Literature DB >> 21177341

Small micromeres contribute to the germline in the sea urchin.

Mamiko Yajima1, Gary M Wessel.   

Abstract

Many indirect developing animals create specialized multipotent cells in early development to construct the adult body and perhaps to hold the fate of the primordial germ cells. In sea urchin embryos, small micromeres formed at the fifth division appear to be such multipotent cells: they are relatively quiescent in embryos, but contribute significantly to the coelomic sacs of the larvae, from which the major tissues of the adult rudiment are derived. These cells appear to be regulated by a conserved gene set that includes the classic germline lineage genes vasa, nanos and piwi. In vivo lineage mapping of the cells awaits genetic manipulation of the lineage, but previous research has demonstrated that the germline is not specified at the fourth division because animals are fertile even when micromeres, the parent blastomeres of small micromeres, are deleted. Here, we have deleted small micromeres at the fifth division and have raised the resultant larvae to maturity. These embryos developed normally and did not overexpress Vasa, as did embryos from a micromere deletion, implying the compensatory gene regulatory network was not activated in small micromere-deleted embryos. Adults from control and micromere-deleted embryos developed gonads and visible gametes, whereas small micromere-deleted animals formed small gonads that lacked gametes. Quantitative PCR results indicate that small micromere-deleted animals produce background levels of germ cell products, but not specifically eggs or sperm. These results suggest that germline specification depends on the small micromeres, either directly as lineage products, or indirectly by signaling mechanisms emanating from the small micromeres or their descendants.

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Year:  2011        PMID: 21177341      PMCID: PMC3005600          DOI: 10.1242/dev.054940

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


  41 in total

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Review 2.  Mechanisms of germ cell specification across the metazoans: epigenesis and preformation.

Authors:  Cassandra G Extavour; Michael Akam
Journal:  Development       Date:  2003-12       Impact factor: 6.868

3.  Nanos maintains germline stem cell self-renewal by preventing differentiation.

Authors:  Zhong Wang; Haifan Lin
Journal:  Science       Date:  2004-02-19       Impact factor: 47.728

4.  A conserved germline multipotency program.

Authors:  Celina E Juliano; S Zachary Swartz; Gary M Wessel
Journal:  Development       Date:  2010-12       Impact factor: 6.868

5.  Developmental biology. Versatile germline genes.

Authors:  Celina Juliano; Gary Wessel
Journal:  Science       Date:  2010-08-06       Impact factor: 47.728

Review 6.  The function and regulation of vasa-like genes in germ-cell development.

Authors:  E Raz
Journal:  Genome Biol       Date:  2000-09-01       Impact factor: 13.583

7.  The mouse homolog of Drosophila Vasa is required for the development of male germ cells.

Authors:  S S Tanaka; Y Toyooka; R Akasu; Y Katoh-Fukui; Y Nakahara; R Suzuki; M Yokoyama; T Noce
Journal:  Genes Dev       Date:  2000-04-01       Impact factor: 11.361

8.  Regulation of Drosophila vasa in vivo through paralogous cullin-RING E3 ligase specificity receptors.

Authors:  Jan-Michael Kugler; Jae-Sung Woo; Byung-Ha Oh; Paul Lasko
Journal:  Mol Cell Biol       Date:  2010-02-01       Impact factor: 4.272

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.  Conserved role of nanos proteins in germ cell development.

Authors:  Masayuki Tsuda; Yumiko Sasaoka; Makoto Kiso; Kuniya Abe; Seiki Haraguchi; Satoru Kobayashi; Yumiko Saga
Journal:  Science       Date:  2003-08-29       Impact factor: 47.728

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  44 in total

Review 1.  Germ Line Versus Soma in the Transition from Egg to Embryo.

Authors:  S Zachary Swartz; Gary M Wessel
Journal:  Curr Top Dev Biol       Date:  2015-08-19       Impact factor: 4.897

2.  Programmed reduction of ABC transporter activity in sea urchin germline progenitors.

Authors:  Joseph P Campanale; Amro Hamdoun
Journal:  Development       Date:  2012-02       Impact factor: 6.868

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.  Evolutionary crossroads in developmental biology: sea urchins.

Authors:  David R McClay
Journal:  Development       Date:  2011-07       Impact factor: 6.868

5.  Isolating specific embryonic cells of the sea urchin by FACS.

Authors:  Celina Juliano; S Zachary Swartz; Gary Wessel
Journal:  Methods Mol Biol       Date:  2014

6.  Essential elements for translation: the germline factor Vasa functions broadly in somatic cells.

Authors:  Mamiko Yajima; Gary M Wessel
Journal:  Development       Date:  2015-05-14       Impact factor: 6.868

Review 7.  Methods to label, isolate, and image sea urchin small micromeres, the primordial germ cells (PGCs).

Authors:  Joseph P Campanale; Amro Hamdoun; Gary M Wessel; Yi-Hsien Su; Nathalie Oulhen
Journal:  Methods Cell Biol       Date:  2019-01-08       Impact factor: 1.441

8.  ISWI contributes to ArsI insulator function in development of the sea urchin.

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

9.  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

10.  Piwi regulates Vasa accumulation during embryogenesis in the sea urchin.

Authors:  Mamiko Yajima; Eric A Gustafson; Jia L Song; Gary M Wessel
Journal:  Dev Dyn       Date:  2014-03       Impact factor: 3.780

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