2000
DOI: 10.1002/1097-0320(20000901)41:1<36::aid-cyto5>3.0.co;2-o
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Use of fluorescence genomic in situ hybridization (GISH) to detect the presence of alien chromatin in wheat lines differing in nuclear DNA content

Abstract: Background Many times small differences in genome size are reported between or within plant species in which no cytologic confirmation is made. Attempts to repeat these studies have met with limited success. The controversy then becomes whether or not these small differences that were not confirmed cytologically are real. The present study was undertaken to determine if the ≈1% nuclear variation seen by flow cytometry among wheat lines selected for aluminum response was due to actual chromatin differences. Met… Show more

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Cited by 9 publications
(2 citation statements)
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“…This does not mean however, that all diploid varieties of a M. sacchariflorus have the identical nuclear DNA content. Intraspecific DNA content variation has been observed in various plant species (Rayburn et al 1989;Chung et al 1998;Wetzel and Rayburn 2000;(Rayburn et al 2004;Tatum et al 2006). Accessions of M. sacchariflorus, M. sinensis, or M. x giganteus could exist now or in the past that had a nuclear DNA content that would more precisely match the predicted nuclear DNA content of M. x giganteus.…”
Section: G1 Sorghummentioning
confidence: 99%
“…This does not mean however, that all diploid varieties of a M. sacchariflorus have the identical nuclear DNA content. Intraspecific DNA content variation has been observed in various plant species (Rayburn et al 1989;Chung et al 1998;Wetzel and Rayburn 2000;(Rayburn et al 2004;Tatum et al 2006). Accessions of M. sacchariflorus, M. sinensis, or M. x giganteus could exist now or in the past that had a nuclear DNA content that would more precisely match the predicted nuclear DNA content of M. x giganteus.…”
Section: G1 Sorghummentioning
confidence: 99%
“…For the GISH analysis, Mixed the P. huashanica genomic DNA and DiG-Nick Translation Mix (Roche, Germany) in a ratio of two to one at 15°C for 1.5 h as labeling probes following Wetzel et al [54] and Zhao et al [55]. The addition of Anti-Digoxigenin-Fluorescein mix (Roche, Germany) made the probes visualize after hybridization.…”
Section: In-situ Hybridizationmentioning
confidence: 99%