A Database of Drosophila Genes & Genomes

FB2013_03, released May 7th, 2013
 

Reference Report

Reference
Citation Wiklund, M.L., Steinert, S., Junell, A., Hultmark, D., Stöven, S. (2009). The N-terminal half of the Drosophila Rel/NF-kappaB factor Relish, REL-68, constitutively activates transcription of specific Relish target genes.  Dev. Comp. Immunol. 33(5): 690--696. (Export to RIS)
FlyBase ID FBrf0207341
Publication Type Research paper
PubMed ID 19135474
PubMed Abstract The Rel/NF-kappaB transcription factor Relish is a major regulator of the antimicrobial response in Drosophila. Upon immune challenge, Relish is cleaved to generate two fragments, the DNA-binding transcription factor REL-68 and the IkappaB-like REL-49. Using transgenic fly strains we show here that overexpression of REL-68 separately from REL-49 is sufficient to activate strong constitutive transcription of the Diptericin gene, but little constitutive or inducible transcription of Attacin and Cecropin, two other Relish target genes. Their transcription may therefore require additional modifications of Relish. However, phosphorylation of the conserved serine residue S431 is not involved in such modifications. This is unlike p65 and Dorsal, which are modulated by phosphorylation at their homologous site. In contrast to other IkappaB proteins, overexpression of REL-49 had no inhibitory effect on Relish-dependent transcription. Instead, we propose that the C-terminal IkappaB-like domain executes a scaffolding and recruiting function for full activation of Relish.
DOI 10.1016/j.dci.2008.12.002
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Language of Publication English
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Publication Type Journal
Abbreviation Dev. Comp. Immunol.
Title Developmental and Comparative Immunology
Publication Year 1977-
ISBN/ISSN 0145-305X
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