Articles
SEARCH FOR MOLECULAR MARKERS LINKED TO FIRE BLIGHT RESISTANCE IN PEAR (PYRUS COMMUNIS)
Article number
704_89
Pages
557 – 566
Language
English
Abstract
Randomly amplified polymorphic DNA (RAPD) and resistance gene analog (RGA) were used to search for molecular markers linked to fire blight resistance in Pyrus communis) Old Home and Seckel. Genomic DNA from these fire blight resistant cultivars and the susceptible Bartlett were used as templates.
To obtain RGAs, degenerate primers based on conserved regions in NBS-LRR and protein kinase-type resistance genes were used to amplify bands of ~550 and ~600 bp, respectively, from Old Home and Seckel. Cloning and sequencing twenty of these PCR products revealed that all had different sequences, and all, except for two, of the clones were similar to RGAs from other plant species and had high similarity to several R genes.
Parsimony analysis of the predicted protein sequences of the pear RGAs and their most similar characterized R genes showed that pear RGAs clustered with known R genes.
Sequence characterized amplified region (SCAR) primers designed from these RGA sequences revealed no PCR length polymorphisms.
Sequencing two PCR products from Bartlett showed that they had ~98% identity to the original sequences from Seckel. RAPD analyses of Bartlett, Seckel and Old Home revealed a high similarity (~92-93%) between the three cultivars.
Four polymorphic PCR products were cloned and sequenced, and RAPD-SCAR primers were designed.
No PCR length polymorphisms were found, and sequencing of a PCR product from Bartlett and Seckel using the same RAPD-SCAR primer pair showed that they had 90% nucleotide identity.
These results show some of the challenges in finding markers linked to fire blight resistance among different pear cultivars, which have a high degree of similarity to one another.
To obtain RGAs, degenerate primers based on conserved regions in NBS-LRR and protein kinase-type resistance genes were used to amplify bands of ~550 and ~600 bp, respectively, from Old Home and Seckel. Cloning and sequencing twenty of these PCR products revealed that all had different sequences, and all, except for two, of the clones were similar to RGAs from other plant species and had high similarity to several R genes.
Parsimony analysis of the predicted protein sequences of the pear RGAs and their most similar characterized R genes showed that pear RGAs clustered with known R genes.
Sequence characterized amplified region (SCAR) primers designed from these RGA sequences revealed no PCR length polymorphisms.
Sequencing two PCR products from Bartlett showed that they had ~98% identity to the original sequences from Seckel. RAPD analyses of Bartlett, Seckel and Old Home revealed a high similarity (~92-93%) between the three cultivars.
Four polymorphic PCR products were cloned and sequenced, and RAPD-SCAR primers were designed.
No PCR length polymorphisms were found, and sequencing of a PCR product from Bartlett and Seckel using the same RAPD-SCAR primer pair showed that they had 90% nucleotide identity.
These results show some of the challenges in finding markers linked to fire blight resistance among different pear cultivars, which have a high degree of similarity to one another.
Publication
Authors
M.R. Afunian, P.H. Goodwin, D.M. Hunter
Keywords
RAPD, resistance gene analogs, SCAR, NBS-LRR
Online Articles (93)

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