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首页> 外文期刊>Plant Growth Regulation: An International Journal on Natural and Synthetic Regulators >Transcriptomic analysis of maize kernel row number-associated miRNAs between a single segment substitution line and its receptor parent
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Transcriptomic analysis of maize kernel row number-associated miRNAs between a single segment substitution line and its receptor parent

机译:单节替代系与其受体亲本之间与玉米籽粒行数相关的miRNA的转录组学分析

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摘要

To detect microRNAs (miRNAs) involved in determining kernel row number in maize, next generation deep sequencing was performed on an elite inbred line Zong3 (row number 14-16) of maize in China and a single segment substitution line (SSSL) SSL-10 (row number 8-10) derived from the same genetic background. In SSL-10, the single segment is inserted in chromosome 1 between molecular marker bnlg1953 and bnlg1811. Twenty-eight miRNAs belonging to 11 conserved miRNA families in maize showed expression differences >2-fold in the two lines, among which 14 members from four miRNA families were up-regulated and 14 members from 7 miRNA families were repressed in SSL-10. A genome wide degradome was sequenced to validate the miRNA target genes in solid experiment. In addition, novel miRNAs associated with ear development were predicted using a series of strict criteria, and 29 miRNAs representing eight families were predicted as novel miRNAs. Among the novel miRNAs, only one showed an expression difference >2-fold. The conserved and novel miRNAs with >2-fold expression differences were treated as candidate miRNAs involved in maize kernel row number determination. MiRNA-dependent gene expression regulation and physiological and morphological effects on ear development may explain why the SSSL changed kernel row number compared with its recurrent parent. Based on the interaction of miRNAs and their target genes, a possible miRNA-dependent pathway leading to the given DNA fragment inducing a change in kernel row number was proposed.
机译:为了检测参与确定玉米仁行数的微小RNA(miRNA),对中国玉米的优良自交系Zong3(行号14-16)和单节替代系(SSSL)SSL-10进行了下一代深度测序(第8-10行)来自相同的遗传背景。在SSL-10中,单个片段被插入分子标记bnlg1953和bnlg1811之间的1号染色体中。属于玉米中11个保守miRNA家族的28个miRNA在两系中表达差异> 2倍,其中四个miRNA家族的14个成员被上调,而7个miRNA家族的14个成员在SSL-10中被阻遏。对全基因组的降解组进行了测序,以验证固体实验中的miRNA靶基因。此外,使用一系列严格的标准预测了与耳朵发育相关的新型miRNA,并且代表八个家族的29种miRNA被预测为新型miRNA。在新型miRNA中,只有一种显示出表达差异> 2倍。具有> 2倍表达差异的保守和新颖的miRNA被视为参与玉米籽粒行数确定的候选miRNA。 MiRNA依赖的基因表达调控以及对耳朵发育的生理和形态学效应可能解释了为什么SSSL与轮回亲代相比改变了内核行数。基于miRNA及其靶基因的相互作用,提出了一种可能的miRNA依赖性途径,导致给定的DNA片段诱导仁行数发生变化。

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