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Submitted on September 26, 2003
Accepted on February 17, 2004
Max-Planck Institute for Immunobiology, Stuebeweg 51, 79108 Freiburg, Germany
* To whom correspondence should be addressed. E-mail: hammerschmid{at}immunbio.mpg.de.
The Pou domain transcription factor Pit-1 is required for lineage determination and cellular commitment processes during mammalian adenohypophysis development. Here we report the cloning and mutational analysis of a pit1 homologue from zebrafish. Compared with mouse, zebrafish pit1 starts to be expressed at a much earlier stage of adenohypophysis development. However, like in mouse, expression is restricted to a subset of pituitary cell types, excluding proopiomelanocortin (pomc)-expressing cells (corticotropes, melanotropes) and possibly gonadotropes. We could identify two ENU-induced zebrafish pit1 null mutants. Most mutants die during larval stages, while survivors develop severe dwarfism. Mutant larvae lack lactotropes, somatotropes and thyrotropes, although the adenohypophysis is of normal size, without any sign of increased apoptosis rates. Instead, mutant embryos initiate ectopic expression of pomc in pit1-positive cells, leading to an expansion of the Pomc lineage. Similarly, the number of gonadotropes seems increased, as indicated by the expression of gsu
, a marker for thyrotropes and gonadotropes. In pit1 mutants, the total number of gsu-positive cells is normal despite the loss of gsu and tsh
co-expressing cells. Together, these data suggest a transfating of the Pit1 lineage to the Pomc and possibly the gonadotroph lineages in the mutant, and a pomc- and gonadotropin-repressive role of Pit1 during normal zebrafish development. This is different from mouse, for which a repressive role of Pit-1 has only been reported for the gonadotropin Lh, but not for Pomc. In sum, our data point to both conserved and class-specific aspects of Pit1 function during pituitary development in different vertebrate species.
•
zebrafish •
adenohypophysis •
pituitary •
ENU •
mutant •
Growth hormone •
Prolactin •
Tsh •
Proopiomelanocortin
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