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首页> 外文期刊>Journal of Experimental Botany >Gene expression profiles for cell wall-modifying proteins associated with soybean cyst nematode infection, petiole abscission, root tips, flowers, apical buds, and leaves
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Gene expression profiles for cell wall-modifying proteins associated with soybean cyst nematode infection, petiole abscission, root tips, flowers, apical buds, and leaves

机译:与大豆囊肿线虫感染,叶柄脱落,根尖,花,顶端芽和叶相关的细胞壁修饰蛋白的基因表达谱

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摘要

Changes in transcript accumulation for cell wall-modifying proteins were examined in excised soybean root pieces colonized by soybean cyst nematodes (SCN), Heterodera glycines, using RT-PCR and soybean Affymetrix GeneChips. Sequence-specific PCR primer pairs were prepared from sequence data for core sequences in the GenBank soybean database and consensus sequences derived from the assembly of soybean ESTs. In addition, to identify previously uncharacterized soybean transcripts, degenerate primers were prepared for conserved motifs in cellulases (endo-1,4-β-glucanases, EGases) and polygalacturonases (PGs) and these were used to amplify segments of transcripts that were then extended with 3′ and 5′ RACE. Several novel EGase and PG transcripts were identified. Gene expression patterns were determined by real-time RT-PCR for 11 EGases, three expansins (EXPs), 14 PGs, two pectate lyases (PLs), and two xyloglucan endotransglucosylase/hydrolases (XTHs) in soybean roots inoculated with SCN, non-inoculated roots, serial dissections of root tips, leaf abscission zones, flowers, apical buds, and expanding leaves. A large number of genes associated with cell wall modifications are strongly up-regulated in root pieces colonized by SCN. However, in contrast to most of the transcripts for cell wall proteins, two XTH transcripts were specifically down-regulated in the colonized root pieces. Gene expression in serial dissections of root tips (0–2 mm, and 2–7 mm) and whole roots indicate that the SCN up-regulated genes are associated with a wide range of developmental processes in roots. Also of interest, many of the cDNAs examined were up-regulated in petiole abscission zones induced to abscise with ethylene.
机译:使用RT-PCR和大豆Affymetrix GeneChips,在由大豆囊肿线虫(SCN),异戊三烯甘氨酸定殖的切下的大豆根片中检测了细胞壁修饰蛋白的转录积累变化。根据GenBank大豆数据库中核心序列的序列数据和源自大豆EST装配的共有序列,制备了序列特异性PCR引物对。另外,为了鉴定以前未表征的大豆转录本,制备了简并引物用于纤维素酶(内切1,4-β-葡聚糖酶,EGases)和聚半乳糖醛酸酶(PGs)中的保守基序,并使用这些引物扩增转录本的片段,然后将其延伸3'和5'RACE。鉴定了几种新颖的EGase和PG转录物。通过实时逆转录-聚合酶链反应(RT-PCR)确定了用SCN接种的大豆根中11种EGase,3种扩展酶(EXP),14种PG,2种果胶裂解酶(PLs)和2种木葡聚糖内切葡糖苷酶/水解酶(XTH)的基因表达模式。接种根,根尖的连续解剖,叶脱落区,花,顶芽和扩张的叶子。与细胞壁修饰有关的大量基因在SCN定植的根中强烈上调。但是,与细胞壁蛋白的大多数转录本相反,两个XTH转录本在定植的根片中被特异性下调。根尖(0–2 mm和2–7 mm)和整个根部的连续解剖中的基因表达表明SCN上调的基因与根部的广泛发育过程相关。同样令人感兴趣的是,许多检测的cDNA在被乙烯诱导脱落的叶柄脱落区上调。

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