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Related Concept Videos

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Recombinant DNA technology called transgenesis is often used to add a foreign gene or remove a detrimental gene from an organism. Such genetically modified organisms are called transgenic organisms.
The first-ever transgenic plant was a tobacco plant developed in 1983 that showed resistance against the tobacco mosaic virus. Since then, many transgenic plants have been developed and commercialized for improving the agricultural, ornamental, and horticultural value of a crop plant. Transgenic...
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Advancing plant gene activation with CRISPR-Act3.0.

Ali Movahedi1, Zhiying Mu2, Liming Yang2

  • 1State Key Laboratory of Tree Genetics and Breeding, College of Life Sciences, Nanjing Forestry University, Nanjing 210037, China; College of Arts and Sciences, Arlington International University, Wilmington, DE 19804, USA.

Trends in Biotechnology
|February 13, 2025
PubMed
Summary

We enhanced CRISPR-Act3.0 for plant gene activation, improving stability and consistency in complex polyploid genomes. This modified tool offers more reliable genetic engineering solutions for challenging plant research.

Keywords:
CRISPR-Act3.0CRISPRaCas12bGOLD-tracrRNASpRYgR2.0

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Area of Science:

  • Plant science
  • Genetics
  • Molecular biology

Background:

  • CRISPR-Act3.0 is a key tool for plant gene activation.
  • Challenges include structural instability and inconsistent activation in polyploid genomes.

Purpose of the Study:

  • To strategically modify CRISPR-Act3.0 for enhanced resilience and adaptability.
  • To improve gene activation precision in complex plant genomes.

Main Methods:

  • Strategic modifications to the CRISPR-Act3.0 system.
  • Testing in polyploid plant genomes.

Main Results:

  • Increased structural stability of the modified CRISPR-Act3.0.
  • More consistent and reliable gene activation observed.
  • Improved adaptability in complex plant genomes.

Conclusions:

  • The modified CRISPR-Act3.0 system shows significant improvements for plant genome engineering.
  • This enhanced tool addresses limitations of conventional methods in polyploid plants.