Brachyury null mutant-induced defects in juvenile ascidian endodermal organs.

TitleBrachyury null mutant-induced defects in juvenile ascidian endodermal organs.
Publication TypeJournal Article
Year of Publication2009
AuthorsChiba S, Jiang D, Satoh N, Smith WC
JournalDevelopment
Volume136
Issue1
Pagination35-9
Date Published2009 Jan
ISSN0950-1991
KeywordsAmino Acid Sequence, Animals, Base Sequence, Biological Markers, Cell Lineage, Ciona intestinalis, DNA Mutational Analysis, Endoderm, Ethylnitrosourea, Fetal Proteins, Gastrointestinal Tract, Metamorphosis, Biological, Molecular Sequence Data, Mutation, Notochord, Organ Specificity, T-Box Domain Proteins, Tail
Abstract

We report the isolation of a recessive ENU-induced short-tailed mutant in the ascidian Ciona intestinalis that is the product of a premature stop in the brachyury gene. Notochord differentiation and morphogenesis are severely disrupted in the mutant line. At the larval stage, variable degrees of ectopic endoderm staining were observed in the homozygous mutants, indicating that loss of brachyury results in stochastic fate transformation. In post-metamorphosis mutants, a uniform defect in tail resorption was observed, together with variable defects in digestive tract development. Some cells misdirected from the notochord lineage were found to be incorporated into definitive endodermal structures, such as stomach and intestine.

DOI10.1242/dev.030981
Alternate JournalDevelopment
PubMed ID19019990
PubMed Central IDPMC2685961
Grant ListGM075049 / GM / NIGMS NIH HHS / United States
HD38701 / HD / NICHD NIH HHS / United States