2017
DOI: 10.1007/978-1-4939-7249-4_19
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MutRenSeq: A Method for Rapid Cloning of Plant Disease Resistance Genes

Abstract: MutRenSeq is a method to clone disease resistance (R) genes in plants. Tips and detailed experimental protocols for the pipeline, including the complexity reduction by R gene targeted enrichment sequencing, and computational analysis based on comparative genomics are provided in this chapter.

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Cited by 25 publications
(11 citation statements)
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“…In line with these data, research will have to fully consider comparative genomics within the Ma locus to identify the resistance determinants (sequences and/or motifs) and in particular, those involved in the resistance specificity. Methods and model studies published recently open the way in this objective [75][76][77]. The noteworthy C-terminal part of the gene with a huge post-LRR region (=5 repeated PL domains) makes it the longest R gene ever cloned.…”
Section: Discussionmentioning
confidence: 99%
“…In line with these data, research will have to fully consider comparative genomics within the Ma locus to identify the resistance determinants (sequences and/or motifs) and in particular, those involved in the resistance specificity. Methods and model studies published recently open the way in this objective [75][76][77]. The noteworthy C-terminal part of the gene with a huge post-LRR region (=5 repeated PL domains) makes it the longest R gene ever cloned.…”
Section: Discussionmentioning
confidence: 99%
“…Illumina libraries with an average insert size of 700□bp were enriched by Arbor Biosciences, Michigan, USA, as previously described 26 , and sequenced on an Illumina HiSeq with either 150 or 250 PE reads at Novogene, China to generate an average of 3.82 Gb per accession (Table S2). The raw reads were trimmed using Trimmomatic v0.2 27 and de novo assembled with the CLC Assembly Cell (http://www.clcbio.com/products/clc-assembly-cell/) using word size (-w□=□64) with standard parameters.…”
Section: Methodsmentioning
confidence: 99%
“…4). Another promising option would be to integrate genomic selection with rapid disease-resistance gene discovery and cloning technologies 48,49 . While marker-assisted selection can be used to transfer resistance genes with large effects, coupling the approach with genomic selection could help to accumulate and maintain minor gene variants that contribute to effective resistance.…”
Section: Review Articlementioning
confidence: 99%