SCF-Fbxo42 promotes synaptonemal complex assembly by downregulating PP2A-B56 |
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| Authors: | Pedro Barbosa Liudmila Zhaunova Simona Debilio Verdiana Steccanella Van Kelly Tony Ly Hiroyuki Ohkura |
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| Affiliation: | 1.Wellcome Centre for Cell Biology, School of Biological Sciences, University of Edinburgh, Edinburgh, UK;2.Department of Biology and Biotechnology, University of Pavia, Pavia, Italy |
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| Abstract: | Meiosis creates genetic diversity by recombination and segregation of chromosomes. The synaptonemal complex assembles during meiotic prophase I and assists faithful exchanges between homologous chromosomes, but how its assembly/disassembly is regulated remains to be understood. Here, we report how two major posttranslational modifications, phosphorylation and ubiquitination, cooperate to promote synaptonemal complex assembly. We found that the ubiquitin ligase complex SCF is important for assembly and maintenance of the synaptonemal complex in Drosophila female meiosis. This function of SCF is mediated by two substrate-recognizing F-box proteins, Slmb/βTrcp and Fbxo42. SCF-Fbxo42 down-regulates the phosphatase subunit PP2A-B56, which is important for synaptonemal complex assembly and maintenance. |
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