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Pax-Six-Eya-Dach network during amphioxus development: conservation in vitro but context specificity in vivo
Kozmik Z., Holland N.D., Kreslova J., Oliveri D., Schubert M., Jonasova K., Holland L.Z., Pestarino M., Benes V., Candiani S.
Language English Country United States
NLK
Free Medical Journals
from 1959 to 1 year ago
- MeSH
- Pituitary Gland, Anterior metabolism growth & development MeSH
- Active Transport, Cell Nucleus MeSH
- Central Nervous System metabolism growth & development MeSH
- Chordata genetics growth & development MeSH
- Epidermal Cells MeSH
- Epidermis growth & development MeSH
- Gene Expression MeSH
- Financing, Organized MeSH
- Phylogeny MeSH
- Homeodomain Proteins analysis genetics metabolism MeSH
- Kidney metabolism growth & development MeSH
- RNA, Messenger analysis metabolism MeSH
- Neurons, Afferent metabolism MeSH
- Nerve Tissue Proteins analysis genetics metabolism MeSH
- Animals MeSH
- Check Tag
- Animals MeSH
The Drosophila retinal determination gene network occurs in animals generally as a Pax-Six-Eyes absent-Dachshund network (PSEDN). For amphioxus, we describe the complete network of nine PSEDN genes, four of which-AmphiSix1/2, AmphiSix4/5, AmphSix3/6, and AmphiEya-are characterized here for the first time. For amphioxus, in vitro interactions among the genes and proteins of the network resemble those of other animals, except for the absence of Dach-Eya binding. Amphioxus PSEDN genes are expressed in highly stage- and tissue-specific patterns (sometimes conspicuously correlated with the local intensity of cell proliferation) in the gastrular organizer, notochord, somites, anterior central nervous system, peripheral nervous system, pharyngeal endoderm, and the likely homolog of the vertebrate adenohypophysis. In this last tissue, the anterior region expresses all three amphioxus Six genes and is a zone of active cell proliferation, while the posterior region expresses only AmphiPax6 and is non-proliferative. In summary, the topologies of animal PSEDNs, although considerably more variable than originally proposed, are conserved enough to be recognizable among species and among developing tissues; this conservation may reflect indispensable involvement of PSEDNs during the critically important early phases of embryology (e.g. in the control of mitosis, apoptosis, and cell/tissue motility).
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- $a Institute of Molecular Genetics, Videnska 1083, 14220 Prague 4, Czech Republic
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