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Disease resistance gene homologs correlate with disease resistance loci of Arabidopsis thaliana
Author(s) -
Speulman Elly,
Bouchez David,
Holub Eric B.,
Bey Jim L.
Publication year - 1998
Publication title -
the plant journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 3.058
H-Index - 269
eISSN - 1365-313X
pISSN - 0960-7412
DOI - 10.1046/j.1365-313x.1998.00138.x
Subject(s) - arabidopsis , genetics , biology , gene , arabidopsis thaliana , plant disease resistance , r gene , cloning (programming) , conserved sequence , peptide sequence , mutant , computer science , programming language
Summary The disease resistance genes RPS2 of Arabidopsis and N of tobacco, among other recently cloned resistance genes, share several conserved sequences. Degenerate oligonucleotide primers, based on conserved sequences in the nucleotide binding site (NBS) and a weak hydrophobic domain of RPS2 and N , were used to amplify homologous sequences from Arabidopsis thaliana . Amplification products were obtained that were similar in sequence to the disease resistance genes RPS2 , RPM1 , N and L6 . The Arabidopsis CIC‐YAC library was used to identify the position of the disease resistance homologs on the Arabidopsis genome. Their map positions could be correlated with the disease resistance loci RPS5, RAC1, RPP9, CAR1, RPP7, RPW2, RPP1, RPP10, RPP14, RPP5, RPP4, RPS2, RPW6, HRT, RPS4, RPP8, RPP21, RPP22, RPP23, RPP24 and TTR1 . This method was therefore not only successful in the identification of sequences located within gene clusters that are involved in disease resistance, but could also contribute to the cloning of disease resistance genes from Arabidopsis .

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