2021
DOI: 10.3390/agronomy11101988
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Identification of Parental Genome Construction and Inherited Morphological Characteristics in Triploid and AneuploidIntergeneric Hybrids from a Diploid−Diploid Cross between Citrus and Fortunella

Abstract: We previously obtained two intergeneric hybrids with different ploidies, i.e., aneuploid (2n = 28) and eutriploid, from diploid−diploid crosses between ‘Kiyomi’ tangor (Citrus unshiu Marcow. × C. sinensis (L.) Osbeck) and Meiwa kumquat (Fortunella crassifolia Swingle) as novel breeding materials for a seedless kumquat. In this study, we attempted to clarify the construction of the parental genomes of these hybrids by SSR genotyping and genomic in situ hybridization (GISH)−chromomycin A3 (CMA) analysis. SSR gen… Show more

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Cited by 2 publications
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“…This is an interesting case of competitive interactions found during the self-pollination of a diploid plant, and is likely the only example in the genus Citrus. This trait is very useful for agricultural production because unreduced gametes can be used for triploid citrus breeding (Aleza et al, 2010;Yasuda et al, 2021) and the competence of unreduced gamete production results in diploid self-compatible cultivars producing fruits with fewer seeds.…”
Section: Polyploidy and Self-incompatibility In Citrusmentioning
confidence: 99%
“…This is an interesting case of competitive interactions found during the self-pollination of a diploid plant, and is likely the only example in the genus Citrus. This trait is very useful for agricultural production because unreduced gametes can be used for triploid citrus breeding (Aleza et al, 2010;Yasuda et al, 2021) and the competence of unreduced gamete production results in diploid self-compatible cultivars producing fruits with fewer seeds.…”
Section: Polyploidy and Self-incompatibility In Citrusmentioning
confidence: 99%
“…6 SSR markers produced by Shimizu et al [21] were used in the present study (Table S1). PCR amplifications and electrophoresis of PCR-amplified products were carried out according to the methods described by Yasuda et al [22]. PCR amplifications were performed in a thermal controller (Biometra TAdvanced Thermocycler 96G, Analytik Jena, Jena, Germany) in a 5 µL final volume containing 0.5 ng µL −1 gDNA, 0.2 µM forward and reverse primers and 2.5 µL GoTaq Green Master Mix (Promega, Madison, WI, USA).…”
Section: Confirmation Of the Origin Of The Tetraploid Satsuma Mandarin By Ssr Analysismentioning
confidence: 99%