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The NIN transcription factor coordinates CEP and CLE signaling peptides that regulate nodulation antagonistically

机译:NIN转录因子协调拮抗调节结节的CEP和CLE信号肽

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摘要

Expression analysis of genes in wild-type (WT) roots 1 day post rhizobial inoculation (1 dpi). qRT-PCR was used to measure the gene expression levels, normalized relative to uninoculated roots. To highlight fold changes, the dotted line corresponds to a ratio of 1. Data points from four biological replicates are plotted as open circles (  = 8). Expression analysis of genes in WT roots in response to a Nod factor (NF) 10  M treatment for 3 h. qRT-PCR was used to measure the expression levels in treated roots. The results were normalized relative to untreated roots. To highlight fold changes, the dotted line corresponds to a ratio of 1. Data points from six biological replicates are plotted as open circles (  ≥ 11). Expression analysis of genes in WT roots in response to a cytokinin (BAP 10  M) treatment for 3 h. qRT-PCR was used to measure the gene expression levels in treated roots. The results were normalized relative to untreated roots. To highlight fold changes, the dotted line corresponds to a ratio of 1. Data points from four biological replicates are plotted as open circles (  ≥ 8). In – , center lines show the medians; box limits indicate the 25th and 75th percentiles as determined by the R software; whiskers extend 1.5 times the interquartile range from the 25th and 75th percentiles, outliers are represented by dots; and crosses represent sample means. Mann–Whitney test was used for each gene to assess significant differences between treated and control conditions, as indicated by asterisks (*  α α
机译:根瘤菌接种(1 dpi)1天后野生型(WT)根中基因的表达分析。使用qRT-PCR测量相对于未接种根部标准化的基因表达水平。为了突出显示倍数变化,虚线对应的比率为1。四个生物学重复的数据点绘制为空心圆(= 8)。响应3d h的Nod因子(NF)10μM处理,WT根中基因的表达分析。 qRT-PCR用于测量处理过的根中的表达水平。相对于未处理的根将结果标准化。为了突出显示倍数变化,虚线对应的比率为1。六个生物学重复的数据点绘制为空心圆(≥11)。细胞分裂素(BAP 10μM)处理3 h​​后,WT根中基因的表达分析。 qRT-PCR用于测量处理过的根中的基因表达水平。相对于未处理的根将结果标准化。为了突出显示倍数变化,虚线对应的比率为1。四个生物学重复的数据点绘制为空心圆(≥8)。在–中,中心线显示中位数;方框限制表示由R软件确定的第25和第75个百分点;晶须从第25个百分位数和第75个百分位数延伸四分位数间距的1.5倍,离群值由点表示;叉号代表样本均值。如星号所示,对每个基因进行了Mann-Whitney检验,以评估治疗和对照条件之间的显着差异。

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