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首页> 外文期刊>Journal of Agricultural Science >CRISPR/Cas9-Mediated Targeted Mutagenesis of Wild Soybean (Glycine soja) Hairy Roots Altered the Transcription Profile of the Mutant
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CRISPR/Cas9-Mediated Targeted Mutagenesis of Wild Soybean (Glycine soja) Hairy Roots Altered the Transcription Profile of the Mutant

机译:CRISPR / CAS9介导的野生大豆(甘氨酸SOJA)毛茸茸的诱变的靶向诱变改变了突变体的转录概况

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摘要

Clustered Regularly Interspaced Short Palindromic Repeat/CRISPR-associated protein 9 (CRISPR/Cas9) system has been regularly applied for genome editing and gene function identification in wild soybean (Glycine max) cultivars.However, till date no studies have demonstrated successful mutagenesis in wild soybean (Glycine soja) which is the ancestor of Glycine max and rich in stress tolerance genes.In the current study, we report the successful creation of mutations in the loci encoding plasma membrane Na+/H+ antiporter (SOS1) and nonselective cation channels (NSCC) in wild soybean hairy roots using the CRISPR/Cas9 system.Two genes, GsSOS1 and GsNSCC, were mutagenized with frequencies of 28.5% and 39.9%, respectively.Biallelic mutations in GsSOS1 were detected in transgenic hairy roots.GsSOS1 mutants exhibited altered Na+/K+ ratios in the roots under both control and salt-treated conditions.However, no significant effects of GsNSCC mutation on Na+/K+ ratios were observed.RNA-Seq analysis revealed that both GsSOS1 and GsNSCC mutation altered the transcription profiles in mutant roots.Many differentially expressed gene sets that are associated with various cellular functions were identified.Our results demonstrated that CRISPR/Cas9 systems as powerful tools for wild soybean genome editing and would significantly advance the gene mining and functional identification in wild soybean.
机译:聚集经常间隙的短语重复/ CRISPR相关蛋白质9(CRISPR / CAS9)系统已经定期用于野生大豆(甘氨酸最大)品种中的基因组编辑和基因功能鉴定。然而,迄今为止没有研究表明在野外成功诱变大豆(甘氨酸Soja)是甘氨酸最大和富含应力耐受基因的祖先。目前的研究中,我们报告了在编码血浆膜Na + / H +抗原剂(SOS1)和非选择性阳离子通道的基因座中的突变成功创造了(NSCC )在使用CRISPR / CAS9 System的野生大豆毛的根中。在GSSOS1和GSNSCC的频率下,分别被诱变为28.5%和39.9%。在转基因毛状罗辛中检测到GSSOS1中的裂纹突变。GSSOS1突变体表现出改变的Na + /在控制和盐处理条件下根部的K +比率。然而,观察到GSNSCC突变对Na + / K +比没有显着影响.RNA-SEQ分析显示GSSOS1和GSNSCC突变均改变了突变圈中的转录谱。鉴定了与各种蜂窝功能相关的差异表达的基因组。我们的结果表明CRISPR / CAS9系统作为野生大豆基因组编辑的强大工具,并将显着提高野生大豆基因采矿与功能鉴定。

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