4.7 Article

Morphogene-assisted transformation of Sorghum bicolor allows more efficient genome editing

期刊

PLANT BIOTECHNOLOGY JOURNAL
卷 20, 期 4, 页码 748-760

出版社

WILEY
DOI: 10.1111/pbi.13754

关键词

Sorghum; Agrobacterium; engineering; CRISPR; Cas9 editing; morphogene-assisted transformation; altruistic morphogene-assisted transformation

资金

  1. Department of Energy, Biological and Environmental Research Program [DE-SC0014081]
  2. DBT India
  3. IUSSTF
  4. US Cooperative Extension Service through the Division of Agriculture and Natural Resources of the University of California

向作者/读者索取更多资源

Sorghum bicolor is the fifth most important cereal worldwide and has multiple uses. Establishing gene function is crucial for improving sorghum and other important crop plants. New tools and methods have been developed to expedite research on gene function in this widely grown crop.
Sorghum bicolor (L.) Moench, the fifth most important cereal worldwide, is a multi-use crop for feed, food, forage and fuel. To enhance the sorghum and other important crop plants, establishing gene function is essential for their improvement. For sorghum, identifying genes associated with its notable abiotic stress tolerances requires a detailed molecular understanding of the genes associated with those traits. The limits of this knowledge became evident from our earlier in-depth sorghum transcriptome study showing that over 40% of its transcriptome had not been annotated. Here, we describe a full spectrum of tools to engineer, edit, annotate and characterize sorghum's genes. Efforts to develop those tools began with a morphogene-assisted transformation (MAT) method that led to accelerated transformation times, nearly half the time required with classical callus-based, non-MAT approaches. These efforts also led to expanded numbers of amenable genotypes, including several not previously transformed or historically recalcitrant. Another transformation advance, termed altruistic, involved introducing a gene of interest in a separate Agrobacterium strain from the one with morphogenes, leading to plants with the gene of interest but without morphogenes. The MAT approach was also successfully used to edit a target exemplary gene, phytoene desaturase. To identify single-copy transformed plants, we adapted a high-throughput technique and also developed a novel method to determine transgene independent integration. These efforts led to an efficient method to determine gene function, expediting research in numerous genotypes of this widely grown, multi-use crop.

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