1994
DOI: 10.1007/bf00226978
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Phylogenetic analysis of Sorghum and related taxa using internal transcribed spacers of nuclear ribosomal DNA

Abstract: The phylogenetic relationships of the genus Sorghum and related genera were studied by sequencing the nuclear ribosomal DNA (rDNA) internal transcribed spacer region (ITS). DNA was extracted from 15 Sorghum accessions, including one accession from each of the sections Chaetosorghum and Heterosorghum, four accessions from Parasorghum, two accessions from Stiposorghum, and seven representatives from three species of the section Sorghum (one accession from each of S. propinquum and S. halepense, and five races of… Show more

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Cited by 717 publications
(374 citation statements)
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“…The ITS region consisted of the 3' and 5' ends of the 18S and 26S ribosomal RNA genes, respectively, the internal transcribed spacers (ITS1 and ITS2), and the intervening 5.8S gene of the nuclear ribosomal multigene family. Amplifications of this region were performed using primers 17SE and 26SE (Sun et al 1994). We used an internal fragment of approximately 630 bp of the matK gene, amplified with primers matK-F2 and matK-R2 (Batista et al 2013), which approximately corresponds to the region widely used for barcoding land plants (Chase et al 2007).…”
Section: Methodsmentioning
confidence: 99%
“…The ITS region consisted of the 3' and 5' ends of the 18S and 26S ribosomal RNA genes, respectively, the internal transcribed spacers (ITS1 and ITS2), and the intervening 5.8S gene of the nuclear ribosomal multigene family. Amplifications of this region were performed using primers 17SE and 26SE (Sun et al 1994). We used an internal fragment of approximately 630 bp of the matK gene, amplified with primers matK-F2 and matK-R2 (Batista et al 2013), which approximately corresponds to the region widely used for barcoding land plants (Chase et al 2007).…”
Section: Methodsmentioning
confidence: 99%
“…(b) PCR amplification and DNA sequencing A total of 1230 aligned nucleotide positions across the ITS and ETS (Baldwin et al 1995;Baldwin & Markos 1998) were amplified using primers 17SE and 26SE (Sun et al 1994) and Hel1 and 18S ETS (Baldwin & Markos 1998), respectively. Standard automated sequencing protocols ( Jousselin et al 2003) were used except that DMSO was added to all reactions.…”
Section: Methodsmentioning
confidence: 99%
“…For the trnL intron amplification we used the two universal primers C (forward) and D (reverse) (Taberlet et al, 1991), and PCR conditions consisting of 3 min denaturing step at 94°C, 40 cycles of 1 min at 94°C (denaturation), 30 s at 50°C (annealing), 1 min at 72°C (extension), and further extension for 10 min at 72°C. For the nuclear ribosomal ITS/5.8S region we used the amplification primers 17SE and 26SE (Sun et al, 1994) and the sequencing primers ITS 92 (Desfeux and Lejeune, 1996) and ITS 04 (White et al, 1990). The ITS/5.8S region was amplified using a run program with a 3 min denaturing step at 94°C, followed by 28-30 cycles of 1 min at 94°C (denaturation); 1 min at 50-52°C (annealing); 2:30 min at 72°C (extension) and further extension for 7 min at 72°C.…”
Section: Dna Amplification and Sequencingmentioning
confidence: 99%