Literature DB >> 27402572

The diversity of nanos expression in echinoderm embryos supports different mechanisms in germ cell specification.

Tara Fresques1, Steven Zachary Swartz1, Celina Juliano1,2, Yoshiaki Morino3, Mani Kikuchi4, Koji Akasaka4, Hiroshi Wada3, Mamiko Yajima1, Gary M Wessel1.   

Abstract

Specification of the germ cell lineage is required for sexual reproduction in all animals. However, the timing and mechanisms of germ cell specification is remarkably diverse in animal development. Echinoderms, such as sea urchins and sea stars, are excellent model systems to study the molecular and cellular mechanisms that contribute to germ cell specification. In several echinoderm embryos tested, the germ cell factor Vasa accumulates broadly during early development and is restricted after gastrulation to cells that contribute to the germ cell lineage. In the sea urchin, however, the germ cell factor Vasa is restricted to a specific lineage by the 32-cell stage. We therefore hypothesized that the germ cell specification program in the sea urchin/Euechinoid lineage has evolved to an earlier developmental time point. To test this hypothesis we determined the expression pattern of a second germ cell factor, Nanos, in four out of five extant echinoderm clades. Here we find that Nanos mRNA does not accumulate until the blastula stage or later during the development of all other echinoderm embryos except those that belong to the Echinoid lineage. Instead, Nanos is expressed in a restricted domain at the 32-128 cell stage in Echinoid embryos. Our results support the model that the germ cell specification program underwent a heterochronic shift in the Echinoid lineage. A comparison of Echinoid and non-Echinoid germ cell specification mechanisms will contribute to our understanding of how these mechanisms have changed during animal evolution.
© 2016 Wiley Periodicals, Inc.

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Year:  2016        PMID: 27402572      PMCID: PMC4943673          DOI: 10.1111/ede.12197

Source DB:  PubMed          Journal:  Evol Dev        ISSN: 1520-541X            Impact factor:   1.930


  49 in total

Review 1.  Use of sea stars to study basic reproductive processes.

Authors:  Gary M Wessel; Adrian M Reich; Peter C Klatsky
Journal:  Syst Biol Reprod Med       Date:  2010-06       Impact factor: 3.061

2.  Germ line determinants are not localized early in sea urchin development, but do accumulate in the small micromere lineage.

Authors:  Celina E Juliano; Ekaterina Voronina; Christie Stack; Maryanna Aldrich; Andrew R Cameron; Gary M Wessel
Journal:  Dev Biol       Date:  2006-08-04       Impact factor: 3.582

3.  The DEAD-box RNA helicase Vasa functions in embryonic mitotic progression in the sea urchin.

Authors:  Mamiko Yajima; Gary M Wessel
Journal:  Development       Date:  2011-04-27       Impact factor: 6.868

Review 4.  Repressive translational control in germ cells.

Authors:  Fangfang Lai; Mary Lou King
Journal:  Mol Reprod Dev       Date:  2013-03-18       Impact factor: 2.609

5.  The Drosophila posterior-group gene nanos functions by repressing hunchback activity.

Authors:  V Irish; R Lehmann; M Akam
Journal:  Nature       Date:  1989-04-20       Impact factor: 49.962

6.  Patterning of anteroposterior body axis displayed in the expression of Hox genes in sea cucumber Apostichopus japonicus.

Authors:  Mani Kikuchi; Akihito Omori; Daisuke Kurokawa; Koji Akasaka
Journal:  Dev Genes Evol       Date:  2015-08-07       Impact factor: 0.900

7.  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

8.  Transplantation of posterior polar plasm in Drosophila. Induction of germ cells at the anterior pole of the egg.

Authors:  K Illmensee; A P Mahowald
Journal:  Proc Natl Acad Sci U S A       Date:  1974-04       Impact factor: 11.205

9.  Development of an embryonic skeletogenic mesenchyme lineage in a sea cucumber reveals the trajectory of change for the evolution of novel structures in echinoderms.

Authors:  Brenna S McCauley; Erin P Wright; Cameron Exner; Chisato Kitazawa; Veronica F Hinman
Journal:  Evodevo       Date:  2012-08-09       Impact factor: 2.250

10.  Phylogenomic analyses of Echinodermata support the sister groups of Asterozoa and Echinozoa.

Authors:  Adrian Reich; Casey Dunn; Koji Akasaka; Gary Wessel
Journal:  PLoS One       Date:  2015-03-20       Impact factor: 3.240

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  3 in total

1.  Nodal induces sequential restriction of germ cell factors during primordial germ cell specification.

Authors:  Tara M Fresques; Gary M Wessel
Journal:  Development       Date:  2018-01-22       Impact factor: 6.868

2.  A tumor suppressor Retinoblastoma1 is essential for embryonic development in the sea urchin.

Authors:  Ana Fernandez-Nicolas; Derek Xu; Mamiko Yajima
Journal:  Dev Dyn       Date:  2019-10-01       Impact factor: 3.780

Review 3.  Conditional specification of endomesoderm.

Authors:  David R McClay; Jenifer C Croce; Jacob F Warner
Journal:  Cells Dev       Date:  2021-07-07
  3 in total

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