Lineage and fate of each blastomere of the eight-cell sea urchin embryo
Abstract
A fluoresceinated lineage tracer was injected into individual blastomeres of eight-cell sea urchin (Strongylocentrotus purpuratus) embryos, and the location of the progeny of each blastomere was determined in the fully developed pluteus. Each blastomere gives rise to a unique portion of the advanced embryo. We confirm many of the classical assignments of cell fate along the animal-vegetal axis of the cleavage-stage embryo, and demonstrate that one blastomere of the animal quartet at the eight-cell stage lies nearest the future oral pole and the opposite one nearest the future aboral pole of the embryo. Clones of cells deriving from ectodermal founder cells always remain contiguous, while clones of cells descendant from the vegetal plate (i.e., gut, secondary mesenchyme) do not. The locations of ectodermal clones contributed by specific blastomeres require that the larval plane of bilateral symmetry lie approximately equidistant (i.e., at a 45 degree angle) from each of the first two cleavage planes. These results underscore the conclusion that many of the early spatial patterns of differential gene expression observed at the molecular level are specified in a clonal manner early in embryonic sea urchin development, and are each confined to cell lineages established during cleavage.
Additional Information
© 1987 by Cold Spring Harbor Laboratory. Received December 8, 1986; accepted December 24, 1986. We thank Ronald Hill for technical assistance. Robert L. Gimlich kindly provided fluoresceinated dextran. This work was supported by National Science Foundation grant DCB 8544707 to R.A.C., by National Institutes of Health Grant HD-05753 to E.H.D., and by National Institutes of Health Biomedical Research Support grant RR07003.Attached Files
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Additional details
- Eprint ID
- 35020
- Resolver ID
- CaltechAUTHORS:20121023-083116845
- NSF
- DCB-8544707
- NIH
- HD-05753
- NIH
- RR07003
- Created
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2012-10-23Created from EPrint's datestamp field
- Updated
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2021-11-09Created from EPrint's last_modified field