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Mol. Cell. Biol., Aug 1997, 4355-4362, Vol 17, No. 8
G Jimenez and D Ish-Horowicz
Drosophila melanogaster neurogenesis requires the opposing activities of
two sets of basic helix-loop-helix (bHLH) proteins: proneural proteins,
which confer on cells the ability to become neural precursors, and the
Enhancer-of-split [E(spl)] proteins, which restrict such potential as part
of the lateral inhibition process. Here, we test if E(spl) proteins
function as promoter-bound repressors by examining the effects on
neurogenesis of an E(spl) derivative containing a heterologous
transcriptional activation domain [E(spl) m7Act (m7Act)]. In contrast to
the wild-type E(spl) proteins, m7Act efficiently induces neural
development, indicating that it binds to and activates target genes
normally repressed by E(spl). Mutations in the basic domain disrupt m7Act
activity, suggesting that its effects are mediated through direct DNA
binding. m7Act causes ectopic transcription of the proneural achaete and
scute genes. Our results support a model in which E(spl) proteins normally
regulate neurogenesis by direct repression of genes at the top of the
neural determination pathway.
Copyright © 1997, American Society for Microbiology
A chimeric enhancer-of-split transcriptional activator drives neural development and achaete-scute expression
Imperial Cancer Research Fund, London, England.
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