Schulte-Merker_1994_Development_120_1009

Reference

Title : no tail (ntl) is the zebrafish homologue of the mouse T (Brachyury) gene - Schulte-Merker_1994_Development_120_1009
Author(s) : Schulte-Merker S , van Eeden FJ , Halpern ME , Kimmel CB , Nusslein-Volhard C
Ref : Development , 120 :1009 , 1994
Abstract :

The mouse T (Brachyury) gene is required for normal mesoderm development and the extension of the body axis. Recently, two mutant alleles of a zebrafish gene, no tail (ntl), have been isolated (Halpern, M. E., Ho., R. K., Walker, C. and Kimmel, C. B. (1993) Cell 75, 99-111). ntl mutant embryos resemble mouse T/T mutant embryos in that they lack a differentiated notochord and the caudal region of their bodies. We report here that this phenotype is caused by mutation of the zebrafish homologue of the T gene. While ntl embryos express mutant mRNA, they show no nuclear protein product. Later, expression of mRNA in mutants, but not in wild types, is greatly reduced along the dorsal midline where the notochord normally forms. This suggests that the protein is required for maintaining transcription of its own gene.

PubMedSearch : Schulte-Merker_1994_Development_120_1009
PubMedID: 7600949

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Citations formats

Schulte-Merker S, van Eeden FJ, Halpern ME, Kimmel CB, Nusslein-Volhard C (1994)
no tail (ntl) is the zebrafish homologue of the mouse T (Brachyury) gene
Development 120 :1009

Schulte-Merker S, van Eeden FJ, Halpern ME, Kimmel CB, Nusslein-Volhard C (1994)
Development 120 :1009