Literature DB >> 10851130

An FGF signal from endoderm and localized factors in the posterior-vegetal egg cytoplasm pattern the mesodermal tissues in the ascidian embryo.

G J Kim1, A Yamada, H Nishida.   

Abstract

The major mesodermal tissues of ascidian larvae are muscle, notochord and mesenchyme. They are derived from the marginal zone surrounding the endoderm area in the vegetal hemisphere. Muscle fate is specified by localized ooplasmic determinants, whereas specification of notochord and mesenchyme requires inducing signals from endoderm at the 32-cell stage. In the present study, we demonstrated that all endoderm precursors were able to induce formation of notochord and mesenchyme cells in presumptive notochord and mesenchyme blastomeres, respectively, indicating that the type of tissue induced depends on differences in the responsiveness of the signal-receiving blastomeres. Basic fibroblast growth factor (bFGF), but not activin A, induced formation of mesenchyme cells as well as notochord cells. Treatment of mesenchyme-muscle precursors isolated from early 32-cell embryos with bFGF promoted mesenchyme fate and suppressed muscle fate, which is a default fate assigned by the posterior-vegetal cytoplasm (PVC) of the eggs. The sensitivity of the mesenchyme precursors to bFGF reached a maximum at the 32-cell stage, and the time required for effective induction of mesenchyme cells was only 10 minutes, features similar to those of notochord induction. These results support the idea that the distinct tissue types, notochord and mesenchyme, are induced by the same signaling molecule originating from endoderm precursors. We also demonstrated that the PVC causes the difference in the responsiveness of notochord and mesenchyme precursor blastomeres. Removal of the PVC resulted in loss of mesenchyme and in ectopic notochord formation. In contrast, transplantation of the PVC led to ectopic formation of mesenchyme cells and loss of notochord. Thus, in normal development, notochord is induced by an FGF-like signal in the anterior margin of the vegetal hemisphere, where PVC is absent, and mesenchyme is induced by an FGF-like signal in the posterior margin, where PVC is present. The whole picture of mesodermal patterning in ascidian embryos is now known. We also discuss the importance of FGF induced asymmetric divisions, of notochord and mesenchyme precursor blastomeres at the 64-cell stage.

Entities:  

Mesh:

Substances:

Year:  2000        PMID: 10851130     DOI: 10.1242/dev.127.13.2853

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


  13 in total

1.  Cleavage-arrested cell triplets from ascidian embryo differentiate into three cell types depending on cell combination and contact timing.

Authors:  Motoko Tanaka-Kunishima; Kunitaro Takahashi
Journal:  J Physiol       Date:  2002-04-01       Impact factor: 5.182

2.  Evolutionary origins of the vertebrate heart: Specification of the cardiac lineage in Ciona intestinalis.

Authors:  Brad Davidson; Michael Levine
Journal:  Proc Natl Acad Sci U S A       Date:  2003-09-18       Impact factor: 11.205

3.  Muscle development in Ciona intestinalis requires the b-HLH myogenic regulatory factor gene Ci-MRF.

Authors:  Thomas H Meedel; Patrick Chang; Hitoyoshi Yasuo
Journal:  Dev Biol       Date:  2006-09-29       Impact factor: 3.582

Review 4.  Ascidian notochord morphogenesis.

Authors:  Di Jiang; William C Smith
Journal:  Dev Dyn       Date:  2007-07       Impact factor: 3.780

5.  The functional analysis of Type I postplasmic/PEM mRNAs in embryos of the ascidian Halocynthia roretzi.

Authors:  Yoriko Nakamura; Kazuhiro W Makabe; Hiroki Nishida
Journal:  Dev Genes Evol       Date:  2005-12-21       Impact factor: 0.900

6.  FGF signaling induces mesoderm in the hemichordate Saccoglossus kowalevskii.

Authors:  Stephen A Green; Rachael P Norris; Mark Terasaki; Christopher J Lowe
Journal:  Development       Date:  2013-01-23       Impact factor: 6.868

7.  Temporal regulation of the muscle gene cascade by Macho1 and Tbx6 transcription factors in Ciona intestinalis.

Authors:  Jamie E Kugler; Stefan Gazdoiu; Izumi Oda-Ishii; Yale J Passamaneck; Albert J Erives; Anna Di Gregorio
Journal:  J Cell Sci       Date:  2010-07-15       Impact factor: 5.285

8.  FGF3 in the floor plate directs notochord convergent extension in the Ciona tadpole.

Authors:  Weiyang Shi; Sara M Peyrot; Edwin Munro; Michael Levine
Journal:  Development       Date:  2008-11-26       Impact factor: 6.868

9.  Nodal signaling is required for mesodermal and ventral but not for dorsal fates in the indirect developing hemichordate, Ptychodera flava.

Authors:  Eric Röttinger; Timothy Q DuBuc; Aldine R Amiel; Mark Q Martindale
Journal:  Biol Open       Date:  2015-05-15       Impact factor: 2.422

10.  Raman spectroscopic imaging of the whole Ciona intestinalis embryo during development.

Authors:  Mitsuru J Nakamura; Kohji Hotta; Kotaro Oka
Journal:  PLoS One       Date:  2013-08-20       Impact factor: 3.240

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.