Expression and function of members of a divergent nuclear receptor family in Caenorhabditis elegans

被引:106
作者
Miyabayashi, T
Palfreyman, MT
Sluder, AE
Slack, F
Sengupta, P [1 ]
机构
[1] Brandeis Univ, Dept Biol, Waltham, MA 02454 USA
[2] Brandeis Univ, Volen Ctr Complex Syst, Waltham, MA 02454 USA
[3] Asahi Chem Ind Co Ltd, Fuji, Shizuoka 416, Japan
[4] Univ Georgia, Dept Cellular Biol, Athens, GA 30602 USA
[5] Harvard Univ, Sch Med, Dept Genet, Boston, MA 02114 USA
[6] Massachusetts Gen Hosp, Dept Mol Biol, Boston, MA 02114 USA
基金
美国国家卫生研究院;
关键词
nuclear receptors; C-elegans; expression pattern; overexpression; hypodermal seam cells;
D O I
10.1006/dbio.1999.9470
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Nuclear receptors (NRs) are a large class of ligand-regulated transcriptional modulators that have been shown to play roles in many developmental processes. The Caenorhabditis elegans genome is predicted to encode a large and divergent family of NR proteins. The functions of most of these genes are unknown. As a first step toward defining their roles, we have initiated an expression and functional survey of a subset of these genes. In this study, we demonstrate expression of 21 of 28 NR genes examined, indicating that a large fraction of the predicted genes likely encode functional gene products. We show that five genes are expressed predominantly in neuronal cells, while others are expressed in multiple cell types. Interestingly, we find that eight genes are expressed exclusively in the lateral hypodermal (seam) cells. These eight genes share a high degree of overall homology and cluster in a neighbor-joining tree derived from sequence analysis of the NRs, suggesting that they arose by gene duplication from a common ancestor. We show that overexpression of each of three members of this subfamily results in similar developmental defects, consistent with a redundant role for these genes in the function of the lateral hypodermal cells. (C) 1999 Academic Press.
引用
收藏
页码:314 / 331
页数:18
相关论文
共 97 条
[1]   BASIC LOCAL ALIGNMENT SEARCH TOOL [J].
ALTSCHUL, SF ;
GISH, W ;
MILLER, W ;
MYERS, EW ;
LIPMAN, DJ .
JOURNAL OF MOLECULAR BIOLOGY, 1990, 215 (03) :403-410
[2]  
Antebi A, 1998, DEVELOPMENT, V125, P1191
[3]   BXR, an embryonic orphan nuclear receptor activated by a novel class of endogenous benzoate metabolites [J].
Blumberg, B ;
Kang, HJ ;
Bolado, J ;
Chen, HW ;
Craig, AG ;
Moreno, TA ;
Umesono, K ;
Perlmann, T ;
De Robertis, EM ;
Evans, RM .
GENES & DEVELOPMENT, 1998, 12 (09) :1269-1277
[4]   Orphan nuclear receptors - new ligands and new possibilities [J].
Blumberg, B ;
Evans, RM .
GENES & DEVELOPMENT, 1998, 12 (20) :3149-3155
[5]  
BRENNER S, 1974, GENETICS, V77, P71
[6]   Mutations in a C-elegans G(q)alpha gene disrupt movement, egg laying, and viability [J].
Brundage, L ;
Avery, L ;
Katz, A ;
Kim, UJ ;
Mendel, JE ;
Sternberg, PW ;
Simon, MI .
NEURON, 1996, 16 (05) :999-1009
[7]   The nuclear hormone receptor SEX-1 is an X-chromosome signal that determines nematode sex [J].
Carmi, I ;
Kopczynski, JB ;
Meyer, BJ .
NATURE, 1998, 396 (6707) :168-173
[8]   Role of CBP/P300 in nuclear receptor signalling [J].
Chakravarti, D ;
LaMorte, VJ ;
Nelson, MC ;
Nakajima, T ;
Schulman, IG ;
Juguilon, H ;
Montminy, M ;
Evans, RM .
NATURE, 1996, 383 (6595) :99-103
[9]   GREEN FLUORESCENT PROTEIN AS A MARKER FOR GENE-EXPRESSION [J].
CHALFIE, M ;
TU, Y ;
EUSKIRCHEN, G ;
WARD, WW ;
PRASHER, DC .
SCIENCE, 1994, 263 (5148) :802-805
[10]  
CHEN LS, 1994, DEVELOPMENT, V120, P1631