Literature DB >> 2878844

The ontogeny and maintenance of adult symmetry properties in the ctenophore, Mnemiopsis mccradyi.

M Q Martindale.   

Abstract

Ctenophores are biradially symmetrical animals. The body is composed of four identical quadrants which are organized along an oral-aboral axis. Most species have eight comb rows, two tentacles, and an apical organ (located on the aboral surface). During embryogenesis there is a fixed pattern of cleavage, a precocious specification of blastomere developmental potential, and an inability to regulate for portions of the embryo that have been removed. When blastomeres are separated at the two-cell stage each blastomere develops into a "half-animal" with four comb rows, one tentacle, and half an apical organ. In contrast, adult ctenophores regenerate readily. When an adult ctenophore is cut in half to produce "half-animals," in most cases each half regenerates the missing half. In some cases, however, bisected animals remain as "half-animals" which repair the wound site but do not replace all of the missing structures. When animals are cut in half along the tentacular or esophageal axis at different stages of embryogenesis a transition period is detected when the capacity for adult regeneration begins. This transition occurs at the time when the formation of the apical organ is complete and comb row function becomes coordinated. Embryos bisected prior to this time remain as "half-animals" even after growing to large reproductive sizes, while animals bisected after the transition period usually regenerate the missing structures within 2-3 days. When adult "half-animals" (produced by bisection either before or after the transition period) are cut into "quarter-pieces," the pieces regenerate to form either "half-animals" or whole animals. Thus, "half-animals" produced prior to the transition period--although they failed to undergo embryonic regulation--have not irreversibly lost the capacity to form whole animals if challenged to regenerate during adult stages. When aboral blastomeres destined to form the apical organ, tentacles, and comb rows are removed from early cleavage stages (prior to the transition period), the embryo does not form these structures at the appropriate time. However, the resulting deficient adults spontaneously form these structures from remaining blastomere lineages soon after hatching. These experiments suggest that as long as some quadrant-specific cells of the oral pole are present at the time of the transition period, the structures of that quadrant will be spontaneously replaced during the adult period.(ABSTRACT TRUNCATED AT 400 WORDS)

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Year:  1986        PMID: 2878844     DOI: 10.1016/0012-1606(86)90026-6

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


  10 in total

Review 1.  Multigenerational laboratory culture of pelagic ctenophores and CRISPR-Cas9 genome editing in the lobate Mnemiopsis leidyi.

Authors:  J S Presnell; W E Browne; M Bubel; T Knowles; W Patry
Journal:  Nat Protoc       Date:  2022-06-13       Impact factor: 17.021

2.  Studying Ctenophora WBR Using Mnemiopsis leidyi.

Authors:  Julia Ramon-Mateu; Allison Edgar; Dorothy Mitchell; Mark Q Martindale
Journal:  Methods Mol Biol       Date:  2022

3.  A cleavage clock regulates features of lineage-specific differentiation in the development of a basal branching metazoan, the ctenophore Mnemiopsis leidyi.

Authors:  Antje Hl Fischer; Kevin Pang; Jonathan Q Henry; Mark Q Martindale
Journal:  Evodevo       Date:  2014-01-31       Impact factor: 2.250

4.  Developmental expression of "germline"- and "sex determination"-related genes in the ctenophore Mnemiopsis leidyi.

Authors:  Adam M Reitzel; Kevin Pang; Mark Q Martindale
Journal:  Evodevo       Date:  2016-08-02       Impact factor: 2.250

5.  Food availability drives plastic self-repair response in a basal metazoan- case study on the ctenophore Mnemiopsis leidyi A. Agassiz 1865.

Authors:  Katharina Tissy Bading; Sarah Kaehlert; Xupeng Chi; Cornelia Jaspers; Mark Q Martindale; Jamileh Javidpour
Journal:  Sci Rep       Date:  2017-11-27       Impact factor: 4.379

6.  Regeneration in the ctenophore Mnemiopsis leidyi occurs in the absence of a blastema, requires cell division, and is temporally separable from wound healing.

Authors:  Julia Ramon-Mateu; S Tori Ellison; Thomas E Angelini; Mark Q Martindale
Journal:  BMC Biol       Date:  2019-10-11       Impact factor: 7.431

Review 7.  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

8.  Genomic organization, evolution, and expression of photoprotein and opsin genes in Mnemiopsis leidyi: a new view of ctenophore photocytes.

Authors:  Christine E Schnitzler; Kevin Pang; Meghan L Powers; Adam M Reitzel; Joseph F Ryan; David Simmons; Takashi Tada; Morgan Park; Jyoti Gupta; Shelise Y Brooks; Robert W Blakesley; Shozo Yokoyama; Steven Hd Haddock; Mark Q Martindale; Andreas D Baxevanis
Journal:  BMC Biol       Date:  2012-12-21       Impact factor: 7.431

9.  Expression of multiple Sox genes through embryonic development in the ctenophore Mnemiopsis leidyi is spatially restricted to zones of cell proliferation.

Authors:  Christine E Schnitzler; David K Simmons; Kevin Pang; Mark Q Martindale; Andreas D Baxevanis
Journal:  Evodevo       Date:  2014-04-24       Impact factor: 2.250

10.  Integrating Embryonic Development and Evolutionary History to Characterize Tentacle-Specific Cell Types in a Ctenophore.

Authors:  Leslie S Babonis; Melissa B DeBiasse; Warren R Francis; Lynne M Christianson; Anthony G Moss; Steven H D Haddock; Mark Q Martindale; Joseph F Ryan
Journal:  Mol Biol Evol       Date:  2018-12-01       Impact factor: 16.240

  10 in total

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