首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >RNAi-mediated gene silencing reveals involvement of Arabidopsis chromatin-related genes in Agrobacterium-mediated root transformation
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RNAi-mediated gene silencing reveals involvement of Arabidopsis chromatin-related genes in Agrobacterium-mediated root transformation

机译:RNAi介导的基因沉默揭示了拟南芥染色质相关基因参与农杆菌介导的根转化

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摘要

We investigated the effect of RNAi-mediated gene silencing of 109 Arabidopsis thaliana chromatin-related genes (termed "chromatin genes" hereafter) on Agrobacterium-mediated root transformation. Each of the RNAi lines contains a single- or low-copy-number insertion of a hairpin construction that silences the endogenous copy of the target gene. We used three standard transient and stable transformation assays to screen 340 independent RNAi lines, representing 109 target genes, for the rat (resistant to Agrobac-terium transformation) phenotype. Transformation frequency was not affected by silencing 85 of these genes. Silencing of 24 genes resulted in either a weak or strong rat phenotype. The rat mutants fell into three general groups: (ⅰ) severely dwarfed plants exhibiting a strong rat phenotype (CHC1); (ⅱ) developmentally normal plants showing a reduced response to three transformation assays (HAG3, HDT1. HDA15, CHR1, HAC1, H0N5, HDT2, GTE2, GTE4, GTE7. HDA19, HAF1, NFA2, NFA3. SGA1, and SGB2); or (ⅲ) varying response among the three transformation assays (DMT1, DMT2, DMT4, SDG1, SDG1S, SDG22, and SDG29). A direct molecular assay indicated that SGA1, HDT1, and HDT2 are important for T-DNA integration into the host genome in Arabidopsis roots.
机译:我们调查了109拟南芥染色质相关基因(以下称为“染色质基因”)的RNAi介导的基因沉默对农杆菌介导的根转化的影响。每个RNAi品系均包含发夹结构的单拷贝或低拷贝数插入物,该插入物可沉默靶基因的内源性拷贝。我们使用三种标准的瞬时和稳定转化试验来筛选340个独立的RNAi系,它们代表109个靶基因(对Agrobac-terium转化具有抗性)。转化频率不受这些基因中85个基因沉默的影响。 24个基因的沉默导致弱或强大鼠表型。大鼠突变体分为三大类:(ⅰ)表现出强烈大鼠表型(CHC1)的严重矮化植物; (ⅱ)对三种转化试验(HAG3,HDT1,HDA15,CHR1,HAC1,H0N5,HDT2,GTE2,GTE4,GTE7,HDA19,HAF1,NFA2,NFA3,SGA1和SGB2)响应降低的发育正常植物;或(ⅲ)三种转化试验(DMT1,DMT2,DMT4,SDG1,SDG1S,SDG22和SDG29)之间的响应有所不同。直接分子分析表明,SGA1,HDT1和HDT2对于将T-DNA整合到拟南芥根中的宿主基因组中很重要。

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