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Characterization of a drought inducible trithorax-like H3K4 methyltransferase from barley
被引:15
作者:
Papaefthimiou, D.
[1
,2
]
Tsaftaris, A. S.
[1
,3
]
机构:
[1] CERTH, Inst Agrobiotechnol, GR-57001 Thermi, Greece
[2] Aristotle Univ Thessaloniki, Dept Pharmaceut Sci, GR-54124 Thessaloniki, Greece
[3] Aristotle Univ Thessaloniki, Dept Genet & Plant Breeding, GR-54124 Thessaloniki, Greece
关键词:
Arabidopsis thaliana;
ATX;
Brachypodium distachyon;
epigenetic modifications;
histone;
HKMT;
Hordeum vulgare;
Oryza sativa;
EPIGENETIC CHROMATIN MODIFIERS;
HISTONE H3;
SEED DEVELOPMENT;
GENOME EVOLUTION;
DNA METHYLATION;
WATER-STRESS;
CPG ISLANDS;
GENE;
PLANTS;
IDENTIFICATION;
D O I:
10.1007/s10535-012-0125-z
中图分类号:
Q94 [植物学];
学科分类号:
071001 ;
摘要:
Histone H3 lysine 4 methylations catalyzed by histone lysine methyltransferases (HKMTs), like the Arabidopsis thaliana ATX1 and ATX2, are important epigenetic modifications related to chromatin decondensation and gene activation. In order to study this epigenetic mechanism in monocot cereal plants, we performed homology searches of ATX1 and ATX2 against the Brachypodium distachyon L. Beauv and rice (Oryza sativa L. spp. japonica) genomes, discovering single homologues for each cereal crop representing both Arabidopsis sequences. Using this information, we employed the rolling circle amplification - rapid amplification of cDNA ends (RCA-RACE) method to isolate, clone and characterize HvTX1 from RNA extracted from barley (Hordeum vulgare L.) tissues and studied its expression during seed development and under drought stress. The cloned cDNA sequence contained a 3 093 bp ORF homologous to ATX1 and ATX2. Characterization of the translated HvTX1 transcript sequence revealed the multi-domain nature of the putative protein, including all conserved regions characteristic for ATX1 and ATX2. By comparative genomic analysis and homology searches in EST databases we located, with high probability, the gene coding for HvTX1 on the barley chromosome 5H. Constant elevation of HvTX1 expression was observed during seed development. Expression of HvTX1 after drought stress was analyzed by quantitative real-time polymerase chain reaction (qPCR) in two different barley cultivars with varying drought stress tolerance, revealing HvTX1 drought-induction in a tolerance-specific manner.
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页码:683 / 692
页数:10
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