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Status: Bibliographieeintrag

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Verfasst von:Sato-Carlton, Aya [VerfasserIn]   i
 Nakamura-Tabuchi, Chihiro [VerfasserIn]   i
 Li, Xuan [VerfasserIn]   i
 Boog, Hendrik [VerfasserIn]   i
 Lehmer, Madison K. [VerfasserIn]   i
 Rosenberg, Scott C. [VerfasserIn]   i
 Barroso, Consuelo [VerfasserIn]   i
 Martinez-Perez, Enrique [VerfasserIn]   i
 Corbett, Kevin D. [VerfasserIn]   i
 Carlton, Peter Mark [VerfasserIn]   i
Titel:Phosphoregulation of HORMA domain protein HIM-3 promotes asymmetric synaptonemal complex disassembly in meiotic prophase in Caenorhabditis elegans
Verf.angabe:Aya Sato-Carlton, Chihiro Nakamura-Tabuchi, Xuan Li, Hendrik Boog, Madison K. Lehmer, Scott C. Rosenberg, Consuelo Barroso, Enrique Martinez-Perez, Kevin D. Corbett, Peter Mark Carlton
E-Jahr:2020
Jahr:November 11, 2020
Fussnoten:Gesehen am 05.02.2021
Titel Quelle:Enthalten in: Public Library of SciencePLoS Genetics
Ort Quelle:San Francisco, Calif. : Public Library of Science, 2005
Jahr Quelle:2020
Band/Heft Quelle:16(2020,11) Artikel-Nummer e1008968, 33 Seiten
ISSN Quelle:1553-7404
Abstract:In the two cell divisions of meiosis, diploid genomes are reduced into complementary haploid sets through the discrete, two-step removal of chromosome cohesion, a task carried out in most eukaryotes by protecting cohesion at the centromere until the second division. In eukaryotes without defined centromeres, however, alternative strategies have been innovated. The best-understood of these is found in the nematode Caenorhabditis elegans: after the single off-center crossover divides the chromosome into two segments, or arms, several chromosome-associated proteins or post-translational modifications become specifically partitioned to either the shorter or longer arm, where they promote the correct timing of cohesion loss through as-yet unknown mechanisms. Here, we investigate the meiotic axis HORMA-domain protein HIM-3 and show that it becomes phosphorylated at its C-terminus, within the conserved “closure motif” region bound by the related HORMA-domain proteins HTP-1 and HTP-2. Binding of HTP-2 is abrogated by phosphorylation of the closure motif in in vitro assays, strongly suggesting that in vivo phosphorylation of HIM-3 likely modulates the hierarchical structure of the chromosome axis. Phosphorylation of HIM-3 only occurs on synapsed chromosomes, and similarly to other previously-described phosphorylated proteins of the synaptonemal complex, becomes restricted to the short arm after designation of crossover sites. Regulation of HIM-3 phosphorylation status is required for timely disassembly of synaptonemal complex central elements from the long arm, and is also required for proper timing of HTP-1 and HTP-2 dissociation from the short arm. Phosphorylation of HIM-3 thus plays a role in establishing the identity of short and long arms, thereby contributing to the robustness of the two-step chromosome segregation.
DOI:doi:10.1371/journal.pgen.1008968
URL:Bitte beachten Sie: Dies ist ein Bibliographieeintrag. Ein Volltextzugriff für Mitglieder der Universität besteht hier nur, falls für die entsprechende Zeitschrift/den entsprechenden Sammelband ein Abonnement besteht oder es sich um einen OpenAccess-Titel handelt.

Volltext ; Verlag: https://doi.org/10.1371/journal.pgen.1008968
 Volltext: https://journals.plos.org/plosgenetics/article?id=10.1371/journal.pgen.1008968
 DOI: https://doi.org/10.1371/journal.pgen.1008968
Datenträger:Online-Ressource
Sprache:eng
Sach-SW:Caenorhabditis elegans
 Chromosome staining
 Gonads
 Immunostaining
 Meiosis
 Oocytes
 Phosphorylation
 Synapsis
K10plus-PPN:1747632422
Verknüpfungen:→ Zeitschrift

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