SAP18, a highly evolutionarily conserved protein, has been proposed to be involved in multiple cellular processes, from gene regulation to mRNA processing. To gain further insight into the role of SAP18, we performed genome-wide expression profiling of dsap18 mutant Drosophila melanogaster embryos and we found that dSAP18 is required for the expression of immune and stress related genes. We show that dSAP18 colocalizes with histone H3 phosphorylation, which has been implicated in the regulation of genes in response to signaling stimuli. dsap18 mutant larvae develop melanotic tumors after heat shock and the viability of dsap18 mutant flies is reduced after fungal infection or in high-salt medium. Altogether, our results indicate that dSAP18 is a key player in transcriptional responses to stress.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1016/j.febslet.2010.11.058 | DOI Listing |
FEBS Lett
January 2011
Institut de Biologia Molecular de Barcelona, CSIC, Barcelona, Spain.
SAP18, a highly evolutionarily conserved protein, has been proposed to be involved in multiple cellular processes, from gene regulation to mRNA processing. To gain further insight into the role of SAP18, we performed genome-wide expression profiling of dsap18 mutant Drosophila melanogaster embryos and we found that dSAP18 is required for the expression of immune and stress related genes. We show that dSAP18 colocalizes with histone H3 phosphorylation, which has been implicated in the regulation of genes in response to signaling stimuli.
View Article and Find Full Text PDFNucleic Acids Res
September 2005
Departament de Biologia Molecular i Cel.lular, Institut de Biologia Molecular de Barcelona, CSIC Parc Científic de Barcelona, Josep Samitier, 1-5 08028 Barcelona, Spain.
It was described earlier that the Drosophila GAGA factor [Trithorax-like (Trl)] interacts with dSAP18, which, in mammals, was reported to be a component of the Sin3-HDAC co-repressor complex. GAGA-dSAP18 interaction was proposed to contribute to the functional regulation of the bithorax complex (BX-C). Here, we show that mutant alleles of Trl, dsap18 and drpd3/hdac1 enhance A6-to-A5 transformation indicating a contribution to the regulation of Abd-B expression at A6.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!