The role of the ELAV homologue EXC-7 in the development of the Caenorhabditis elegans excretory canals

被引:29
作者
Fujita, M
Hawkinson, D
King, KV
Hall, DH
Sakamoto, H
Buechner, M
机构
[1] Univ Kansas, Dept Mol Biosci, Lawrence, KS 66045 USA
[2] Kobe Univ, Grad Sch Sci & Technol, Dept Biol, Nada Ku, Kobe, Hyogo 6578501, Japan
[3] Albert Einstein Coll Med, Ctr C Elegans Anat, Dept Neurosci, Bronx, NY 10461 USA
关键词
ELAV; RNA-binding; epithelial polarity; spectrin; excretory canals; apical cytoskeleton;
D O I
10.1016/S0012-1606(03)00040-X
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
The exc mutations of Caenorhabditis elegans alter the position and shape of the apical cytoskeleton in polarized epithelial cells. Mutants in exc-7 form small cysts throughout the tubular excretory canals that regulate organismal osmolarity. We have cloned the exc-7 gene, the closest nematode homologue to the neural RNA-binding protein ELAV. EXC-7 is expressed in the canal for a short time midway through embryogenesis. Cysts in exc-7 mutants do not develop until several hours later, beginning at the time of hatching. We find that the first larval period is when the canal completes the majority of its outgrowth, and adds new apical cytoskeleton at a rapid rate. Ultrastructural studies show that exc-7 mutant defects resemble loss of beta(H)-spectrin (encoded by sma-1) at the distal ends of the excretory canals. In addition, exc-7 mutants exhibit synergistic excretory canal defects with mutations in sma-1, and EXC-7 binds sma-1 mRNA. These data imply that EXC-7 protein may affect expression of sma-1 and other genes to effect proper development of the excretory canals. (C) 2003 Elsevier Science (USA). All rights reserved.
引用
收藏
页码:290 / 301
页数:12
相关论文
共 60 条
[11]   Genome sequence of the nematode C-elegans:: A platform for investigating biology [J].
不详 .
SCIENCE, 1998, 282 (5396) :2012-2018
[12]   MUTANT ALLELES AT THE LOCUS ELAV IN DROSOPHILA-MELANOGASTER LEAD TO NERVOUS-SYSTEM DEFECTS - A DEVELOPMENTAL GENETIC-ANALYSIS [J].
CAMPOS, AR ;
GROSSMAN, D ;
WHITE, K .
JOURNAL OF NEUROGENETICS, 1985, 2 (03) :197-218
[13]   Binding of a 40-kDa protein to the N-myc 3'-untranslated region correlates with enhanced N-myc expression in human neuroblastoma [J].
Chagnovich, D ;
Cohn, SL .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1996, 271 (52) :33580-33586
[14]  
Chitwood M. B., 1974, INTRO NEMATOLOGY, P126
[15]   RNA interference is mediated by 21-and 22-nucleotide RNAs [J].
Elbashir, SM ;
Lendeckel, W ;
Tuschl, T .
GENES & DEVELOPMENT, 2001, 15 (02) :188-200
[16]   Overexpression of HuR, a nuclear-cytoplasmic shuttling protein, increases the in vivo stability of ARE-containing mRNAs [J].
Fan, XHC ;
Steitz, JA .
EMBO JOURNAL, 1998, 17 (12) :3448-3460
[17]   ELAV proteins stabilize deadenylated intermediates in a novel in vitro mRNA deadenylation/degradation system [J].
Ford, LP ;
Watson, J ;
Keene, JD ;
Wilusz, J .
GENES & DEVELOPMENT, 1999, 13 (02) :188-201
[18]   Neuronal expression of a Caenorhabditis elegans elav-like gene and the effect of its ectopic expression [J].
Fujita, M ;
Kawano, T ;
Ohta, A ;
Sakamoto, H .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1999, 260 (03) :646-652
[19]   Protein ligands mediate the CRM1-dependent export of HuR in response to heat shock [J].
Gallouzi, IE ;
Brennan, CM ;
Steitz, JA .
RNA, 2001, 7 (09) :1348-1361
[20]   Delineation of mRNA export pathways by the use of cell-permeable peptides [J].
Gallouzi, IE ;
Steitz, JA .
SCIENCE, 2001, 294 (5548) :1895-1901