2002
DOI: 10.1016/s0965-1748(01)00164-3
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Evolution and phylogenetic information content of the ribosomal DNA repeat unit in the Blattodea (Insecta)

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Cited by 28 publications
(27 citation statements)
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“…The amplified rDNA regions contained the ITS1 (261–388 bp) and ITS2 (188–262 bp) regions, the 5.8S gene (157 bp), and approximately 200 and 1000 bp of the 18S and 28s genes, respectively. The amplification was performed in 50  μ L reactions using a PCR Master Mix (2X) (Fermentas, Vilnius, Lithuania) according to the manufacturer's instructions; the reactions were performed in a Primus 25 advanced Thermocycler (PEQLAB, Erlangen, Germany) using previously published rDNA-specific parameters [98]. The PCR products were resolved on 1.0% agarose gels, and DNA was extracted from the observed unique bands using the QIAquick Gel Extraction Kit (QIAGEN, Hilden, Germany).…”
Section: Methodsmentioning
confidence: 99%
“…The amplified rDNA regions contained the ITS1 (261–388 bp) and ITS2 (188–262 bp) regions, the 5.8S gene (157 bp), and approximately 200 and 1000 bp of the 18S and 28s genes, respectively. The amplification was performed in 50  μ L reactions using a PCR Master Mix (2X) (Fermentas, Vilnius, Lithuania) according to the manufacturer's instructions; the reactions were performed in a Primus 25 advanced Thermocycler (PEQLAB, Erlangen, Germany) using previously published rDNA-specific parameters [98]. The PCR products were resolved on 1.0% agarose gels, and DNA was extracted from the observed unique bands using the QIAquick Gel Extraction Kit (QIAGEN, Hilden, Germany).…”
Section: Methodsmentioning
confidence: 99%
“…Use of PCR as a tool to amplify and sequence genes and then exploit the nucleotide data for phylogenetic analysis and develop evolutionary relationships among grasshopper species has previously been practiced by a number of researchers (Colgan 1991;Chapco & Litzenberger 2003;Rowell & Flook 2004). Several researchers have used DNA data in phylogenetic analysis to identify grasshopper species (Chapco & Litzenberger 2002;Mukha et al 2001;Song & Wenzel (2007) Ketmaier et al 2010). Use of DNA data has also been used in combination with morphological data to establish species relationships (Brust 2008 Kirby (1914), Fletcher (1919, Mahmood (1995), Mahmood & Yousaf (1999), Mahmood & Yousaf (2000); ; Azim & Reshi (2010) but nobody has made any effort to identify them on a molecular level either by DNA barcoding or by using any other marker.…”
Section: Introductionmentioning
confidence: 99%
“…On the other hand, comparisons among ribosomal DNA internal transcribed spacer (rDNA ITS) sequences have been helpful to ascertain evolutionary relatedness of closely related species in diverse insect groups, owing to their high evolutionary rates (Vogler and DeSalle, 1994;Schlötterer et al, 1994: Di Muccio et al, 2000Weekers et al, 2001, Mukha et al, 2002. Recently, studies of Coleoptera and Hemiptera demonstrated the usefulness of ITS-1 and ITS-2 markers in discovering phylogenetic relationships at higher levels such as tribe and subfamily (Marcilla et al, 2001;Von der Schulenburg, 2001).…”
Section: Introductionmentioning
confidence: 99%