| pubmed-article:9133433 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:9133433 | lifeskim:mentions | umls-concept:C0205147 | lld:lifeskim |
| pubmed-article:9133433 | lifeskim:mentions | umls-concept:C0013936 | lld:lifeskim |
| pubmed-article:9133433 | lifeskim:mentions | umls-concept:C0205307 | lld:lifeskim |
| pubmed-article:9133433 | lifeskim:mentions | umls-concept:C1527148 | lld:lifeskim |
| pubmed-article:9133433 | lifeskim:mentions | umls-concept:C0162610 | lld:lifeskim |
| pubmed-article:9133433 | lifeskim:mentions | umls-concept:C0181839 | lld:lifeskim |
| pubmed-article:9133433 | lifeskim:mentions | umls-concept:C2827666 | lld:lifeskim |
| pubmed-article:9133433 | lifeskim:mentions | umls-concept:C2348235 | lld:lifeskim |
| pubmed-article:9133433 | pubmed:issue | 2 | lld:pubmed |
| pubmed-article:9133433 | pubmed:dateCreated | 1997-6-2 | lld:pubmed |
| pubmed-article:9133433 | pubmed:abstractText | Caenorhabditis elegans is renowned for its invariant embryogenesis. This pattern of development is in apparent contrast to other organisms from Drosophila to higher vertebrates. With the aid of a 4D microscope system (multifocal, time-lapse video recording system) which permits the extensive documentation and analysis of cell divisions, cell positions, and migrations in single embryos we have analyzed normal embryogenesis of C. elegans. The instrumentation reveals a naturally occurring variability in cell division timing, cell positioning, and cell-cell contacts which could not have been detected by the direct observation used earlier (Sulston et al., 1983, Dev. Biol. 100, 64-119). Embryos are very flexible and produce an essentially invariant premorphogenetic stage from variable earlier stages. An analysis of the distribution of the descendants of the early founder blastomeres at the premorphogenetic stage shows that these establish discrete regions in the embryo, a process involving a considerable amount of cell movement, which again varies in different embryos. Only cell fate assignment remains invariant. However, as shown earlier, this is not due to an autonomous invariant specification of cell fates but due to the fact that cell-cell interactions occur very early when the topology of blastomeres in the embryo is still sufficiently precise to ensure reproducible patterns of inductions. A new concept that founder blastomeres produce embryonic regions in the embryo can explain the striking complexity of the lineage per se and also the complicated asymmetric lineage patterns by which the bilateral symmetry of the embryo is established. Many cells, including bilateral homologs, were apparently chosen for a specific fate solely by their position in the embryo, irrespectively of the lineage descent by which the cells are created. We postulate that the production of regions by cell-cell interactions is the pivotal principle guiding the embryogenesis of C. elegans and that the embryogenesis of the worm follows the same basic principles as embryogenesis in other organisms. | lld:pubmed |
| pubmed-article:9133433 | pubmed:language | eng | lld:pubmed |
| pubmed-article:9133433 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9133433 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:9133433 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:9133433 | pubmed:month | Apr | lld:pubmed |
| pubmed-article:9133433 | pubmed:issn | 0012-1606 | lld:pubmed |
| pubmed-article:9133433 | pubmed:author | pubmed-author:SchnabelRR | lld:pubmed |
| pubmed-article:9133433 | pubmed:author | pubmed-author:SchnabelHH | lld:pubmed |
| pubmed-article:9133433 | pubmed:author | pubmed-author:HutterHH | lld:pubmed |
| pubmed-article:9133433 | pubmed:author | pubmed-author:MoermanDD | lld:pubmed |
| pubmed-article:9133433 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:9133433 | pubmed:day | 15 | lld:pubmed |
| pubmed-article:9133433 | pubmed:volume | 184 | lld:pubmed |
| pubmed-article:9133433 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:9133433 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:9133433 | pubmed:pagination | 234-65 | lld:pubmed |
| pubmed-article:9133433 | pubmed:dateRevised | 2006-11-15 | lld:pubmed |
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| pubmed-article:9133433 | pubmed:year | 1997 | lld:pubmed |
| pubmed-article:9133433 | pubmed:articleTitle | Assessing normal embryogenesis in Caenorhabditis elegans using a 4D microscope: variability of development and regional specification. | lld:pubmed |
| pubmed-article:9133433 | pubmed:affiliation | MPI für Biochemie, Martinsried, Germany. | lld:pubmed |
| pubmed-article:9133433 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:9133433 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
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