Lumen morphogenesis in C-elegans requires the membrane-cytoskeleton linker erm-1

被引:125
作者
Göbel, V
Barrett, PL
Hall, DH
Fleming, JT
机构
[1] Massachusetts Gen Hosp, Lab Dev Immunol, Boston, MA 02114 USA
[2] Harvard Univ, Sch Med, Dept Pediat, Boston, MA 02114 USA
[3] Yeshiva Univ Albert Einstein Coll Med, Dept Neurosci, Ctr C Elegans Anat, Bronx, NY 10461 USA
关键词
D O I
10.1016/j.devcel.2004.05.018
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Epithelial tubes are basic building blocks of complex organs, but their architectural requirements are not well understood. Here we show that erm-1 is a unique C. elegans ortholog of the ERM family of cytoskeleton-membrane linkers, with an essential role in lumen morphogenesis. ERM-1 localizes to the luminal membranes of those tubular organ epithelia which lack stabilization by cuticle. RNA interference (RNAi), a germline deletion, and overexpression of erm-1 cause cystic luminal phenotypes in these epithelia. Confocal and ultrastructural analyses indicate that erm-1 functions directly in apical membrane morphogenesis, rather than in epithelial polarity and junction assembly as has been previously proposed for ERMs. We also show that act-5/cytoplasmic actin and sma-1/ P-H-spectrin are required for lumen formation and functionally interact with erm-1. Our findings suggest that there are common structural constraints on the architecture of diverse organ lumina.
引用
收藏
页码:865 / 873
页数:9
相关论文
共 23 条
[1]   A C-elegans CLIC-like protein required for intracellular tube formation and maintenance [J].
Berry, KL ;
Bülow, HE ;
Hall, DH ;
Hobert, O .
SCIENCE, 2003, 302 (5653) :2134-2137
[2]   Zonula adherens formation in Caenorhabditis elegans requires dlg-1, the homologue of the Drosophila gene discs large [J].
Bossinger, O ;
Klebes, A ;
Segbert, C ;
Theres, C ;
Knust, E .
DEVELOPMENTAL BIOLOGY, 2001, 230 (01) :29-42
[3]   ERM proteins and merlin: Integrators at the cell cortex [J].
Bretscher, A ;
Edwards, K ;
Fehon, RG .
NATURE REVIEWS MOLECULAR CELL BIOLOGY, 2002, 3 (08) :586-599
[4]   Cystic canal mutants in Caenorhabditis elegans are defective in the apical membrane domain of the renal (excretory) cell [J].
Buechner, M ;
Hall, DH ;
Bhatt, H ;
Hedgecock, EM .
DEVELOPMENTAL BIOLOGY, 1999, 214 (01) :227-241
[5]   A putative catenin-cadherin system mediates morphogenesis of the Caenorhabditis elegans embryo [J].
Costa, M ;
Raich, W ;
Agbunag, C ;
Leung, B ;
Hardin, J ;
Priess, JR .
JOURNAL OF CELL BIOLOGY, 1998, 141 (01) :297-308
[6]   Potent and specific genetic interference by double-stranded RNA in Caenorhabditis elegans [J].
Fire, A ;
Xu, SQ ;
Montgomery, MK ;
Kostas, SA ;
Driver, SE ;
Mello, CC .
NATURE, 1998, 391 (6669) :806-811
[7]   PCR fusion-based approach to create reporter gene constructs for expression analysis in transgenic C-elegans [J].
Hobert, O .
BIOTECHNIQUES, 2002, 32 (04) :728-730
[8]   ASSEMBLY OF BODY-WALL MUSCLE AND MUSCLE-CELL ATTACHMENT STRUCTURES IN CAENORHABDITIS-ELEGANS [J].
HRESKO, MC ;
WILLIAMS, BD ;
WATERSTON, RH .
JOURNAL OF CELL BIOLOGY, 1994, 124 (04) :491-506
[9]   Epithelial tube morphogenesis during Drosophila tracheal development requires Piopio, a luminal ZP protein [J].
Jazwinska, A ;
Ribeiro, C ;
Affolter, M .
NATURE CELL BIOLOGY, 2003, 5 (10) :895-901
[10]   Effectiveness of specific RNA-mediated interference through ingested double-stranded RNA in Caenorhabditis elegans [J].
Kamath, Ravi S. ;
Martinez-Campos, Maruxa ;
Zipperlen, Peder ;
Fraser, Andrew G. ;
Ahringer, Julie .
GENOME BIOLOGY, 2001, 2 (01)