TINMAN AND BAGPIPE - 2 HOMEO BOX GENES THAT DETERMINE CELL FATES IN THE DORSAL MESODERM OF DROSOPHILA

Citation
N. Azpiazu et M. Frasch, TINMAN AND BAGPIPE - 2 HOMEO BOX GENES THAT DETERMINE CELL FATES IN THE DORSAL MESODERM OF DROSOPHILA, Genes & development, 7(7B), 1993, pp. 1325-1340
Citations number
58
Categorie Soggetti
Developmental Biology","Genetics & Heredity
Journal title
ISSN journal
08909369
Volume
7
Issue
7B
Year of publication
1993
Pages
1325 - 1340
Database
ISI
SICI code
0890-9369(1993)7:7B<1325:TAB-2H>2.0.ZU;2-C
Abstract
Whereas the mechanisms of early Drosophila mesoderm formation have bee n studied in much detail, the subsequent processes determining regiona l identities within the mesoderm remain largely unknown. Here, we desc ribe two homeo box genes, tinman (tin) and bagpipe (bap), which spatia lly subdivide the mesoderm and determine cell fates in the dorsal meso derm. These two genes are components of a cascade of genetic interacti ons that result in the spatial restriction of tin mRNA to the dorsal m esoderm and in the activation of bap in segmental clusters of cells in this region. A subset of cells from those clusters segregate to form visceral mesoderm that differentiates into gut musculature. This indic ates that the visceral mesoderm is derived from metamerically repeated primordia. In embryos mutant for bap, visceral mesoderm formation is strongly disrupted. Most cells of the visceral mesoderm fail to differ entiate properly, and a portion of them are transformed into body wall musculature and gonadal mesoderm. In tin mutant embryos, bap expressi on is not activated in the dorsal mesoderm. Probably as a consequence, neither visceral mesoderm nor midgut musculature are formed in these mutants, and the absence of visceral mesoderm results in strong disrup tions of endoderm migration and midgut morphogenesis. In addition to v isceral mesoderm development, tin is required for the formation of the heart from dorsal mesoderm and for the specification of founder cells for particular body wall muscles.