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Genome-Wide Phylogenetic Analysis of Stress-Activated Protein Kinase Genes in Rice (OsSAPKs) and Expression Profiling in Response to Xanthomonas oryzae pv. oryzicola Infection
All members of the SnRK2 protein kinase gene family encoded by the rice ( Oryza sativa L.) genome are activated by hyperosmotic stress, and have been designated as stress-activated protein kinases (SAPKs). In this study, gene structures, phylogeny, and conserved motifs for the entire OsSAPK gene fam...
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Published in: | Plant molecular biology reporter 2013-08, Vol.31 (4), p.877-885 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | All members of the SnRK2 protein kinase gene family encoded by the rice (
Oryza sativa
L.) genome are activated by hyperosmotic stress, and have been designated as stress-activated protein kinases (SAPKs). In this study, gene structures, phylogeny, and conserved motifs for the entire OsSAPK gene family in rice have been analyzed. Moreover, expression patterns of OsSAPK in response to infection with
Xanthomonas oryzae
pv.
oryzicola
(
Xoc
) were investigated. A total of ten
OsSAPK
genes in the
japonica
rice cultivar 9804 were identified and classified into four groups. All genes had similar exon–intron structures and organization of putative motifs/domains, and shared the same four motifs (motifs 1–4). Group I (OsSAPK1 and OsSAPK2) shared another two motifs (motif 5 and motif 10), while group III (OsSAPK8, OsSAPK9 and OsSAPK10) had seven motifs in common (motifs 1–7). Moreover, we found that four
OsSAPKs
, including
OsSAPK3
,
OsSAPK5
,
OsSAPK7
and
OsSAPK9
, were significantly upregulated in response to infection by
Xoc
in rice plants carrying the nonhost resistance gene
Rxo1
. Four of the
OsSAPK
genes in which expression was upregulated were localized to both the cytoplasm and nucleus, but clustered in different groups, suggesting that they are involved in different resistance signal transduction pathways. These results will provide useful information for the future functional dissection of this gene family. |
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ISSN: | 0735-9640 1572-9818 |
DOI: | 10.1007/s11105-013-0559-2 |