning [J].
Harfe, BD ;
Gomes, AV ;
Kenyon, C ;
Liu, J ;
Krause, M ;
Fire, A .
GENES & DEVELOPMENT, 1998, 12 (16) :2623-2635
[9]  
Harfe BD, 1998, DEVELOPMENT, V125, P2479
[10]  
Harfe BD, 1998, DEVELOPMENT, V125, P421