1994
DOI: 10.1093/sysbio/43.4.467
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Combining Data in Phylogenetic Systematics: An Empirical Approach Using Three Molecular Data Sets in the Solanaceae

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Cited by 553 publications
(140 citation statements)
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“…We used the following primers: ndhF5 (5′ ATGGAACATACATATCAATATTCATGG 3′) and ndhF2100 (5′CAAAGAAACTYGTAAKACSTACT CC 3′) (Olmstead & Sweere, 1994) to amplify ndhF; tabA (5′ CATTACAAATGCGATGCTCT 3′) and tabD (5′ GGGGATAGAGGGACTTGAAC 3′) (Taberlet & al., 1991) for trnT-L; ITS1 (5′ TCCGTAGGTGAACCTGCGG 3′), ITS2 (5′ GCTGCGTTCTTCATCGATGC 3′), ITS3 (5′ GCATCGATGAAGAACGCAGC 3′) and ITS4 (5′ TCCTCCGCTTATTGATATGC 3′) primers for the ITS1-5.8s-ITS2 region (White & al., 1990). PCR reactions were performed in a total volume of 50 µL, with the following composition: 5 μL 10× buffer containing MgCl 2 at 1.5 mmol/L (New England BioLabs), 0.1 mmol/L each dNTP, 0.2 µmol/L each primer and 0.02 U Taq DNA polymerase (New England Biolabs).…”
Section: Phylogenetic Analysismentioning
confidence: 99%
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“…We used the following primers: ndhF5 (5′ ATGGAACATACATATCAATATTCATGG 3′) and ndhF2100 (5′CAAAGAAACTYGTAAKACSTACT CC 3′) (Olmstead & Sweere, 1994) to amplify ndhF; tabA (5′ CATTACAAATGCGATGCTCT 3′) and tabD (5′ GGGGATAGAGGGACTTGAAC 3′) (Taberlet & al., 1991) for trnT-L; ITS1 (5′ TCCGTAGGTGAACCTGCGG 3′), ITS2 (5′ GCTGCGTTCTTCATCGATGC 3′), ITS3 (5′ GCATCGATGAAGAACGCAGC 3′) and ITS4 (5′ TCCTCCGCTTATTGATATGC 3′) primers for the ITS1-5.8s-ITS2 region (White & al., 1990). PCR reactions were performed in a total volume of 50 µL, with the following composition: 5 μL 10× buffer containing MgCl 2 at 1.5 mmol/L (New England BioLabs), 0.1 mmol/L each dNTP, 0.2 µmol/L each primer and 0.02 U Taq DNA polymerase (New England Biolabs).…”
Section: Phylogenetic Analysismentioning
confidence: 99%
“…Reactions for ndhF PCR products were mixed with 0.15 volume of 3 M sodium acetate, pH 4.6 and 3 volumes 95% (v/v) ethanol and subsequently purified by centrifuging at 4°C. Amplicons were then sent to Macrogen (Geumchun-gu, Seoul, Korea; http://www.macrogen.com) to be sequenced, using the respective PCR primers and additional internal primers for ndhF (ndhF599: 5′ TAGGTCTTTATTGGATAAC 3′; ndhF989-R: 5′ TGATGTTAGCTCTAGGATGTATGGG 3′; and ndhF1354: 5′ AAATGTCCTTCAAAAGTAAG 3′; Olmstead and Sweere, 1994) as well as for trnT-L regions (tabB: 5′TCTACCGATTTCGCCATATC 3′; and tabC: 5′ CGAAATCGGTAGACGCTACG 3′; Taberlet & al., 1991).…”
Section: Phylogenetic Analysismentioning
confidence: 99%
“…We used the primers 972F and 2110R described by Olmstead & Sweere (1994) to amplify the 3' half of ndhF. The PCR reactions included 25 µl total (2.5 µl 10X buffer, 5.0 µ l Q solution (Qiagen), 1.0 µl MgCl 2 (25mM), 1.0 µ l dNTPs (25mM), 1 µl each for the F and R primers (10mM), 0.2 µl Taq polymerase, 1.0 ul DNA template, and 11.3 ul of ddH20), with the following conditions: denaturation at 94°C for 4 min, followed by 30 cycles of denaturation at 94°C for 45 s, annealing at 49°C for 90 s, and extension at 72°C for 3 min, with a final extension step at 72°C for 7 min.…”
Section: Phylogenetic Analysis Based On Molecular Datamentioning
confidence: 99%
“…For example, a comparison between Cladosporium, Penicillium and Fusarium species at the NCBI Genome and GenBank databases (Schoch et al, 2012) will confirm this statement. Such considerations suggested that phylogenetic trees based on sets of genes are potentially more powerful in solving species boundaries than phylogenetic trees based on any single genes, as the former trees contain information about the simultaneous evolution of various biological processes (Olmstead & Sweere, 1994; Rokas et al, 2003). …”
Section: Introductionmentioning
confidence: 99%