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Affinity proteomics reveals extensive phosphorylation of the Brassica chromosome axis protein ASY1 and a network of associated proteins at prophase I of meiosis.
Osman, Kim; Yang, Jianhua; Roitinger, Elisabeth; Lambing, Christophe; Heckmann, Stefan; Howell, Elaine; Cuacos, Maria; Imre, Richard; Dürnberger, Gerhard; Mechtler, Karl; Armstrong, Susan; Franklin, F Christopher H.
Afiliación
  • Osman K; School of Biosciences, University of Birmingham, Edgbaston, Birmingham, B15 2TT, UK.
  • Yang J; School of Biosciences, University of Birmingham, Edgbaston, Birmingham, B15 2TT, UK.
  • Roitinger E; IMP-IMBA, 1030, Vienna, Austria.
  • Lambing C; School of Biosciences, University of Birmingham, Edgbaston, Birmingham, B15 2TT, UK.
  • Heckmann S; School of Biosciences, University of Birmingham, Edgbaston, Birmingham, B15 2TT, UK.
  • Howell E; School of Biosciences, University of Birmingham, Edgbaston, Birmingham, B15 2TT, UK.
  • Cuacos M; School of Biosciences, University of Birmingham, Edgbaston, Birmingham, B15 2TT, UK.
  • Imre R; IMP-IMBA, 1030, Vienna, Austria.
  • Dürnberger G; IMP-IMBA, 1030, Vienna, Austria.
  • Mechtler K; Gregor Mendel Institute of Molecular Plant Biology, Dr. Bohr-Gasse 3, 1030, Vienna, Austria.
  • Armstrong S; IMP-IMBA, 1030, Vienna, Austria.
  • Franklin FCH; School of Biosciences, University of Birmingham, Edgbaston, Birmingham, B15 2TT, UK.
Plant J ; 93(1): 17-33, 2018 Jan.
Article en En | MEDLINE | ID: mdl-29078019
ABSTRACT
During meiosis, the formation of crossovers (COs) generates genetic variation and provides physical links that are essential for accurate chromosome segregation. COs occur in the context of a proteinaceous chromosome axis. The transcriptomes and proteomes of anthers and meiocytes comprise several thousand genes and proteins, but because of the level of complexity relatively few have been functionally characterized. Our understanding of the physical and functional interactions between meiotic proteins is also limited. Here we use affinity proteomics to analyse the proteins that are associated with the meiotic chromosome axis protein, ASY1, in Brassica oleracea anthers and meiocytes. We show that during prophase I ASY1 and its interacting partner, ASY3, are extensively phosphorylated, and we precisely assign phosphorylation sites. We identify 589 proteins that co-immunoprecipitate with ASY1. These correspond to 492 Arabidopsis orthologues, over 90% of which form a coherent protein-protein interaction (PPI) network containing known and candidate meiotic proteins, including proteins more usually associated with other cellular processes such as DNA replication and proteolysis. Mutant analysis confirms that affinity proteomics is a viable strategy for revealing previously unknown meiotic proteins, and we show how the PPI network can be used to prioritise candidates for analysis. Finally, we identify another axis-associated protein with a role in meiotic recombination. Data are available via ProteomeXchange with identifier PXD006042.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proteínas de Plantas / Brassica / Segregación Cromosómica / Proteoma / Proteómica Tipo de estudio: Risk_factors_studies Idioma: En Revista: Plant J Asunto de la revista: BIOLOGIA MOLECULAR / BOTANICA Año: 2018 Tipo del documento: Article País de afiliación: Reino Unido

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Proteínas de Plantas / Brassica / Segregación Cromosómica / Proteoma / Proteómica Tipo de estudio: Risk_factors_studies Idioma: En Revista: Plant J Asunto de la revista: BIOLOGIA MOLECULAR / BOTANICA Año: 2018 Tipo del documento: Article País de afiliación: Reino Unido