Abstract:Embryogenesis of the free-living soil nematodeCaenorhabditis elegans produces a juvenile having about 550 cells at hatching. We have determined the lineages of 182 cells by tracing the divisions of individual cells in living embryos. An invariant pattern of cleavage divisions of the egg generates a set of stem cells. These stem cells are the founders of six stem cell lineages. Each lineage has its own clock-i.e., an autonomous rhythm of synchronous cell divisions. The rhythms are maintained in spite of extensi… Show more
“…The intestine is not only responsible for assimilation and digestion of food but also for synthesis and storage of macromolecules such as yolk proteins [McGhee, 2007]. A single cell, the E-blastomere of the eight-cell embryo, gives rise to the entire intestine [Deppe et al, 1978;Sulston et al, 1983;Leung et al, 1999]. The E-cell divides in a stereotypic pattern leading to a defined arrangement of the resulting 20 cells which encircle the intestinal lumen as a series of nine rings referred to as ''ints'' [ Fig.…”
Section: Intermediate Filaments In the C Elegans Intestinementioning
Intermediate filaments (IFs) make up one of the three major fibrous cytoskeletal systems in metazoans. Numerous IF polypeptides are synthesized in cell typespecific combinations suggesting specialized functions. The review concentrates on IFs in the model organism Caenorhabditis elegans which carries great promise to elucidate the still unresolved mechanisms of IF assembly into complex networks and to determine IF function in a living organism. In contrast to Drosophila melanogaster, which lacks cytoplasmic IFs altogether, the nematode genome contains 11 genes coding for cytoplasmic IFs and only a single gene for a nuclear lamin. Its cytoplasmic IFs are expressed in developmentally and spatially defined patterns. As an example we present the case of the intestinal IFs which are abundant in the mechanically resilient endotube, a prominent feature of the C. elegans intestinal terminal web region. This IF-rich structure brings together all three cytoskeletal filaments that are integrated into a coherent entity by the C. elegans apical junction (CeAJ) thereby completely surrounding and stabilizing the intestinal lumen with its characteristic brush border. Concepts on the developmental establishment of the endotube in relation to polarization and its function for maintenance of epithelial integrity are discussed. Furthermore, possible connections of the cytoplasmic cytoskeleton to the nuclear lamin IFs and the importance of these links for nuclear positioning are summarized. Cell
“…The intestine is not only responsible for assimilation and digestion of food but also for synthesis and storage of macromolecules such as yolk proteins [McGhee, 2007]. A single cell, the E-blastomere of the eight-cell embryo, gives rise to the entire intestine [Deppe et al, 1978;Sulston et al, 1983;Leung et al, 1999]. The E-cell divides in a stereotypic pattern leading to a defined arrangement of the resulting 20 cells which encircle the intestinal lumen as a series of nine rings referred to as ''ints'' [ Fig.…”
Section: Intermediate Filaments In the C Elegans Intestinementioning
Intermediate filaments (IFs) make up one of the three major fibrous cytoskeletal systems in metazoans. Numerous IF polypeptides are synthesized in cell typespecific combinations suggesting specialized functions. The review concentrates on IFs in the model organism Caenorhabditis elegans which carries great promise to elucidate the still unresolved mechanisms of IF assembly into complex networks and to determine IF function in a living organism. In contrast to Drosophila melanogaster, which lacks cytoplasmic IFs altogether, the nematode genome contains 11 genes coding for cytoplasmic IFs and only a single gene for a nuclear lamin. Its cytoplasmic IFs are expressed in developmentally and spatially defined patterns. As an example we present the case of the intestinal IFs which are abundant in the mechanically resilient endotube, a prominent feature of the C. elegans intestinal terminal web region. This IF-rich structure brings together all three cytoskeletal filaments that are integrated into a coherent entity by the C. elegans apical junction (CeAJ) thereby completely surrounding and stabilizing the intestinal lumen with its characteristic brush border. Concepts on the developmental establishment of the endotube in relation to polarization and its function for maintenance of epithelial integrity are discussed. Furthermore, possible connections of the cytoplasmic cytoskeleton to the nuclear lamin IFs and the importance of these links for nuclear positioning are summarized. Cell
“…Caenorhabditis elegans was the first to benefit from comprehensive time-lapse imaging at a spatiotemporal resolution sufficient to trace all cells and cell divisions during development, using non-fluorescent differential interference contrast optics [4,5]. This allows an alternative approach for determining the lineage of cells -retrospective lineage analysis.…”
“…1; Deppe et al 1978;Sulston et al 1983). Each of the founder cells shows distinct rates of cell division and produces a unique repertoire of differentiated cell types.…”
The endoderm in the nematode Caenorhabditis elegans is clonally derived from the E founder cell. We identified a single genomic region (the endoderm-determining region, or EDR) that is required for the production of the entire C. elegans endoderm. In embryos lacking the EDR, the E cell gives rise to ectoderm and mesoderm instead of endoderm and appears to adopt the fate of its cousin, the C founder cell. end-1, a gene from the EDR, restores endoderm production in EDR deficiency homozygotes. end-1 transcripts are first detectable specifically in the E cell, consistent with a direct role for end-1 in endoderm development. The END-1 protein is an apparent zinc finger-containing GATA transcription factor. As GATA factors have been implicated in endoderm development in other animals, our findings suggest that endoderm may be specified by molecularly conserved mechanisms in triploblastic animals. We propose that end-1, the first zygotic gene known to be involved in the specification of germ layer and founder cell identity in C. elegans, may link maternal genes that regulate the establishment of the endoderm to downstream genes responsible for endoderm differentiation.
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