2017
DOI: 10.1007/s11557-017-1322-0
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New insights in Russula subsect. Rubrinae: phylogeny and the quest for synapomorphic characters

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Cited by 35 publications
(21 citation statements)
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“…The mtSSU region was amplified using the primer pair MS1 and MS2 (White et al 1990). The rpb2 was amplified using the primers A-Russ-F-frpb2-7CR (Matheny 2005, Caboň et al 2017. All three molecular markers were amplified with Hot Start Firepol Polymerase (Solis Biodyne, Tartu, Estonia) using cycling protocols according to Caboň et al (2017).…”
Section: Molecular Analysismentioning
confidence: 99%
See 1 more Smart Citation
“…The mtSSU region was amplified using the primer pair MS1 and MS2 (White et al 1990). The rpb2 was amplified using the primers A-Russ-F-frpb2-7CR (Matheny 2005, Caboň et al 2017. All three molecular markers were amplified with Hot Start Firepol Polymerase (Solis Biodyne, Tartu, Estonia) using cycling protocols according to Caboň et al (2017).…”
Section: Molecular Analysismentioning
confidence: 99%
“…The rpb2 was amplified using the primers A-Russ-F-frpb2-7CR (Matheny 2005, Caboň et al 2017. All three molecular markers were amplified with Hot Start Firepol Polymerase (Solis Biodyne, Tartu, Estonia) using cycling protocols according to Caboň et al (2017). The PCR products were purified using Exo-Sap enzymes (Thermo Fisher Scientific, Wilmington, DE) or the Qiaquick PCR Purification Kit (Qiagen, Hilden, Germany).…”
Section: Molecular Analysismentioning
confidence: 99%
“…We targeted five DNA regions: (1) the internal transcribed spacer regions of nuclear ribosomal DNA (ITS); (2) partial large subunit of nuclear ribosomal DNA (LSU); (3) partial mitochondrial small subunit of ribosomal DNA (mtSSU); (4) the region between domains six and seven of the nuclear gene encoding the second largest subunit of RNA polymerase II ( rpb2 ); (5) part of the translation elongation factor 1-alpha ( tef1α ). The following primer pairs were used for the DNA amplifications: ITS1F–ITS4 for ITS [ 22 , 23 ], LR0R–LR5 for LSU [ 24 ], MS1–MS2 for mtSSU [ 22 ], A-Russ-F–frpb2-7CR for rpb2 [ 25 , 26 ], EF1-983F–EF1-1567R for tef1α [ 27 ]. All molecular markers were amplified with 5× HOT FIREPol ® Blend Master Mix (Solis BioDyne, Tartu, Estonia) applying PCR conditions of Caboň et al [ 26 ].…”
Section: Methodsmentioning
confidence: 99%
“…The following primer pairs were used for the DNA amplifications: ITS1F–ITS4 for ITS [ 22 , 23 ], LR0R–LR5 for LSU [ 24 ], MS1–MS2 for mtSSU [ 22 ], A-Russ-F–frpb2-7CR for rpb2 [ 25 , 26 ], EF1-983F–EF1-1567R for tef1α [ 27 ]. All molecular markers were amplified with 5× HOT FIREPol ® Blend Master Mix (Solis BioDyne, Tartu, Estonia) applying PCR conditions of Caboň et al [ 26 ]. The PCR products were purified using Exo-Sap enzymes (Thermo Fisher Scientific, Wilmington, Germany) and sequenced at SeqMe sequencing company (Dobříš, Czech Republic).…”
Section: Methodsmentioning
confidence: 99%
“…There are relatively fewer researches in which multiple genes were analysed, e.g. ITS, mtSSU, nLSU and rpb2 in Li et al (2010b), ITS, nLSU and rpb2 in Park et al (2013), ITS and nLSU in Park et al (2014), ITS, rpb2, atp6, cox3 and chsi in Cao et al (2013) and ITS, mtSSU and rpb2 in Caboň et al (2017). In the present study, six genes, namely nLSU (28S), ITS, tef-1α, mtSSU, rpb1, and rpb2, which have been widely analysed in molecular phylogeny, were selected as candidate biomarkers.…”
Section: Introductionmentioning
confidence: 99%