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A Collection of Mutants for CLE-Peptide-Encoding Genes in Arabidopsis Generated by CRISPR/Cas9-Mediated Gene Targeting

机译:通过CRISPR / CAS9介导的基因靶向产生的拟南芥Cle-肽编码基因的突变体的集合

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摘要

The ligand-receptor-mediated intercellular communication system plays important roles in coordinating developmental and physiological events in multicellular organisms. In plants, CLAVATA3/EMBRYO SURROUNDING REGION (CLE) peptides and their cognate receptors are thought to be involved in various aspects of the plant life cycle. Although the importance of this communication is broadly recognized, most CLE peptides are yet to be functionally characterized. A major problem in research on small signaling peptide-encoding genes is the limited number of loss-of-function mutants available due to their small gene size. CRISPR/Cas9-mediated gene targeting has the potential to overcome this problem, as it can be used to generate targeted mutations in essentially any gene, regardless of size. Here we generated a series of mutants of CLE-peptide-encoding genes. Newly generated clv3 and cle40 mutants reproduced the expected mutant phenotypes in the shoot apical meristem and root meristem, respectively. Our results show that CRISPR/Cas9-mediated gene targeting is a powerful tool for genetic analyses, even of small genes. We also report a novel mutant for CLE44 [which is thought to encode a tracheary elements differentiation inhibitory factor (TDIF)] and show that CLE44 contributes to vascular development. The bioresources presented here will be a powerful tool for further characterization of CLE peptides.
机译:配体 - 受体介导的细胞间通信系统在辅助多细胞生物中的发育和生理事件中起重要作用。在植物中,Clavata3 /胚胎周围区域(CLE)肽及其同源受体被认为参与植物生命周期的各个方面。尽管这种通信的重要性被广泛认识到,但大多数CLE肽尚未在功能上表征。小信号肽编码基因的研究中的一个主要问题是由于其小基因尺寸而可用的函数突变体损失有限。 CRISPR / CAS9介导的基因靶向具有克服该问题的可能性,因为它可以用于基本上任何基因产生靶向突变,无论尺寸如何。在这里,我们产生了一系列Cle-肽编码基因的突变体。新生成的CLV3和CLE40突变体分别在芽顶部分发和根系中复制了预期的突变表型。我们的研究结果表明,CRISPR / CAS9介导的基因靶向是遗传分析的强大工具,即使是小基因。我们还报告了CLE44的一种新型突变体[旨在编码气管性元素分化抑制因子(TDIF)]并表明CLE44有助于血管发育。这里提出的生物源是一种强大的工具,用于进一步表征Cle肽。

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