The hedgehog-related gene qua-1 is required for molting in Caenorhabditis elegans

被引:38
作者
Hao, Limin
Mukherjee, Krishanu
Liegeois, Samuel
Baillie, David
Labouesse, Michel
Burglin, Thomas R. [1 ]
机构
[1] Karolinska Inst, Dept Biosci & Nutr, Huddinge, Sweden
[2] Karolinska Inst, Ctr Genom & Bioinformat, Huddinge, Sweden
[3] Sodertorns Hogskola, Sch Life Sci, Huddinge, Sweden
[4] ULP, INSERM, CNRS, Inst Genet & Biol Mol & Cellulaire,CU Strasbourg, Illkirch Graffenstaden, France
[5] Simon Fraser Univ, Dept Mol Biol & Biochem, Burnaby, BC V5A 1S6, Canada
关键词
Caenorhabditis elegans; hedgehog; hint; molting; cuticle; qua-1;
D O I
10.1002/dvdy.20721
中图分类号
R602 [外科病理学、解剖学]; R32 [人体形态学];
学科分类号
100101 ;
摘要
The Caenorhabditis elegans genome encodes ten proteins that share similarity with Hedgehog through the C-terminal Hint/Hog domain. While most genes are members of larger gene families, qua-1 is a single copy gene. Here we show that orthologs of qua-1 exist in many nematodes, including Brugia malayi, which shared a common ancestor with C. elegans about 300 million years ago. The QUA-1 proteins contain an N-terminal domain, the Qua domain, that is highly conserved, but whose molecular function is not known. We have studied the expression pattern of qua-1 in C. elegans using a qua-1::GFP transcriptional fusion. qua-1 is mainly expressed in hyp1 to hyp11 hypodermal cells, but not in seam cells. It is also expressed in intestinal and rectal cells, sensilla support cells, and the P cell lineage in L1. The expression of qua-1::GFP undergoes cyclical changes during development in phase with the molting cycle. It accumulates prior to molting and disappears between molts. Disruption of the qua-1 gene function through an internal deletion that causes a frame shift with premature stop in the middle of the gene results in strong lethality. The animals arrest in the early larval stages due to defects in molting. Electron microscopy reveals double cuticles due to defective ecdysis, but no obvious defects are seen in the hypodermis. Qua domain-only::GFP and full-length QUA-1::GFP fusion constructs are secreted and associated with the overlying cuticle, but only QUA-1::GFP rescues the mutant phenotype. Our results suggest that both the Hint/Hog domain and Qua domain are critically required for the function of QUA-1.
引用
收藏
页码:1469 / 1481
页数:13
相关论文
共 47 条
[1]   Evidence for a clade of nematodes, arthropods and other moulting animals [J].
Aguinaldo, AMA ;
Turbeville, JM ;
Linford, LS ;
Rivera, MC ;
Garey, JR ;
Raff, RA ;
Lake, JA .
NATURE, 1997, 387 (6632) :489-493
[2]   Gapped BLAST and PSI-BLAST: a new generation of protein database search programs [J].
Altschul, SF ;
Madden, TL ;
Schaffer, AA ;
Zhang, JH ;
Zhang, Z ;
Miller, W ;
Lipman, DJ .
NUCLEIC ACIDS RESEARCH, 1997, 25 (17) :3389-3402
[3]   The conserved nuclear receptor Ftz-F1 is required for embryogenesis, moulting and reproduction in Caenorhabditis elegans [J].
Asahina, M ;
Ishihara, T ;
Jindra, M ;
Kohara, Y ;
Katsura, I ;
Hirose, S .
GENES TO CELLS, 2000, 5 (09) :711-723
[4]   Caenorhabditis elegans has scores of hedgehog-related genes:: Sequence and expression analysis [J].
Aspöck, G ;
Kagoshima, H ;
Niklaus, G ;
Bürglin, TR .
GENOME RESEARCH, 1999, 9 (10) :909-923
[5]  
Beachy PA, 1997, COLD SPRING HARB SYM, V62, P191
[6]   Improved prediction of signal peptides: SignalP 3.0 [J].
Bendtsen, JD ;
Nielsen, H ;
von Heijne, G ;
Brunak, S .
JOURNAL OF MOLECULAR BIOLOGY, 2004, 340 (04) :783-795
[7]   mua-3, a gene required for mechanical tissue integrity in Caenorhabditis elegans, encodes a novel transmembrane protein of epithelial attachment complexes [J].
Bercher, M ;
Wahl, J ;
Vogel, BE ;
Lu, C ;
Hedgecock, EM ;
Hall, DH ;
Plenefisch, JD .
JOURNAL OF CELL BIOLOGY, 2001, 154 (02) :415-426
[8]   A molecular evolutionary framework for the phylum Nematoda [J].
Blaxter, ML ;
De Ley, P ;
Garey, JR ;
Liu, LX ;
Scheldeman, P ;
Vierstraete, A ;
Vanfleteren, JR ;
Mackey, LY ;
Dorris, M ;
Frisse, LM ;
Vida, JT ;
Thomas, WK .
NATURE, 1998, 392 (6671) :71-75
[9]   An essential role in molting and morphogenesis of Caenorhabditis elegans for ACN-1, a novel member of the angiotensin-converting enzyme family that lacks a metallopeptidase active site [J].
Brooks, DR ;
Appleford, PJ ;
Murray, L ;
Isaac, RE .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (52) :52340-52346
[10]  
Burglin T R., 1994, Guidebook to the homeobox genes, P27, DOI [10.1093/oso/9780198599395.003.0003, DOI 10.1093/OSO/9780198599395.003.0003]