1997
DOI: 10.1007/bf00982535
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Phylogenetic analysis ofIridaceae with parsimony and distance methods using the plastid generps4

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Cited by 177 publications
(62 citation statements)
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“…The three most variable ones, ITS, trnG, and rps4 were selected for the investigation. ITS was amplified with the primers '18SF' and '26SR' (Rydin et al 2004), in a few cases with the internal primers '5.8F-Chrys' (Howis et al 2009) and '5.8SRPEny' (Nylinder et al 2013), trnG with the primers 'trnGf' and 'trnGr' (Pacak & Szweykowska-Kulińska 2000), and rps4 with 'rps5F' (Nadot et al 1994) and 'trnS' (Souza- Chies et al 1997). For all three markers the following PCR program was used: 5 min at 95°C followed by 4 cycles of 30 sec at 95°C, 30 sec at 57°C, 1 min at 72°C, 4 cycles of 30 sec at 95°C, 30 sec at 55°C, 1 min at 72°C and 34 cycles of 30 sec at 95°C, 30 sec at 57°C, 1 min at 72°C and a final elongation step of 8 min at 72°C.…”
Section: Molecular Methodsmentioning
confidence: 99%
“…The three most variable ones, ITS, trnG, and rps4 were selected for the investigation. ITS was amplified with the primers '18SF' and '26SR' (Rydin et al 2004), in a few cases with the internal primers '5.8F-Chrys' (Howis et al 2009) and '5.8SRPEny' (Nylinder et al 2013), trnG with the primers 'trnGf' and 'trnGr' (Pacak & Szweykowska-Kulińska 2000), and rps4 with 'rps5F' (Nadot et al 1994) and 'trnS' (Souza- Chies et al 1997). For all three markers the following PCR program was used: 5 min at 95°C followed by 4 cycles of 30 sec at 95°C, 30 sec at 57°C, 1 min at 72°C, 4 cycles of 30 sec at 95°C, 30 sec at 55°C, 1 min at 72°C and 34 cycles of 30 sec at 95°C, 30 sec at 57°C, 1 min at 72°C and a final elongation step of 8 min at 72°C.…”
Section: Molecular Methodsmentioning
confidence: 99%
“…Markers were amplified in 25 μL total volume including 50-150 ng genomic DNA, 1 × PCR buffer, 200 μM of each dNTP, 1 μM of each primer, and 0.65 U Ex Taq polymerase (TaKaRa Bio, Shiga, Japan). Previously published primers were used for trnL-F (Taberlet et al 1991; primers e and f), rbcL (Little and Barrington 2003), and rps4-trnS (Souza-Chies et al 1997;Li et al 2008). The PCR products were purified with ExoSAP-IT (USB Corp., Cleveland, Ohio) and sequenced in both directions using an ABI Prism 3130x1 automated sequencer (DNA Analysis Facility, Vermont Cancer Center, Burlington, Vermont) with the ABI Prism BigDye Terminator cycle sequence ready reaction kit (Applied Biosystems, Foster City, California).…”
Section: Methodsmentioning
confidence: 99%
“…Four chloroplast regions, including rpoC1 (Chase et al, 2007), rps4 (Nadot et al, 1994;Souza-Chies et al, 1997), trnG (Pacak and Szweykowska-Kulinska, 2000), and trnL-trnF (Taberlet et al, 1991) were selected for exhibiting the appropriate level of polymorphism at the species level in Bryoxiphium. These loci were amplified and sequenced following the protocols of Patiño et al (2015a).…”
Section: Taxon and Molecular Samplingmentioning
confidence: 99%