2023
DOI: 10.1016/j.cj.2022.07.022
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Fertility, genome stability, and homozygosity in a diverse set of resynthesized rapeseed lines

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Cited by 6 publications
(4 citation statements)
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“…In support of our results, non-homologous translocations between the A and C genomes have previously been observed in B. napus using various methods, including microscopy (Osborn et al 2003;Sheidai et al 2003) segregation distortion of mapping populations (Schranz and Osborn 2000;Stein et al 2017) , and sequence read mapping depth (Chalhoub et al 2014;Samans et al 2017). Non-homologous pairing in polyploids has also been observed in several other polyploid species, although the frequency is rather low compared to synthetic polyploids (Madlung et al 2005;Henry et al 2014;Ihnien Katche et al 2022) and, even though different chromosomes might interact during the initial stages of meiosis, these configurations tend to resolve into correct homolog pairing (bivalent formation) as meiosis progresses (Comai et al 2003). How meiotic stabilization or diploid-like behavior has been achieved in natural polyploids is not yet fully understood, although many potential hypothesis have been described, involving for example new mutations, changes in genetic regulation, or inheritance of pre-adapted alleles (reviewed in (Gonzalo 2022)).…”
Section: Discussionsupporting
confidence: 90%
“…In support of our results, non-homologous translocations between the A and C genomes have previously been observed in B. napus using various methods, including microscopy (Osborn et al 2003;Sheidai et al 2003) segregation distortion of mapping populations (Schranz and Osborn 2000;Stein et al 2017) , and sequence read mapping depth (Chalhoub et al 2014;Samans et al 2017). Non-homologous pairing in polyploids has also been observed in several other polyploid species, although the frequency is rather low compared to synthetic polyploids (Madlung et al 2005;Henry et al 2014;Ihnien Katche et al 2022) and, even though different chromosomes might interact during the initial stages of meiosis, these configurations tend to resolve into correct homolog pairing (bivalent formation) as meiosis progresses (Comai et al 2003). How meiotic stabilization or diploid-like behavior has been achieved in natural polyploids is not yet fully understood, although many potential hypothesis have been described, involving for example new mutations, changes in genetic regulation, or inheritance of pre-adapted alleles (reviewed in (Gonzalo 2022)).…”
Section: Discussionsupporting
confidence: 90%
“…Resynthesized lines serve as valuable genetic resources in rapeseed breeding, contributing genetic diversity and crucial traits such as disease resistance (clubroot disease, sclerotinia stem rot, verticillium wilt, blackleg disease), yield, heterosis, insect resistance, pod shatter resistance, early flowering, and drought tolerance 42 . While some artificial rapeseeds were initially used solely as breeding materials due to low yields 36 , 43 , 44 , improved pollen and seed fertility have been achieved in advanced generations 41 , 45 , 46 . Consequently, selection lines from advanced generations with enhanced self-compatibility and seed fertility can be directly utilized for varietal development.…”
Section: Discussionmentioning
confidence: 99%
“…To achieve this goal in inbred B. napus, it will be necessary to look to related species (Katche et al 2019). Brassica napus germplasm can be readily enriched by using resynthesis: genotypes of progenitor species B. rapa × B. oleracea can be utilized to directly produce 2n = AACC types, which are optimal for further breeding (Katche et al 2023). Direct crossing between B. rapa and B. napus can also be carried out, followed by selection for euploid (2n = AACC) progeny; likewise crosses between B. oleracea and B. napus, although these often require embryo rescue (reviewed by FitzJohn et al 2007).…”
Section: A Critical Discussion Of the Pyramiding Strategymentioning
confidence: 99%