Abstract

SCCRO (squamous cell carcinoma-related oncogene; also known as DCUN1D1) is a highly conserved gene that functions as an E3 in neddylation. Although inactivation of SCCRO in yeast results in lethality, SCCRO(-/-) mice are viable. The exclusive presence of highly conserved paralogues in higher organisms led us to assess whether compensation by SCCRO paralogues rescues lethality in SCCRO(-/-) mice. Using murine and Drosophila models, we assessed the in vivo activities of SCCRO and its paralogues in cullin neddylation. We found that SCCRO family members have overlapping and antagonistic activity that regulates neddylation and cell proliferation activities in vivo. In flies, both dSCCRO and dSCCRO3 promote neddylation and cell proliferation, whereas dSCCRO4 negatively regulates these processes. Analysis of somatic clones showed that the effects that these paralogues have on proliferation serve to promote cell competition, leading to apoptosis in clones with a net decrease in neddylation activity. We found that dSCCRO and, to a lesser extent, dSCCRO3 rescue the neddylation and proliferation defects promoted by expression of SCCRO4. dSCCRO and dSCCRO3 functioned cooperatively, with their coexpression resulting in an increase in both the neddylated cullin fraction and proliferation activity. In contrast, human SCCRO and SCCRO4 promote, and human SCCRO3 inhibits, neddylation and proliferation when expressed in flies. Our findings provide the first insights into the mechanisms through which SCCRO family members cooperatively regulate neddylation and cell proliferation.

Highlights

  • The highly conserved tripartite enzymatic cascade that results in posttranslational modification by ubiquitin regulates the activity of proteins involved in diverse cellular processes [1,2,3]

  • Mammalian SCCRO Paralogues Promote Cullin Neddylation— Given that the SCCRO orthologue DCN1 is essential for development in yeast and C. elegans, it was somewhat unexpected that SCCROϪ/Ϫ mice were found to be viable, albeit with runting and male-specific infertility [19, 20]

  • Four of the five paralogues (SCCRO, SCCRO2, SCCRO4, and SCCRO5), which were found to bind to UBC12 [27], promoted neddylation of cullins in vitro (Fig. 1B)

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Summary

Introduction

The highly conserved tripartite enzymatic cascade that results in posttranslational modification by ubiquitin regulates the activity of proteins involved in diverse cellular processes [1,2,3]. To confirm and quantify the effects of SCCRO on cell proliferation, we used Ptc-Gal4 to express RNAi against dSCCRO in the middle wing patch between veins L3 and L4.

Results
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