2001
DOI: 10.1007/s001220051695
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Genetic mapping of expressed sequence tag polymorphism (ESTP) markers in loblolly pine (Pinus taeda L.)

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Cited by 72 publications
(46 citation statements)
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“…Only selection on polymorphic genes involved in the traits will provide genetic gains from breeding population. Genetic mapping with genes of known function [17] and the test of their possible co-localisation with QTLs should be investigated. Comparative genome mapping will also allow to suspect QTLs in some genomic regions from results obtained in other species [17].…”
Section: Discussionmentioning
confidence: 99%
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“…Only selection on polymorphic genes involved in the traits will provide genetic gains from breeding population. Genetic mapping with genes of known function [17] and the test of their possible co-localisation with QTLs should be investigated. Comparative genome mapping will also allow to suspect QTLs in some genomic regions from results obtained in other species [17].…”
Section: Discussionmentioning
confidence: 99%
“…Genetic mapping with genes of known function [17] and the test of their possible co-localisation with QTLs should be investigated. Comparative genome mapping will also allow to suspect QTLs in some genomic regions from results obtained in other species [17]. Marker-assisted selection efficiency will be further tested in forest tree species.…”
Section: Discussionmentioning
confidence: 99%
“…PCR amplification was performed using primer pairs designed from these loci [20][21][22]26], which targeted the intron and/or 3' un-translated region [20] of the selected gene fragments. Of the screened 21 primer pairs, 15 (71%) produced single and clear PCR products ranging from 211 to 918 bp (Table 2); while the remaining 6 (29%) were produced multiple PCR products or no PCR amplifications.…”
Section: Resultsmentioning
confidence: 99%
“…The extracted DNA was further purified by MagneSil-Red (Promega) based on the manufacturer's instructions. Based on previously published low-copy anchored loci in Pinaceae [20][21][22]26], 21 loci were initially screened. PCR reactions were performed in a total volume of 10 L containing 1 × PCR buffer (Invitrogen), 1.5 mM MgCl 2 , 0.2 mM each dNTP, approximately 20 ng of template DNA and 0.25 U Platinum Taq DNA polymerase (Invitrogen).…”
Section: Sample and Dna Extractionmentioning
confidence: 99%
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