“…While recombination in short repeats is rare and has yet to be associated with CMS (Touzet and Meyer, 2014), these repeats may have played other roles in evolution (Andre et al, 1992), leading to other deficiencies such as respiratory impairments (Kitazaki and Kubo, 2010). A final comment is that many nuclear genes, including Msh1 (Abdelnoor et al, 2003;Shedge et al, 2007;Galtier, 2011), RecA2 (Shedge et al, 2007), RecA1/4 (Odahara et al, 2009) and OSB1 (Zaegel et al, 2006), appear to participate in the regulation of recombination events for different repeated sequences (Lillestol et al, 2009;Cupp and Nielsen, 2014;Gualberto and Newton, 2017), which may represent an additional cytonuclear process important in the origin of CMS.…”