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Identification of novel synaptonemal complex components in C. elegans.
Hurlock, Matthew E; Cavka, Ivana; Kursel, Lisa E; Haversat, Jocelyn; Wooten, Matthew; Nizami, Zehra; Turniansky, Rashi; Hoess, Philipp; Ries, Jonas; Gall, Joseph G; Rog, Ofer; Köhler, Simone; Kim, Yumi.
Afiliação
  • Hurlock ME; Department of Biology, Johns Hopkins University, Baltimore, MD.
  • Cavka I; The European Molecular Biology Laboratory, Heidelberg, Germany.
  • Kursel LE; School of Biological Sciences, University of Utah, Salt Lake City, UT.
  • Haversat J; Department of Biology, Johns Hopkins University, Baltimore, MD.
  • Wooten M; Department of Biology, Johns Hopkins University, Baltimore, MD.
  • Nizami Z; Department of Embryology, Carnegie Institution for Science, Baltimore, MD.
  • Turniansky R; Department of Biology, Johns Hopkins University, Baltimore, MD.
  • Hoess P; The European Molecular Biology Laboratory, Heidelberg, Germany.
  • Ries J; Collaboration for joint PhD degree between European Molecular Biology Laboratory and Faculty of Biosciences, Heidelberg University, Heidelberg, Germany.
  • Gall JG; The European Molecular Biology Laboratory, Heidelberg, Germany.
  • Rog O; Department of Embryology, Carnegie Institution for Science, Baltimore, MD.
  • Köhler S; School of Biological Sciences, University of Utah, Salt Lake City, UT.
  • Kim Y; The European Molecular Biology Laboratory, Heidelberg, Germany.
J Cell Biol ; 219(5)2020 05 04.
Article em En | MEDLINE | ID: mdl-32211899
ABSTRACT
The synaptonemal complex (SC) is a tripartite protein scaffold that forms between homologous chromosomes during meiosis. Although the SC is essential for stable homologue pairing and crossover recombination in diverse eukaryotes, it is unknown how individual components assemble into the highly conserved SC structure. Here we report the biochemical identification of two new SC components, SYP-5 and SYP-6, in Caenorhabditis elegans. SYP-5 and SYP-6 are paralogous to each other and play redundant roles in synapsis, providing an explanation for why these genes have evaded previous genetic screens. Superresolution microscopy reveals that they localize between the chromosome axes and span the width of the SC in a head-to-head manner, similar to the orientation of other known transverse filament proteins. Using genetic redundancy and structure-function analyses to truncate C-terminal tails of SYP-5/6, we provide evidence supporting the role of SC in both limiting and promoting crossover formation.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Recombinação Genética / Complexo Sinaptonêmico / Proteínas Cromossômicas não Histona / Caenorhabditis elegans Tipo de estudo: Diagnostic_studies Limite: Animals Idioma: En Revista: J Cell Biol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Moldávia

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Recombinação Genética / Complexo Sinaptonêmico / Proteínas Cromossômicas não Histona / Caenorhabditis elegans Tipo de estudo: Diagnostic_studies Limite: Animals Idioma: En Revista: J Cell Biol Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Moldávia