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The molecular machinery of meiotic recombination.
Chen, Linda; Weir, John R.
Affiliation
  • Chen L; Structural Biochemistry of Meiosis Group, Friedrich Miescher Laboratory, Max-Planck-Ring 9, 72076 Tübingen, Germany.
  • Weir JR; Structural Biochemistry of Meiosis Group, Friedrich Miescher Laboratory, Max-Planck-Ring 9, 72076 Tübingen, Germany.
Biochem Soc Trans ; 52(1): 379-393, 2024 Feb 28.
Article in En | MEDLINE | ID: mdl-38348856
ABSTRACT
Meiotic recombination, a cornerstone of eukaryotic diversity and individual genetic identity, is essential for the creation of physical linkages between homologous chromosomes, facilitating their faithful segregation during meiosis I. This process requires that germ cells generate controlled DNA lesions within their own genome that are subsequently repaired in a specialised manner. Repair of these DNA breaks involves the modulation of existing homologous recombination repair pathways to generate crossovers between homologous chromosomes. Decades of genetic and cytological studies have identified a multitude of factors that are involved in meiotic recombination. Recent work has started to provide additional mechanistic insights into how these factors interact with one another, with DNA, and provide the molecular outcomes required for a successful meiosis. Here, we provide a review of the recent developments with a focus on protein structures and protein-protein interactions.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA Breaks, Double-Stranded / Homologous Recombination Type of study: Prognostic_studies Language: En Journal: Biochem Soc Trans Year: 2024 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: DNA Breaks, Double-Stranded / Homologous Recombination Type of study: Prognostic_studies Language: En Journal: Biochem Soc Trans Year: 2024 Document type: Article Affiliation country: