<i>Trichoderma reesei</i> Rad51 tolerates mismatches in hybrid meiosis with diverse genome sequences.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 33593897.
- Also identified by DOI 10.1073/pnas.2007192118 and PMC identifier 7923544.
- Licence recorded as CC BY-NC-ND.
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Abstract
Most eukaryotes possess two RecA-like recombinases (ubiquitous Rad51 and meiosis-specific Dmc1) to promote interhomolog recombination during meiosis. However, some eukaryotes have lost Dmc1. Given that mammalian and yeast <i>Saccharomyces cerevisiae</i> (<i>Sc</i>) Dmc1 have been shown to stabilize recombination intermediates containing mismatches better than Rad51, we used the Pezizomycotina filamentous fungus <i>Trichoderma reesei</i> to address if and how Rad51-only eukaryotes conduct interhomolog recombination in zygotes with high sequence heterogeneity. We applied multidisciplinary approaches (next- and third-generation sequencing technology, genetics, cytology, bioinformatics, biochemistry, and single-molecule biophysics) to show that <i>T. reesei</i> Rad51 (<i>Tr</i>Rad51) is indispensable for interhomolog recombination during meiosis and, like <i>Sc</i>Dmc1, <i>Tr</i>Rad51 possesses better mismatch tolerance than <i>Sc</i>Rad51 during homologous recombination. Our results also indicate that the ancestral <i>Tr</i>Rad51 evolved to acquire <i>Sc</i>Dmc1-like properties by creating multiple structural variations, including via amino acid residues in the L1 and L2 DNA-binding loops.
Medical subject headings
- Cell Cycle Proteins
- DNA-Binding Proteins
- Fungal Proteins
- Genome, Fungal
- Homologous Recombination
- Hypocreales
- Meiosis
- Rad51 Recombinase
- Saccharomyces cerevisiae Proteins