2004
DOI: 10.1111/j.1471-8286.2004.00636.x
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Universal primers for the amplification of chloroplast microsatellites in grasses (Poaceae)

Abstract: Attempts to design truly universal primers to amplify chloroplast microsatellites have met with limited success due to nonconservation of repeat loci across widely divergent taxa. We have used the complete chloroplast genome sequences of rice, maize and wheat to design five pairs of primers that amplify homologous mononucleotide repeats across the Poaceae (grasses). Sequencing confirmed conservation of repeat motifs across subfamilies and a preliminary study in Anthoxanthum odoratum revealed polymorphism at tw… Show more

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Cited by 42 publications
(33 citation statements)
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“…To estimate F st(cp) , we used three polymorphic cp microsatellite markers (WCt5, atpB/rbcL and rpoC2/ rps2; Ishii and McCouch, 2000;Provan et al, 2004) to haplotype a total of 55 Anthoxanthum plants sampled from either ends of the transect crossing the 8/9-1 boundary and from control (unfertilized) Plot 12. PCR was carried out in 20 ml reactions containing 1-2 ml template DNA, 5 pmol of each primer, 200 mM of each dNTP, standard buffer (supplied with the Taq) containing 1.5 mM MgCl 2 and 1 U of Taq DNA polymerase in a Techne Genius thermal cycler using the following profile: initial denaturation for 4 min at 941C, followed by 35 cycles of 941C for 1 min, 551C for 1 min, 721C for 2 min and a final extension for 5 min at 721C.…”
Section: Gene Flowmentioning
confidence: 99%
“…To estimate F st(cp) , we used three polymorphic cp microsatellite markers (WCt5, atpB/rbcL and rpoC2/ rps2; Ishii and McCouch, 2000;Provan et al, 2004) to haplotype a total of 55 Anthoxanthum plants sampled from either ends of the transect crossing the 8/9-1 boundary and from control (unfertilized) Plot 12. PCR was carried out in 20 ml reactions containing 1-2 ml template DNA, 5 pmol of each primer, 200 mM of each dNTP, standard buffer (supplied with the Taq) containing 1.5 mM MgCl 2 and 1 U of Taq DNA polymerase in a Techne Genius thermal cycler using the following profile: initial denaturation for 4 min at 941C, followed by 35 cycles of 941C for 1 min, 551C for 1 min, 721C for 2 min and a final extension for 5 min at 721C.…”
Section: Gene Flowmentioning
confidence: 99%
“…Chloroplast microsatellites were chosen to determine demographic histories as they are nonrecombining, haploid and effectively uni-parentally inherited (Birky, 1995), providing direct evidence of a lineage. The availability of 'universal primers' for highly conserved primer sites on either side of polymorphic repeat regions has made such analyses possible (Provan et al, 2004;McGrath et al, 2006).…”
Section: Methodsmentioning
confidence: 99%
“…A total of 10 non-coding microsatellites were tested from those developed by McGrath et al (2006) and Provan et al (2004), from which only four, trnK, atpI/atpH, atpB/rbcL and TeaSSR4 (23S-5S internal transcribed spacer), were able to be amplified. Only the last three had polymorphic alleles and were used in the analysis.…”
Section: Microsatellitesmentioning
confidence: 99%
“…In 2003, Chung and Staub designed 23 pairs of cpSSRs consensus primers that amplify targeted regions in a diverse array of plant species. Recently, Provan et al (2004a) developed five pairs of universal primers for the amplification of cpSSRs in grasses (Poaceae). More recently, Cheng et al (2006) developed a set of universal cpSSR primers to explore cpDNA diversity among sub-tropical and tropical fruit crops, where cpDNA sequences are unknown.…”
Section: Universal Primers That Target the Chloroplast Simple Sequencmentioning
confidence: 99%