Literature DB >> 10525332

Intracellular fate mapping in a basal metazoan, the ctenophore Mnemiopsis leidyi, reveals the origins of mesoderm and the existence of indeterminate cell lineages.

M Q Martindale1, J Q Henry.   

Abstract

Ctenophores are marine invertebrates that develop rapidly and directly into juvenile adults. They are likely to be the simplest metazoans possessing definitive muscle cells and are possibly the sister group to the Bilateria. All ctenophore embryos display a highly stereotyped, phylum-specific pattern of development in which every cell can be identified by its lineage history. We generated a cell lineage fate map for Mnemiopsis leidyi by injecting fluorescent lineage tracers into individual blastomeres up through the 60-cell stage. The adult ctenophore body plan is composed of four nearly identical quadrants organized along the oral-aboral axis. Each of the four quadrants is derived largely from one cell of the four-cell-stage embryo. At the eight-cell stage each quadrant contains a single E ("end") and M ("middle") blastomere. Subsequently, micromeres are formed first at the aboral pole and later at the oral pole. The ctene rows, apical organ, and tentacle apparatus are complex structures that are generated by both E and M blastomere lineages from all four quadrants. All muscle cells are derived from micromeres born at the oral pole of endomesodermal precursors (2M and 3E macromeres). While the development of the four quadrants is similar, diagonally opposed quadrants share more similarities than adjacent quadrants. Adult ctenophores possess two diagonally opposed endodermal anal canals that open at the base of the apical organ. These two structures are derived from the two diagonally opposed 2M/ macromeres. The two opposing 2M/ macromeres generated a unique set of circumpharyngeal muscle cells, but do not contribute to the anal canals. No other lineages displayed such diagonal asymmetries. Clones from each blastomere yielded regular, but not completely invariant patterns of descendents. Ectodermal descendents normally, but not always, remained within their corresponding quadrants. On the other hand, endodermal and mesodermal progeny dispersed throughout the body. The variability in the exact complements of adult structures, along with previously published cell deletion experiments, demonstrates that cell interactions are required for normal cell fate determination. Ctenophore embryos, like those of many bilaterian phyla (e.g., spiralians, nematodes, and echinoids), display a highly stereotyped cleavage program in which some, but not all, blastomeres are determined at the time of their birth. The results suggest that mesodermal tissues originally evolved from endoderm tissue. Copyright 1999 Academic Press.

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Year:  1999        PMID: 10525332     DOI: 10.1006/dbio.1999.9427

Source DB:  PubMed          Journal:  Dev Biol        ISSN: 0012-1606            Impact factor:   3.582


  26 in total

Review 1.  From nerve net to nerve ring, nerve cord and brain--evolution of the nervous system.

Authors:  Detlev Arendt; Maria Antonietta Tosches; Heather Marlow
Journal:  Nat Rev Neurosci       Date:  2016-01       Impact factor: 34.870

2.  Gut-like ectodermal tissue in a sea anemone challenges germ layer homology.

Authors:  Patrick R H Steinmetz; Andy Aman; Johanna E M Kraus; Ulrich Technau
Journal:  Nat Ecol Evol       Date:  2017-09-11       Impact factor: 15.460

3.  The genome of the ctenophore Mnemiopsis leidyi and its implications for cell type evolution.

Authors:  Joseph F Ryan; Kevin Pang; Christine E Schnitzler; Anh-Dao Nguyen; R Travis Moreland; David K Simmons; Bernard J Koch; Warren R Francis; Paul Havlak; Stephen A Smith; Nicholas H Putnam; Steven H D Haddock; Casey W Dunn; Tyra G Wolfsberg; James C Mullikin; Mark Q Martindale; Andreas D Baxevanis
Journal:  Science       Date:  2013-12-13       Impact factor: 47.728

4.  The maternal-zygotic transition and zygotic activation of the Mnemiopsis leidyi genome occurs within the first three cleavage cycles.

Authors:  Phillip L Davidson; Bernard J Koch; Christine E Schnitzler; Jonathan Q Henry; Mark Q Martindale; Andreas D Baxevanis; William E Browne
Journal:  Mol Reprod Dev       Date:  2017-11-10       Impact factor: 2.609

5.  Molecular architecture of muscles in an acoel and its evolutionary implications.

Authors:  Marta Chiodin; Johannes G Achatz; Andreas Wanninger; Pedro Martinez
Journal:  J Exp Zool B Mol Dev Evol       Date:  2011-05-02       Impact factor: 2.656

6.  A comprehensive fate map by intracellular injection of identified blastomeres in the marine polychaete Capitella teleta.

Authors:  Néva P Meyer; Michael J Boyle; Mark Q Martindale; Elaine C Seaver
Journal:  Evodevo       Date:  2010-09-15       Impact factor: 2.250

7.  Ancient connection between NKL genes and the mesoderm? Insights from Tlx expression in a ctenophore.

Authors:  Romain Derelle; Michaël Manuel
Journal:  Dev Genes Evol       Date:  2007-02-07       Impact factor: 0.900

8.  Independent specialisation of myosin II paralogues in muscle vs. non-muscle functions during early animal evolution: a ctenophore perspective.

Authors:  Cyrielle Dayraud; Alexandre Alié; Muriel Jager; Patrick Chang; Hervé Le Guyader; Michaël Manuel; Eric Quéinnec
Journal:  BMC Evol Biol       Date:  2012-07-02       Impact factor: 3.260

Review 9.  Whole-Body Regeneration in the Lobate Ctenophore Mnemiopsis leidyi.

Authors:  Allison Edgar; Dorothy G Mitchell; Mark Q Martindale
Journal:  Genes (Basel)       Date:  2021-06-05       Impact factor: 4.096

10.  A diploblastic radiate animal at the dawn of cambrian diversification with a simple body plan: distinct from Cnidaria?

Authors:  Kinya Yasui; James D Reimer; Yunhuan Liu; Xiaoyong Yao; Daisuke Kubo; Degan Shu; Yong Li
Journal:  PLoS One       Date:  2013-06-20       Impact factor: 3.240

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