2002
DOI: 10.1016/s0304-4238(01)00358-2
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Defining the sources of Paradox: DNA sequence markers for North American walnut (Juglans L.) species and hybrids

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Cited by 51 publications
(33 citation statements)
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“…The ITS1-5.8S-ITS2 region was amplified with the primers ITS5_bryo and ITS4_bryo (Stech & Frahm, 1999), the trnL-F region with the primers trnC and trnF (Taberlet et al, 1991) and trnD-T with the primers trnD and trnT (Demesure, Sodzi & Petit, 1995). For some specimens the trnD-T region was sequenced in two pieces with primers trnD and trnY_F, and trnT and trnY_R (Huttunen & Ignatov, unpublished data) to avoid problems with the poly-A/T repeat at end of the trnE-Y spacer (Potter et al, 2002;Shaw et al, 2005). PCR cycles included an initial denaturation with 5 min at 95uC, followed by 35 cycles of 30 s 95uC, 30 s 52uC, 1 min 30 s 72uC for the ITS region, 30-35 cycles of 45 s 95uC, 30 s 52uC, 1 min 30 s 72uC for the trnD-T, and 35 cycles of 1 min 95uC, 1 min 52uC, 1 min 72uC for the trnL-F, and a final elongation of 8 min at 72uC.…”
Section: Molecular Methodsmentioning
confidence: 99%
“…The ITS1-5.8S-ITS2 region was amplified with the primers ITS5_bryo and ITS4_bryo (Stech & Frahm, 1999), the trnL-F region with the primers trnC and trnF (Taberlet et al, 1991) and trnD-T with the primers trnD and trnT (Demesure, Sodzi & Petit, 1995). For some specimens the trnD-T region was sequenced in two pieces with primers trnD and trnY_F, and trnT and trnY_R (Huttunen & Ignatov, unpublished data) to avoid problems with the poly-A/T repeat at end of the trnE-Y spacer (Potter et al, 2002;Shaw et al, 2005). PCR cycles included an initial denaturation with 5 min at 95uC, followed by 35 cycles of 30 s 95uC, 30 s 52uC, 1 min 30 s 72uC for the ITS region, 30-35 cycles of 45 s 95uC, 30 s 52uC, 1 min 30 s 72uC for the trnD-T, and 35 cycles of 1 min 95uC, 1 min 52uC, 1 min 72uC for the trnL-F, and a final elongation of 8 min at 72uC.…”
Section: Molecular Methodsmentioning
confidence: 99%
“…The ITS region of the nuclear DNA includes three components: internal transcribed spacer 1, the 5.8S ribosomal RNA gene, and internal transcribed spacer 2 (Baldwin 1992). Sequence diversity among ITS1 alleles has been used to distinguish closely related species and for phylogenetic studies in many angiosperm families and fungi (Baldwin et al 1995;Potter et al 2002). Because the ITS region is highly conserved intraspecifically but variable among species, it is often used in taxonomy (Liston et al 1999).…”
mentioning
confidence: 99%
“…The trnT UGU -trnF GAA region, like other regions of the chloroplast, has been used extensively in plant systematic to differentiate among taxa (Olmstead and Palmer 1994;Won and Renner 2005). There are only a few species-specific markers for the Juglandaceae (Germain et al 1993;Potter et al 2002;McCleary et al 2009). Now that the regeneration of butternut has become a pressing concern, there is a need to develop concomitant molecular methods to identify nonhybrid butternut (Ostry and Woeste 2004).…”
mentioning
confidence: 99%
“…Understanding the nature and origins of hybrids is important to breeders, ecologists, and taxonomists. DNA markers are the most commonly used molecular tools for identifying species and interspecific hybrids, and marker systems describing hybridization relevant to hardwood improvement have been described for Alnus (Prat 1988), Betula (Clausen 1979), Juglans (Potter et al 2002), Liriodendron (Wang 2003), Platanus (Santini 2001), Salix (Krstinic and Kajba 1997) Ulmus (Pinon et al 1999), and probably other genera as well.…”
Section: Molecular Marker Applicationsmentioning
confidence: 99%