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COP9 signalosome subunits 4 and 5 regulate multiple pleiotropic pathways inDrosophila melanogaster

Authors: Efrat, Oron; Mattias, Mannervik; Sigal, Rencus; Orit, Harari-Steinberg; Shira, Neuman-Silberberg; Daniel, Segal; Daniel A, Chamovitz;

COP9 signalosome subunits 4 and 5 regulate multiple pleiotropic pathways inDrosophila melanogaster

Abstract

The COP9 signalosome (CSN) is an essential eight-subunit repressor of light-regulated development in Arabidopsis. This complex has also been identified in animals, though its developmental role remains obscure. CSN subunits have been implicated in various cellular processes, suggesting a possible role for the CSN as an integrator of multiple signaling pathways. In order to elucidate the function of the CSN in animals, a Drosophila model system has previously been established. Gel-filtration analysis with antibodies against CSN subunits 4, 5 and 7 revealed that these proteins act as a complex in Drosophila that is similar in size to the plant and mammalian complexes. Null mutations in either one of two subunits, CSN4 or CSN5, are larval lethal. Successful embryogenesis appears to be a consequence of maternal contribution of the complex. Biochemical analysis indicates that the different subunits are found in both CSN-dependent and CSN-independent forms, and that these forms are differentially affected by the mutations. Phenotypic characterization of these two mutants indicates that they show both shared and unique phenotypes, which suggest specific roles for each subunit. Both mutants have defective oocyte and embryo patterning, and defects in response to DNA damage, while csn5 mutants develop melanotic tumors and csn4 mutants have phenotypes reminiscent of defects in ecdysone signaling.

Related Organizations
Keywords

COP9 Signalosome Complex, Cell Polarity, Proteins, Methyl Methanesulfonate, Repressor Proteins, Drosophila melanogaster, Oogenesis, Phenotype, Mutagenesis, Larva, Multiprotein Complexes, Oocytes, Animals, Drosophila Proteins, Body Patterning, Peptide Hydrolases, Signal Transduction

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Powered by OpenAIRE graph
citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
119
Top 10%
Top 10%
Top 10%