2008
DOI: 10.1016/j.jas.2007.03.003
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Molecular markers for the discrimination of Triticum turgidum L. subsp. dicoccum (Schrank ex Schübl.) Thell. and Triticum timopheevii (Zhuk.) Zhuk. subsp. timopheevii

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Cited by 14 publications
(9 citation statements)
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“…Their prevalence in the archaeobotanical record in combination with them often being morphologically well-preserved has made them into attractive targets for genetic analyses. Genetic analyses of such materials have, however, produced mixed results (Boscato, et al, 2008;Bunning, et al, 2012;Oliveira, et al, 2012b;Bilgic, et al, 2016;Castillo, et al, 2016). Nistelberger, et al, (2016) evaluated charred materials of barley, grape, maize and rice using whole-genome sequencing with and without capture, which showed that the chances of successful analysis are exceptionally low and hardly worthwhile.…”
Section: Resultsmentioning
confidence: 99%
“…Their prevalence in the archaeobotanical record in combination with them often being morphologically well-preserved has made them into attractive targets for genetic analyses. Genetic analyses of such materials have, however, produced mixed results (Boscato, et al, 2008;Bunning, et al, 2012;Oliveira, et al, 2012b;Bilgic, et al, 2016;Castillo, et al, 2016). Nistelberger, et al, (2016) evaluated charred materials of barley, grape, maize and rice using whole-genome sequencing with and without capture, which showed that the chances of successful analysis are exceptionally low and hardly worthwhile.…”
Section: Resultsmentioning
confidence: 99%
“…timopheevii , a marker must also give a null or diagnostic signal for the A genome, which diverged from the ancestor of the B and G genomes approximately 7 million years ago [9,10] and so also has extensive sequence similarity. Early studies indicated that the multicopy ribosomal DNA (rDNA) transcription units have features that enable the three genomes to be distinguished [11,12], and two polymerase chain reactions (PCRs) intended to be specific for the internal transcribed spacer of the G genome rDNA units were designed for identification of archaeological specimens [13]. However, one of these PCRs gave nonspecific amplification products with modern T .…”
Section: Introductionmentioning
confidence: 99%
“…Boscato et al (2008), in their quest to identify T. timopheevii from charred fossil remains, designed ribosomal internal transcribed spacer primers discriminating T. timopheevii and T. dicoccum but were unsuccessful in retrieving ancient DNA. We also applied this approach to modern timopheevii, but in vain.…”
Section: Introductionmentioning
confidence: 99%