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首页> 外文期刊>Genomics >Transcriptome profiling of early developing cotton fiber by deep-sequencing reveals significantly differential expression of genes in a fuzzless/lintless mutant.
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Transcriptome profiling of early developing cotton fiber by deep-sequencing reveals significantly differential expression of genes in a fuzzless/lintless mutant.

机译:通过深度测序对发育中的棉纤维进行转录组分析,揭示了无绒/无绒突变体中基因的显着差异表达。

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摘要

Cotton fiber as a single-celled trichome is a biological model system for studying cell differentiation and elongation. However, the complexity of its gene expression and regulatory mechanism allows only marginal progress. Here, we report the high-throughput tag-sequencing (Tag-seq) analysis using Solexa Genome Analyzer platform on transcriptome of -2 to 1 (fiber initiation, stage I) and 2-8 (fiber elongation, stage II) days post anthesis (DPA) cotton (Gossypium hirsutum) ovules (wild type: WT; Xuzhou 142 and its mutant: fuzzless/lintless or flM, in the same background). To this end, we sequenced 3.5-3.8 million tags representing 0.7-1.0 million unique transcripts for each library (WT1, WT2, M1, and M2). After removal of low quality tags, we obtained a total of 2,973,104, 3,139,306, 2,943,654, and 3,392,103 clean sequences that corresponded to 357,852, 280,787, 372,952, and 382,503 distinct tags for WT1, WT2, M1, and M2, respectively. All clean tags were aligned to the publicly available cotton transcript database (TIGR, http://www.tigr.org). About 15% of the distinct tags were uniquely mapped to the reference genes, and 31.4% of existing genes were matched by tags. The tag mapping to the database sequences generated 23,854, 24,442, 23,497, and 19,957 annotated genes for WT1, WT2, M1, and M2 libraries, respectively. Analyses of differentially expressed genes revealed the substantial changes in gene type and abundance between the wild type and mutant libraries. Among the 20 most differentially expressed genes in WT1/M1 and WT2/M2 libraries were cellulose synthase, phosphatase, and dehydrogenase, all of which are involved in the fiber cell development. Overall, the deep-sequencing analyses demonstrate the high degree of transcriptional complexity in early developing fibers and represent a major improvement over the microarrays for analyzing transcriptional changes on a large scale.
机译:棉花纤维作为单细胞毛状体是研究细胞分化和伸长的生物学模型系统。然而,其基因表达和调控机制的复杂性仅允许边际进展。在这里,我们报告了使用Solexa Genome Analyzer平台对开花后的-2至1(纤维起始,I期)和2-8(纤维伸长,II期)天的转录组进行高通量标签测序(Tag-seq)分析。 (DPA)棉花(陆地棉)胚珠(野生型:WT;徐州142及其突变体:无绒/无绒或flM,背景相同)。为此,我们对每个库(WT1,WT2,M1和M2)的3.5-380万个标签进行了排序,这些标签代表0.7-1.0百万个唯一的转录本。删除低质量标签后,我们获得了总共2,973,104、3,139,306、2,943,654和3,392,103个干净序列,分别对应于WT1,WT2,M1和M2的357,852、280,787、372,952和382,503个不同的标签。所有清洁标签均与公开的棉花成绩单数据库(TIGR,http://www.tigr.org)对齐。大约15%的独特标签被唯一地映射到参考基因,而31.4%的现有基因被标签匹配。映射到数据库序列的标签分别为WT1,WT2,M1和M2库生成了23,854、24,442、23,497和19,957个带注释的基因。差异表达基因的分析揭示了野生型和突变型文库之间基因类型的显着变化和丰度。 WT1 / M1和WT2 / M2文库中20个差异最大的基因是纤维素合酶,磷酸酶和脱氢酶,所有这些都参与了纤维细胞的发育。总体而言,深度测序分析表明,早期发育的纤维具有高度的转录复杂性,并且相对于用于大规模分析转录变化的微阵列而言,代表了重大改进。

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