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[
WormBook,
2005]
Basement membranes are thin, specialized extracellular matrices surrounding most tissues in all metazoans. The compositions and functions of basement membranes have generally been well conserved throughout the subkingdom. Genetic analyses of basement membrane components in C. elegans have provided insights into their assembly and functions during development. Immuno- or GFP-tagged localization studies have shown that basement membranes on different tissues, or even sub-regions of tissues, contain different sets of proteins or alternatively spliced isoforms of them. Several components, including laminin, perlecan, type IV collagen and possibly osteonectin/SPARC, are essential for completion of embryogenesis, being necessary for tissue organization and structural integrity. In contrast, type XVIII collagen and nidogen are not required for viability but primarily influence organization of the nervous system. All of these proteins, with the exception of nidogen and the addition of fibulin, have roles of varying degree in morphogenesis of the gonad. A major family of cellular receptors for basement membrane proteins, the integrins, have also been characterized in C. elegans. As one might expect, integrins have been shown to function in many of the same processes as their potential ligands, the basement membrane components. While much remains to be explored, studies of basement membranes in C. elegans have been highly informative and hold great promise for improving our understanding of how these structures are assembled and how they function in development.
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[
FASEB J,
1994]
Two types of collagens have been identified in Caenorhabditis elegans corresponding to two types of extracellular matrix, the cuticle and basement membranes. Cuticle collagens are encoded by a developmentally regulated family of similar to 100 genes. Mutations in cuticle collagens can produce animals that are longer or shorter than normal and/or that are helically twisted. Mutations in different collagens can cause different morphological abnormalities, as can different mutations in the same collagen. Genetic interactions between collagen genes have been described and may identify collagens that interact to form the cuticle. Two basement membrane (type IV) collagen genes have been identified in C. elegans. They encode proteins similar in structure to vertebrate type IV collagen. One of the genes produces two alternatively spliced forms, one predominantly expressed in embryos and the other in larvae and adults, suggesting that embryonic basement membranes may have unique properties. Most mutations in the type IV genes cause embryonic lethality, indicating that normal basement membranes are required for embryogenesis. Temperature-sensitive mutations have been used to show that type IV collagen function is also required for larval development and adult fertility.
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[
Annu Rev Genet,
1994]
All metazoans possess extracellular matrices (ECM) composed of complex assemblies of molecules with generally well conserved structures and functions. ECM play structural roles, providing scaffolds that organize and strengthen tissues, and instructional roles, influencing differentiation and development. Major ECM components include the collagens, a diverse family of fibrous proteins distinguished by their triple-helical coiled coil structure, other large glycoproteins, such as laminin, fibronectin and nidogen, and proteoglycans, proteins with attached glycosaminoglycan chains. For most ECM components, cell surface receptors have been identified that can mediate interactions between the cell and its ECM. The nematode Caenorhabditis elegans is an excellent system for studies of the structures and functions of ECM components, and their roles in development. C. elegans is the simplest metazoan in which detailed genetic analysis of the ECM can be performed. The complete cell lineage and detailed anatomical structure of the organism have been described. The simple life style of C. elegans allows animals with severe morphological and/or motility defects to survive and, because they are internally self-fertilizing hermaphrodites, even reproduce. These properties can simplify mutational analyses of genes encoding ECM components. Two major forms of ECM have been identified in C. elegans, the cuticle and basement membranes. The cuticle, or exoskeleton, covers the outside of the animal and lines the lumen of the pharynx. Basement membranes cover the pseudocoelomic faces of the pharynx, intestine, gonad, and hypodermis. There is no visible interstitial matrix between the cells within tissues, possibly because nearly all cells are adjacent to the cuticle or a basement membrane. This review focuses on studies of the ECM in C. elegans. The reader is referred to excellent recent reviews concerning related topics: collagens in other nematodes; mutations in human fibrillar collagens; mutations in human type IV collagen; composition
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[
Sci STKE,
2000]
Notch proteins are receptors that are important in mediating several developmental processes. Notch receptors are activated upon binding transmembrane ligands, the DSL proteins. Notch is cleaved at several sites and activation of Notch leads to the cleavage of the intracellular domain, which then is translocated to the nucleus and regulates the transcription of target genes. Kramer discusses how binding of Notch to the DSL ligand, Delta, leads to cleavage and trans-endocytosis of the Notch extracellular domain into the Delta-expressing cell. This trans-endocytosis event contributes to the cleavage and release of the active Notch intracellular domain. The Perspective is accompanied by a movie illustrating the trans-endocytosis of Notch.
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[
International Journal of Developmental Biology,
1998]
Pleiotropy , a situation in which a single gene influences multiple phenotypic tra its, can arise in a variety of ways. This paper discusses possible underlying mechanisms and proposes a classification of the various phenomena involved.
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[
Curr Biol,
2003]
A novel protein in Caenorhabditis elegans, SAS-4, is a component of centrioles and is required for centriole duplication. Depletion of SAS-4 results in stunted centrioles and a smaller centrosome, suggesting a link to organelle size control.
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[
Curr Biol,
1997]
An increasing body of evidence indicates that
p53, the product of a tumour suppressor gene, has a role in development - could this developmental role have provided the primary driving force in the evolution of a protein best known as a stress-response integrator?
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[
Genome Biol,
2009]
Comparison of a regulatory network that specifies dopaminergic neurons in Caenorhabditis elegans to the development of vertebrate dopamine systems in the mouse reveals a possible partial conservation of such a network.
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[
Nature,
1990]
What molecular signalling machines tell a precursor cell to develop into a specialized structure? In one case, described in three papers, including that by Aroian et al. on page 693 of this issue, these machines turn out to be a receptor tyrosine kinase and a ras protein.
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[
Curr Biol,
2000]
A second case has been found of a nematode gene involved in developmental timing that encodes a short, non-coding RNA. Both RNAs are expressed at specific times and appear to repress target genes by interacting with their 3' untranslated regions. A coincidence? Or does this pathway attract small RNA regulators?