2022
DOI: 10.14348/molcells.2022.2054
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Fast and Precise: How to Measure Meiotic Crossovers in Arabidopsis

Abstract: During meiosis, homologous chromosomes (homologs) pair and undergo genetic recombination via assembly and disassembly of the synaptonemal complex. Meiotic recombination is initiated by excess formation of DNA double-strand breaks (DSBs), among which a subset are repaired by reciprocal genetic exchange, called crossovers (COs). COs generate genetic variations across generations, profoundly affecting genetic diversity and breeding. At least one CO between homologs is essential for the first meiotic chromosome se… Show more

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“…Since then, cytological methods, such as chromosome spreading, fluorescence in situ hybridization (FISH), and immunostaining, have been developed as classical and efficient approaches to interrogate meiosis and meiotic recombination in vivo (Armstrong, Sanchez‐Moran, & Franklin, 2009; Chelysheva et al., 2010; Wang, Cheng, Lu, Timofejeva, & Ma, 2014). Conventionally, CO interference quantification requires time‐consuming procedures, such as the generation of genome‐wide sets of pollen fluorescence‐tagged lines (FTLs) or construction of F 2 segregation populations (Kim & Choi, 2022) for monitoring meiotic recombination. By contrast, cytological assays have become convenient and effective approaches to analyze the number and distribution of COs and CO interference during meiosis (Armstrong, Caryl, Jones, & Franklin, 2002; Sanchez Moran, Armstrong, Santos, Franklin, & Jones, 2001).…”
Section: Introductionmentioning
confidence: 99%
“…Since then, cytological methods, such as chromosome spreading, fluorescence in situ hybridization (FISH), and immunostaining, have been developed as classical and efficient approaches to interrogate meiosis and meiotic recombination in vivo (Armstrong, Sanchez‐Moran, & Franklin, 2009; Chelysheva et al., 2010; Wang, Cheng, Lu, Timofejeva, & Ma, 2014). Conventionally, CO interference quantification requires time‐consuming procedures, such as the generation of genome‐wide sets of pollen fluorescence‐tagged lines (FTLs) or construction of F 2 segregation populations (Kim & Choi, 2022) for monitoring meiotic recombination. By contrast, cytological assays have become convenient and effective approaches to analyze the number and distribution of COs and CO interference during meiosis (Armstrong, Caryl, Jones, & Franklin, 2002; Sanchez Moran, Armstrong, Santos, Franklin, & Jones, 2001).…”
Section: Introductionmentioning
confidence: 99%