[HTML][HTML] D-six4 plays a key role in patterning cell identities deriving from the Drosophila mesoderm

IBN Clark, J Boyd, G Hamilton, DJ Finnegan… - Developmental …, 2006 - Elsevier
IBN Clark, J Boyd, G Hamilton, DJ Finnegan, AP Jarman
Developmental biology, 2006Elsevier
Patterning of the Drosophila embryonic mesoderm requires the regulation of cell type-
specific factors in response to dorsoventral and anteroposterior axis information. For the
dorsoventral axis, the homeodomain gene, tinman, is a key patterning mediator for dorsal
mesodermal fates like the heart. However, equivalent mediators for more ventral fates are
unknown. We show that D-six4, which encodes a Six family transcription factor, is required
for the appropriate development of most cell types deriving from the non-dorsal mesoderm …
Patterning of the Drosophila embryonic mesoderm requires the regulation of cell type-specific factors in response to dorsoventral and anteroposterior axis information. For the dorsoventral axis, the homeodomain gene, tinman, is a key patterning mediator for dorsal mesodermal fates like the heart. However, equivalent mediators for more ventral fates are unknown. We show that D-six4, which encodes a Six family transcription factor, is required for the appropriate development of most cell types deriving from the non-dorsal mesoderm — the fat body, somatic cells of the gonad, and a specific subset of somatic muscles. Misexpression analysis suggests that D-Six4 and its likely cofactor, Eyes absent, are sufficient to impose these fates on other mesodermal cells. At stage 10, the mesodermal expression patterns of D-six4 and tin are complementary, being restricted to the dorsal and non-dorsal regions respectively. Our data suggest that D-six4 is a key mesodermal patterning mediator at this stage that regulates a variety of cell-type-specific factors and hence plays an equivalent role to tin. At stage 9, however, D-six4 and tin are both expressed pan-mesodermally. At this stage, tin function is required for full D-six4 expression. This may explain the known requirement for tin in some non-dorsal cell types.
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