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首页> 外文期刊>Czech Journal of Genetics and Plant Breeding >Characterization and expression of high temperature stress responsive genes in bread wheat ( Triticum aestivum L.)
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Characterization and expression of high temperature stress responsive genes in bread wheat ( Triticum aestivum L.)

机译:面包小麦中高温胁迫响应基因的表征与表达

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To elucidate the effects of high temperatures, wheat plants ( Triticum aestivum cv. CPAN 1676) were given heat shocks at 37°C and 42°C for two hours, and responsive genes were identified through PCR-Select Subtraction technology. Four subtractive cDNA libraries, including three forward and one reverse subtraction, were constructed from three different developmental stages. A total of 5500 ESTs were generated and 3516 high quality ESTs were submitted to Genbank. More than one third of the ESTs generated fall in unknowno hit categories upon a homology search through BLAST analysis. A large number of high temperature responsive genes have been identified and characterized. Reverse subtraction analysis in developing grains showed extensive transcriptional changes upon heat stress as revealed by comparative analysis with forward subtraction. Differential expression was confirmed by cDNA macroarray and by northern/RT-PCR analysis. Expression analysis of wheat plants subjected to high temperature stress, after one and four days of recovery, showed fast recovery in seedling tissues. However, recovery was small in the developing seed tissue after two hours of heat stress. Ten selected genes were analysed in further detail by quantitative real-time PCR in an array of 35 different wheat tissues representing major developmental stages as well as different abiotic stresses. Tissue specificity was examined along with cross talk with other abiotic stresses and putative signalling molecules. The results obtained contribute towards understanding the regulation of genes at different developmental stages in wheat crucial to withstanding and recovery from heat stress.
机译:为了阐明高温的影响,在37°C和42°C下对小麦植物(Triticum aestivum cv。CPAN 1676)进行了两个小时的热激,并通过PCR-Select Subtraction技术鉴定了响应基因。从三个不同的发育阶段构建了四个减法cDNA文库,包括三个正向和一个反向减法。总共生成了5500个EST,并向Genbank提交了3516个高质量的EST。通过BLAST分析进行同源性搜索后,产生的EST中有超过三分之一属于未知/无命中类别。已经鉴定和表征了许多高温响应基因。通过正向减法的比较分析可以看出,发育中谷物的反向减法分析显示了在热胁迫下的大量转录变化。通过cDNA大阵列和Northern / RT-PCR分析证实了差异表达。恢复一到四天后,遭受高温胁迫的小麦植物的表达分析显示出幼苗组织中的快速恢复。但是,经过两个小时的热应激,发育中的种子组织的恢复很小。通过定量实时PCR在代表主要发育阶段以及不同非生物胁迫的35种不同小麦组织的阵列中,通过定量实时PCR进一步详细分析了10个选定基因。检查组织特异性以及与其他非生物胁迫和推定的信号分子的串扰。获得的结果有助于理解小麦不同发育阶段的基因调控,这对于抵御热胁迫和从热胁迫中恢复至关重要。

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