Abstract

Developmental processes are highly dependent on transcriptional regulation by RNA polymerase II. The RNA polymerase II core promoter is the ultimate target of a multitude of transcription factors that control transcription initiation. Core promoters consist of core promoter motifs, e.g. the initiator, TATA box, and the downstream core promoter element (DPE), which confer specific properties to the core promoter. Here, we explored the importance of core promoter functions in the dorsal-ventral developmental gene regulatory network. This network includes multiple genes that are activated by different nuclear concentrations of Dorsal, an NFκB homolog transcription factor, along the dorsal-ventral axis. We show that over two-thirds of Dorsal target genes contain DPE sequence motifs, which is significantly higher than the proportion of DPE-containing promoters in Drosophila genes. We demonstrate that multiple Dorsal target genes are evolutionarily conserved and functionally dependent on the DPE. Furthermore, we have analyzed the activation of key Dorsal target genes by Dorsal, as well as by another Rel family transcription factor, Relish, and the dependence of their activation on the DPE motif. Using hybrid enhancer-promoter constructs in Drosophila cells and embryo extracts, we have demonstrated that the core promoter composition is an important determinant of transcriptional activity of Dorsal target genes. Taken together, our results provide evidence for the importance of core promoter composition in the regulation of Dorsal target genes.

Highlights

  • The Dorsal transcription factor regulates the dorsal-ventral developmental gene regulatory network by binding to enhancers

  • Identification of downstream core promoter element (DPE) Motifs in Core Promoters of Dorsal Target Genes—To discover distinct gene regulatory networks (GRNs) and pathways that are regulated via the core promoter, we have examined the core promoter composition of genes that are involved in early embryonic fly development

  • The DPE Motif in Multiple Drosophila Dorsal Target Genes Is Conserved—To examine whether core promoter elements play a role in the regulation of Dorsal-target gene expression, we have analyzed the sequence conservation of Dorsal target genes that are activated by different nuclear concentration of Dorsal: mesodermal genes that are activated by the highest concentrations of Dorsal, namely tinman, twist, phantom, rho-like (RhoL; Mes1), and Multi drug resistance 49 (Mdr49; Mes5) [45, 47, 55,56,57,58], neurogenic ectoderm genes that

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Summary

Background

The Dorsal transcription factor regulates the dorsal-ventral developmental gene regulatory network by binding to enhancers. Multiple sequence-specific DNA binding transcription factors and co-regulators control gene expression [7,8,9,10], but the ultimate target of the transcrip-. The DPE was originally discovered as a TFIID recognition site that is located downstream of the initiator element (precisely from ϩ28 to ϩ33 relative to the Aϩ1 of the Inr) and is conserved from Drosophila to humans [27, 28]. It is bound by the TAF6 and TAF9 subunits of TFIID [28]. We have previously demonstrated that gene expression levels can be modulated via the core promoter [31]

The abbreviations used are
EXPERIMENTAL PROCEDURES
RESULTS
C Dorsal binding site
DISCUSSION
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