2016
DOI: 10.3897/compcytogen.v10i4.9666
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Chromosomal organization of repetitive DNAs in Hordeum bogdanii and H. brevisubulatum (Poaceae)

Abstract: Molecular karyotypes of Hordeum bogdanii Wilensky, 1918 (2n = 14), and Hordeum brevisubulatum Link, 1844 ssp. brevisubulatum (2n = 28), were characterized by physical mapping of several repetitive sequences. A total of 18 repeats, including all possible di- or trinucleotide SSR (simple sequence repeat) motifs and satellite DNAs, such as pAs1, 5S rDNA, 45S rDNA, and pSc119.2, were used as probes for fluorescence in situ hybridization on root-tip metaphase chromosomes. Except for the SSR motifs AG, AT and GC, al… Show more

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Cited by 15 publications
(22 citation statements)
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“…In this study, all potential dinucleotide and trinucleotide SSRs and four satellite DNA repeats were used to characterize the P genome of five Agropyron species. Unlike other genomes such as the H, I, A, B, and D genomes in Triticeae (Cuadrado et al 2007; 2008 ; Dou et al 2016 ), which include a number of SSR hybridization signals based on FISH , the P genome in Agropyron harbored only the dinucleotide SSRs AG and AC in all species, except A. mongolicum , and fewer trinucleotide SSRs in the different species.…”
Section: Discussionmentioning
confidence: 86%
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“…In this study, all potential dinucleotide and trinucleotide SSRs and four satellite DNA repeats were used to characterize the P genome of five Agropyron species. Unlike other genomes such as the H, I, A, B, and D genomes in Triticeae (Cuadrado et al 2007; 2008 ; Dou et al 2016 ), which include a number of SSR hybridization signals based on FISH , the P genome in Agropyron harbored only the dinucleotide SSRs AG and AC in all species, except A. mongolicum , and fewer trinucleotide SSRs in the different species.…”
Section: Discussionmentioning
confidence: 86%
“…All potential dinucleotide and trinucleotide SSRs and four satellite DNA sequences, namely pAs1 ( Rayburn and Gill 1986 ), pSc119.2 ( Bedbrook et al 1980 ), 5S and 45S rDNA, were used to generate DNA probes. The procedure for labeling the above sequences was performed in accordance with the method of Dou et al (2016) .…”
Section: Methodsmentioning
confidence: 99%
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