Literature DB >> 22006441

The echinoid mitotic gradient: effect of cell size on the micromere cleavage cycle.

Rosalie E Langelan Duncan1, Arthur H Whiteley.   

Abstract

Like other euechinoids, the fertilized eggs of the sand dollar Dendraster excentricus proceed through cleavages that produce a pattern of macromeres, mesomeres, and micromeres at the 4th division. The 8 cells of the macro-mesomere lineage proceed through 6 additional cleavages before hatching. At the fifth overall division, the 4 micromeres produce a lineage of large micromeres that will divide 3 additional times, and a lineage of small micromeres that will divide once more before hatching. Irrespective of lineage, the length of the cell cycles is closely related to the size of the blastomere; cells of the same size have the same cell cycle time. A consequence is that at the fourth cleavage, there is a gradient of mitotic activity from the fastest dividers at the animal pole and the slowest cleaving micromeres at the vegetal pole. By the time of hatching, which is the 10th division of meso-macromeres, all cells are the same small size, the metachronic pattern of division gives way to asynchrony, and the mitotic gradient along the polar axis is lost. Experimental pre-exposure to sodium dodecyl sulfate (SDS), however, blocks the appearance of the gradients in cell size, the mitotic gradient, and the differential in cell cycle times. It is proposed that the mitotic gradients, cell cycle times, and attainment of a state of asynchrony are functions of cell size. Developmental consequences of the transition are large, and include coordinated activation of transcriptions, synthesis of new patterns of proteins, alterations of metabolism, and onset of morphogenesis.
Copyright © 2011 Wiley Periodicals, Inc.

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Year:  2011        PMID: 22006441      PMCID: PMC3511907          DOI: 10.1002/mrd.21373

Source DB:  PubMed          Journal:  Mol Reprod Dev        ISSN: 1040-452X            Impact factor:   2.609


  18 in total

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Authors:  D P Easton; A H Whiteley
Journal:  Differentiation       Date:  1979       Impact factor: 3.880

2.  Histones and histone synthesis in sea urchin development.

Authors:  J V Ruderman; P R Gross
Journal:  Dev Biol       Date:  1974-02       Impact factor: 3.582

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Authors:  M A Harkey; A H Whiteley
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4.  A major developmental transition in early Xenopus embryos: I. characterization and timing of cellular changes at the midblastula stage.

Authors:  J Newport; M Kirschner
Journal:  Cell       Date:  1982-10       Impact factor: 41.582

5.  Patterns of protein synthesis and metabolism during sea urchin embryogenesis.

Authors:  P A Bédard; B P Brandhorst
Journal:  Dev Biol       Date:  1983-03       Impact factor: 3.582

6.  Developmental time, cell lineage, and environment regulate the newly synthesized proteins in sea urchin embryos.

Authors:  D Pittman; S G Ernst
Journal:  Dev Biol       Date:  1984-11       Impact factor: 3.582

7.  Studies on dwarf larvae developed from isolated blastomeres of the starfish. Asterina pectinifera.

Authors:  M Dan-Sohkawa; N Satoh
Journal:  J Embryol Exp Morphol       Date:  1978-08

8.  A major developmental transition in early Xenopus embryos: II. Control of the onset of transcription.

Authors:  J Newport; M Kirschner
Journal:  Cell       Date:  1982-10       Impact factor: 41.582

9.  Nanos functions to maintain the fate of the small micromere lineage in the sea urchin embryo.

Authors:  Celina E Juliano; Mamiko Yajima; Gary M Wessel
Journal:  Dev Biol       Date:  2009-10-28       Impact factor: 3.582

10.  Unequal cleavage and the differentiation of echinoid primary mesenchyme.

Authors:  R E Langelan; A H Whiteley
Journal:  Dev Biol       Date:  1985-06       Impact factor: 3.582

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  2 in total

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  2 in total

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