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PARA: A New Platform for the Rapid Assembly of gRNA Arrays for Multiplexed CRISPR Technologies.

Guoliang YuanStanton MartinMd Mahmudul HassanGerald A TuskanXiaohan Yang
Published in: Cells (2022)
Multiplexed CRISPR technologies have great potential for pathway engineering and genome editing. However, their applications are constrained by complex, laborious and time-consuming cloning steps. In this research, we developed a novel method, PARA, which allows for the one-step assembly of multiple guide RNAs (gRNAs) into a CRISPR vector with up to 18 gRNAs. Here, we demonstrate that PARA is capable of the efficient assembly of transfer RNA/Csy4/ribozyme-based gRNA arrays. To aid in this process and to streamline vector construction, we developed a user-friendly PARAweb tool for designing PCR primers and component DNA parts and simulating assembled gRNA arrays and vector sequences.
Keyphrases
  • genome editing
  • crispr cas
  • high density
  • single cell
  • high throughput
  • genome wide
  • gene expression
  • single molecule
  • nucleic acid
  • risk assessment
  • dna methylation
  • climate change
  • low cost