2007
DOI: 10.1016/j.gene.2006.07.041
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The DcMaster Transposon Display maps polymorphic insertion sites in the carrot (Daucus carota L.) genome

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Cited by 31 publications
(27 citation statements)
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“…DNA restriction with MseI, ligation of adaptors, as well as preselective and selective PCR amplification were performed as described previously (Grzebelus et al 2007). Six different combinations of 3 selective nucleotides at the 3' end of the adaptor-specific primers (Table 2) were used for the final round of amplification.…”
Section: Identification Of Dcmtd Markersmentioning
confidence: 99%
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“…DNA restriction with MseI, ligation of adaptors, as well as preselective and selective PCR amplification were performed as described previously (Grzebelus et al 2007). Six different combinations of 3 selective nucleotides at the 3' end of the adaptor-specific primers (Table 2) were used for the final round of amplification.…”
Section: Identification Of Dcmtd Markersmentioning
confidence: 99%
“…Grzebelus et al (2007) reported that around 70% of DcMTD amplification products were polymorphic between the cultivated carrot line B493 and the wild carrot QAL. In the present study we obtained a similar, or even slightly higher level of polymorphism, reaching 79%.…”
Section: Dcmtd Markers As a Tool For Evaluation Of Genetic Diversitymentioning
confidence: 99%
“…Moreover, they can serve as useful tools for the functional genomics of model and crop plant species. While the application of transposable elements generally uses well characterised elements, such as Ac/Ds from maize, for mutagenesis in heterologous systems, endogenous elements can also be used as "tags" to clone genes or as markers for evaluating linkage analyses in progeny of genetic crosses (Ramachandran and Sundaresan 2001;Queen et al 2004;Grzebelus et al 2007). Therefore, while of interest in their own right, members of these classes of transposable elements in cassava may have the potential to assist with the genetic characterisation or improvement of this important crop.…”
Section: Discussionmentioning
confidence: 99%
“…Of these, 15 markers were included in the carrot reference linkage map, constructed previously using an F 2 population derived from a cross between the dark orange inbred B493 and a wild white-rooted carrot Queen Anne's Lace (QAL) Simon 2002, 2004;Grzebelus et al 2007;Just et al 2007;Cavagnaro et al 2009Cavagnaro et al , 2010. These markers were distributed across all nine linkage groups (Grzebelus et al 2007;Just et al 2007;Cavagnaro et al 2009Cavagnaro et al , 2010 and included eight STS markers (based on putative carotenoid biosynthetic gene sequences), four simple sequence repeats (SSRs), one sequencecharacterized amplified region (SCAR), and two PCR markers (for Rs and DCOR sequences; Table 1). In addition, two other markers from different carrot linkage maps were used to screen the BAC library and develop potential FISH probes.…”
Section: Methodsmentioning
confidence: 99%
“…The developed chromosome-specific carrot BACs provided us a tool to localize additional DNA sequences that were either not mapped or mapped in genetic backgrounds unrelated to the B493×QAL population used to construct the reference linkage map Simon 2002, 2004;Grzebelus et al 2007;Just et al 2007;Cavagnaro et al 2010). Thus, we were able to assign chromosomal positions to the rDNA gene clusters, and to six BAC probes (four unanchored and Table 1.…”
Section: Fish Mapping Of Additional Dna Sequencesmentioning
confidence: 99%