1994
DOI: 10.2307/2419718
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matK DNA Sequences and Phylogenetic Reconstruction in Saxifragaceae s. str.

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Cited by 486 publications
(265 citation statements)
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“…Double-stranded DNAs were amplified by using PCR to amplify the ITS-1, ITS-2, and 5.8S region of nuclear ribosomal DNA using the ITS-4 and ITS-5 primers (23). The cpDNA trnK introns and matK coding region were amplified by using the primers trnK-3914F and trnK-2R (24). PCR products were cloned into plasmids by using a TOPO TA cloning kit (Invitrogen).…”
Section: Methodsmentioning
confidence: 99%
“…Double-stranded DNAs were amplified by using PCR to amplify the ITS-1, ITS-2, and 5.8S region of nuclear ribosomal DNA using the ITS-4 and ITS-5 primers (23). The cpDNA trnK introns and matK coding region were amplified by using the primers trnK-3914F and trnK-2R (24). PCR products were cloned into plasmids by using a TOPO TA cloning kit (Invitrogen).…”
Section: Methodsmentioning
confidence: 99%
“…These included portions of three low-copy nuclear genes: chloroplast-expressed glutamine synthetase (ncpGS), nitrate reductase (NIA), and the fourth intron of phosphoenolpyruvate carboxylase (PepC) and eight noncoding regions of the chloroplast genome, selected for their relatively high variability in other angiosperms: six intergenic regions (petN-psbM, psbE-petL, psbM-trnD, trnD-trnT, and trnQ-rpS16); a portion of the tRNA-Lys (trnK) intron with primers in 5 0 trnK and 5 0 matK; a portion of the trnK intron with primers in 3 0 matK and 3 0 trnK; and the RPS16 intron. PCR primers were previously published (Demesure et al, 1995;Emshwiller and Doyle, 1999;Gaskin and Schaal, 2002;Howarth and Baum, 2002;Johnson and Soltis, 1994;Lee and Wen, 2004;Popp et al, 2005;Popp and Oxelman, 2001;Shaw et al, 2005Shaw et al, , 2007 or designed for this study (Supplementary Table S1). …”
Section: Dna Isolation Amplification and Sequencingmentioning
confidence: 99%
“…Generally, DNA extraction procedures were from silica-gel-dried leaves (Chase and Hills 1991) or herbarium sheets as summarized by Fay et al (2000). A description of the amplification procedures for the seven loci can be found in the following references: rbcL , atpB , trnL-F (primers "c" and "f" of Taber let et al 1991, which include two regions, trnL intron and trnL-F intergenic spacer), matK (Johnson and Soltis 1994), ndhF (Pires and Sytsma 2002;McPherson et al submitted), and atp 1 (Davis et al 1998Stevenson et al 2000). GenBank numbers for rbcL, atpB, and trnL-F have been previously published Pireset al 2004).…”
Section: Dna Extraction Gene Amplification Sequencing and Alignmentmentioning
confidence: 99%