Literature DB >> 9187147

The allocation of early blastomeres to the ectoderm and endoderm is variable in the sea urchin embryo.

C Y Logan1, D R McClay.   

Abstract

During sea urchin development, a tier-to-tier progression of cell signaling events is thought to segregate the early blastomeres to five different cell lineages by the 60-cell stage (E. H. Davidson, 1989, Development 105, 421-445). For example, the sixth equatorial cleavage produces two tiers of sister cells called 'veg1' and 'veg2,' which were projected by early studies to be allocated to the ectoderm and endoderm, respectively. Recent in vitro studies have proposed that the segregation of veg1 and veg2 cells to distinct fates involves signaling between the veg1 and veg2 tiers (O. Khaner and F. Wilt, 1991, Development 112, 881-890). However, fate-mapping studies on 60-cell stage embryos have not been performed with modern lineage tracers, and cell interactions between veg1 and veg2 cells have not been shown in vivo. Therefore, as an initial step towards examining how archenteron precursors are specified, a clonal analysis of veg1 and veg2 cells was performed using the lipophilic dye, DiI(C16), in the sea urchin species, Lytechinus variegatus. Both veg1 and veg2 descendants form archenteron tissues, revealing that the ectoderm and endoderm are not segregated at the sixth cleavage. Also, this division does not demarcate cell type boundaries within the endoderm, because both veg1 and veg2 descendants make an overlapping range of endodermal cell types. The allocation of veg1 cells to ectoderm and endoderm during cleavage is variable, as revealed by both the failure of veg1 descendants labeled at the eighth equatorial division to segregate predictably to either tissue and the large differences in the numbers of veg1 descendants that contribute to the ectoderm. Furthermore, DiI-labeled mesomeres of 32-cell stage embryos also contribute to the endoderm at a low frequency. These results show that the prospective archenteron is produced by a larger population of cleavage-stage blastomeres than believed previously. The segregation of veg1 cells to the ectoderm and endoderm occurs relatively late during development and is unpredictable, indicating that later cell position is more important than the early cleavage pattern in determining ectodermal and archenteron cell fates.

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Year:  1997        PMID: 9187147     DOI: 10.1242/dev.124.11.2213

Source DB:  PubMed          Journal:  Development        ISSN: 0950-1991            Impact factor:   6.868


  15 in total

1.  Molecular heterotopy in the expression of Brachyury orthologs in order Clypeasteroida (irregular sea urchins) and order Echinoida (regular sea urchins).

Authors:  Taku Hibino; Yoshito Harada; Takuya Minokawa; Masaru Nonaka; Shonan Amemiya
Journal:  Dev Genes Evol       Date:  2004-09-15       Impact factor: 0.900

2.  Clonal analyses reveal roles of organ founding stem cells, melanocyte stem cells and melanoblasts in establishment, growth and regeneration of the adult zebrafish fin.

Authors:  Shu Tu; Stephen L Johnson
Journal:  Development       Date:  2010-10-27       Impact factor: 6.868

3.  A gene regulatory network controlling the embryonic specification of endoderm.

Authors:  Isabelle S Peter; Eric H Davidson
Journal:  Nature       Date:  2011-05-29       Impact factor: 49.962

4.  Predictive computation of genomic logic processing functions in embryonic development.

Authors:  Isabelle S Peter; Emmanuel Faure; Eric H Davidson
Journal:  Proc Natl Acad Sci U S A       Date:  2012-08-27       Impact factor: 11.205

5.  Autonomy in specification of primordial germ cells and their passive translocation in the sea urchin.

Authors:  Mamiko Yajima; Gary M Wessel
Journal:  Development       Date:  2012-10       Impact factor: 6.868

Review 6.  Morphogenesis in sea urchin embryos: linking cellular events to gene regulatory network states.

Authors:  Deirdre C Lyons; Stacy L Kaltenbach; David R McClay
Journal:  Wiley Interdiscip Rev Dev Biol       Date:  2011-12-27       Impact factor: 5.814

7.  Encoding regulatory state boundaries in the pregastrular oral ectoderm of the sea urchin embryo.

Authors:  Enhu Li; Miao Cui; Isabelle S Peter; Eric H Davidson
Journal:  Proc Natl Acad Sci U S A       Date:  2014-02-20       Impact factor: 11.205

8.  ABCC5 is required for cAMP-mediated hindgut invagination in sea urchin embryos.

Authors:  Lauren E Shipp; Rose Z Hill; Gary W Moy; Tufan Gökırmak; Amro Hamdoun
Journal:  Development       Date:  2015-09-22       Impact factor: 6.868

9.  Hedgehog signaling patterns mesoderm in the sea urchin.

Authors:  Katherine D Walton; Jacob Warner; Philip H Hertzler; David R McClay
Journal:  Dev Biol       Date:  2009-04-23       Impact factor: 3.582

10.  The endoderm gene regulatory network in sea urchin embryos up to mid-blastula stage.

Authors:  Isabelle S Peter; Eric H Davidson
Journal:  Dev Biol       Date:  2009-11-03       Impact factor: 3.582

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