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首页> 外文期刊>The New Phytologist >Identification of conserved core xylem gene sets: conifer cDNA microarray development, transcript profiling and computational analyses
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Identification of conserved core xylem gene sets: conifer cDNA microarray development, transcript profiling and computational analyses

机译:保守核心木质部基因集的鉴定:针叶树cDNA微阵列开发,成绩单分析和计算分析

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One approach for investigating the molecular basis of wood formation is to integrate microarray profiling data sets and sequence analyses, comparing tree species with model plants such as Arabidopsis. Conifers may be included in comparative studies thanks to large-scale expressed sequence tag (EST) analyses, which enable the development of cDNA microarrays with very significant genome coverage. A microarray of 10 400 low-redundancy sequences was designed starting from white spruce (Picea glauca (Moench.) Voss) cDNAs. Computational procedures that were developed to ensure broad transcriptome coverage and efficient PCR amplification were used to select cDNA clones, which were re-sequenced in the microarray manufacture process. White spruce transcript profiling experiments that compared secondary xylem to phloem and needles identified 360 xylem-preferential gene sequences. The functional annotations of all differentially expressed sequences were highly consistent with the results of similar analyses carried out in angiosperm trees and herbaceous plants. Computational analyses comparing the spruce microarray sequences and core xylem gene sets from Arabidopsis identified 31 transcripts that were highly conserved in angiosperms and gymnosperms, in terms of both sequence and xylem expression. Several other spruce sequences have not previously been linked to xylem differentiation (including genes encoding TUBBY-like domain proteins (TLPs) and a gibberellin insensitive (gai) gene sequence) or were shown to encode proteins of unknown function encompassing diverse conserved domains of unknown function.
机译:研究木材形成的分子基础的一种方法是整合微阵列分析数据集和序列分析,将树种与模型植物(如拟南芥)进行比较。得益于大规模表达序列标签(EST)分析,可以将针叶树纳入比较研究,从而开发具有非常重要的基因组覆盖率的cDNA微阵列。从白云杉(Picea glauca(Moench。)Voss)cDNAs开始设计了10400个低冗余序列的微阵列。为确保广泛的转录组覆盖和有效的PCR扩增而开发的计算程序用于选择cDNA克隆,并在微阵列制造过程中对其进行重新测序。比较了次生木质部与韧皮部和针的白云杉转录物谱分析实验,确定了360个木质部优先基因序列。所有差异表达序列的功能注释与被子植物和草本植物中进行的相似分析的结果高度一致。计算分析比较了来自拟南芥的云杉微阵列序列和核心木质部基因组,从序列和木质部表达两个方面,鉴定了31个在被子植物和裸子植物中高度保守的转录本。其他一些云杉序列以前未与木质部分化相关联(包括编码TUBBY样域蛋白(TLP)的基因和赤霉素不敏感(gai)基因序列)或已显示编码未知功能的蛋白质,包括功能未知的各种保守域。

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