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Genome Instability in Solanum tuberosum Plants Regenerated from Protoplasts

机译:从原生质体再生的马铃薯马铃薯植株的基因组不稳定性

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摘要

Most examples of crop genome modification through transgene and genome editing involve the regeneration of whole plants from callus derived from explants or protoplasts. Interest in the latter has spiked because delivery of ribonucleoproteins (RNP) made of Cas9 and guide RNA can modify a genomic target without the use of transgenes. This can make regulatory approval less complicated. A drawback of this system, however, is somaclonal variation. Somaclonal variation is a syndrome entailing the appearance of novel and unexpected phenotypes in plants regenerated from callus in tissue culture. Historical cytological investigations of somaclonal variants reported frequent aneuploidy and possible chromosomal changes. Before applying the RNP editing technique in protoplasts, it is important to fully understand if and how genomic instability may result. We have established a protoplast regeneration platform in a tetraploid S. tuberosum variety, demonstrating strong genotype dependency in the efficiency of regeneration. To elucidate the impact of genome structural variation on this system, we analyzed 15 potato plants regenerated from protoplasts comparing them to 8 propagated cutting controls. Plant DNA was subject to Illumina sequencing and resulting mapped reads were counted by chromosomal bin providing dosage. Deviations from the expected four copies were evaluated by plotting the bin counts by chromosomes. All regenerated plants analyzed displayed some genome alteration regardless of whether their phenotype appeared normal or altered. In addition to aneuploidy, we also observed segmental deletion and duplications, chromothripsis-like changes and chimerism. All chromosomes could be affected but some displayed higher frequency of changes. This variation, observed by sequence-based chromosome dosage profiles, greatly exceeds what was originally anticipated, validating the importance of considering such analysis when generating plants from protoplasts, as can be done with gene editing via RNPs.
机译:通过转基因和基因组编辑进行农作物基因组修饰的大多数示例涉及从外植体或原生质体衍生的愈伤组织中再生整个植物。对后者的兴趣激增,是因为由Cas9制成的核糖核蛋白(RNP)和指导RNA的交付可以在不使用转基因的情况下修饰基因组靶标。这样可以减少监管审批的复杂性。但是,该系统的缺点是体细胞克隆变异。体细胞克隆变异是一种综合征,需要在组织培养中从愈伤组织再生的植物中出现新的和意外的表型。体细胞克隆变异的历史细胞学研究报道了频繁的非整倍性和可能的​​染色体变化。在原生质体中应用RNP编辑技术之前,重要的是要充分了解是否以及如何导致基因组不稳定。我们已经在四倍体马铃薯块茎品种中建立了原生质体再生平台,证明了再生效率中强大的基因型依赖性。为了阐明基因组结构变异对该系统的影响,我们分析了从原生质体再生的15种马铃薯植株,并将其与8种繁殖的cutting插对照进行了比较。将植物DNA进行Illumina测序,并通过提供剂量的染色体bin对得到的作图读数进行计数。通过按染色体标绘垃圾箱计数来评估与预期的四个副本的差异。分析的所有再生植物均显示出一些基因组改变,无论它们的表型是正常的还是已改变的。除非整倍性外,我们还观察到节段的缺失和重复,色杆菌样变化和嵌合。所有染色体都可能受到影响,但某些染色体显示出更高的变化频率。通过基于序列的染色体剂量分布观察到的这种变异大大超出了最初的预期,这证实了在通过原生质体生成植物时考虑进行此类分析的重要性,就像通过RNP进行基因编辑一样。

著录项

  • 作者

    Fossi, Michelle Margaret.;

  • 作者单位

    University of California, Davis.;

  • 授予单位 University of California, Davis.;
  • 学科 Genetics.;Cellular biology.;Developmental biology.
  • 学位 M.S.
  • 年度 2018
  • 页码 40 p.
  • 总页数 40
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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