Analysis of the processing of complex recombination intermediates by structure-selective endonucleases

  1. Raquel Carreira Rodríguez
Supervised by:
  1. Miguel González Blanco Director

Defence university: Universidade de Santiago de Compostela

Fecha de defensa: 10 March 2023

Committee:
  1. Dana Branzei Chair
  2. Anxo Vidal Figueroa Secretary
  3. Aura Carreira Moreno Committee member
Department:
  1. Department of Biochemistry and Molecular Biology

Type: Thesis

Abstract

DNA repair by homologous recombination involves the formation of branched intermediates that can constitute a source of genome instability when untimely processed. To prevent these structures from interfering with chromosome segregation, cells rely on the action of the structure-selective endonucleases Mus81-Mms4 and Yen1. Here, we employed a biochemical approach to show that both endonucleases can process the central intermediate of this pathway, the displacement loop (D-loop). Using synthetic and enzymatically reconstituted D-loops, we mapped their incision sites and recapitulated for the first time the formation of a half-crossover precursor in vitro. This implies that the concurrent action of Mus81-Mms4 and Yen1 on a D-loop may lead to the generation of complex chromosomal rearrangements.