2020
DOI: 10.3389/fpls.2020.00710
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Analysis of Structural Genomic Diversity in Aegilops umbellulata, Ae. markgrafii, Ae. comosa, and Ae. uniaristata by Fluorescence In Situ Hybridization Karyotyping

Abstract: Fluorescence in situ hybridization karyotypes have been widely used for evolutionary analysis on chromosome organization and genetic/genomic diversity in the wheat alliance (tribe Triticeae of Poaceae). The karyotpic diversity of Aegilops umbellulata, Ae. markgrafii, Ae. comosa subsp. comosa and subsp. subventricosa, and Ae. uniaristata was evaluated by the fluorescence in situ hybridization (FISH) probes oligo-pSc119.2 and pTa71 in combination with (AAC) 5 , (ACT) 7 , and (CTT) 12 , respectively. Abundant int… Show more

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Cited by 21 publications
(24 citation statements)
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References 80 publications
(119 reference statements)
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“…Four oligonucleotide probes, namely Oligo-pSc119.2-1 (pSc119.2), Oligo-pTa535-1 (pTa-535), Oligo-pTa71-2 (pTa71) (Tang et al 2014), and (CTT) 12 (Song et al 2020), were used for FISH analysis. These probes were synthesized by Tsingke in Chengdu, China.…”
Section: Cytological Observation and Fish Analysismentioning
confidence: 99%
See 1 more Smart Citation
“…Four oligonucleotide probes, namely Oligo-pSc119.2-1 (pSc119.2), Oligo-pTa535-1 (pTa-535), Oligo-pTa71-2 (pTa71) (Tang et al 2014), and (CTT) 12 (Song et al 2020), were used for FISH analysis. These probes were synthesized by Tsingke in Chengdu, China.…”
Section: Cytological Observation and Fish Analysismentioning
confidence: 99%
“…The polymorphism of FISH signals among 48 Ae. comosa accessions were discovered using probes pSc119.2, (CTT) 12 and pTa 71, which allowed precise identi cation of M chromosomes from different accessions (Song et al 2020). Single nucleotide polymorphisms (SNPs) are one of the most abundant molecular markers in plant (Lai et al 2012;Cui et al 2017).…”
Section: Introductionmentioning
confidence: 99%
“…Fluorescent in situ hybridization (FISH) is a powerful molecular cytogenetic technique to characterize karyotype variation at chromosome level by direct localization of repetitive DNA sequences on plant chromosomes ( Jiang and Gill, 2006 ; Patokar et al, 2016 ; Song et al, 2020 ), enabling identification of chromosomes even in species with small and morphologically indistinguishable chromosomes, and comparison of chromosomal organization between species. However, such probes can be inconsistent in chromosome identification for multiplicity of repeat sequences and variations in their genomic locations ( Mukai et al, 1993 ; Fransz et al, 1998 ; Kato et al, 2004 ; Danilova et al, 2012 ; Komuro et al, 2013 ; Koo et al, 2016 ; Amosova et al, 2017 ; Krivankova et al, 2017 ; Hou et al, 2018 ; Said et al, 2018 ), and repetitive DNA sequences with suitable genomic locations may not exist.…”
Section: Introductionmentioning
confidence: 99%
“…Up to now, several wheat-Ae. biuncialis disomic addition lines have been developed carrying the chromosomes 1U, 3U, 6U, 2M, 3M, 5M and 7M besides the whole wheat genome, respectively [30][31][32] . In addition, a 3M.4BS translocation line possessing the 3M chromosome arm from Ae.…”
mentioning
confidence: 99%