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CRISPR-Cas9-mediated knockout of CYP79D1 and CYP79D2 in cassava attenuates toxic cyanogen production.
Gomez, Michael A; Berkoff, Kodiak C; Gill, Baljeet K; Iavarone, Anthony T; Lieberman, Samantha E; Ma, Jessica M; Schultink, Alex; Karavolias, Nicholas G; Wyman, Stacia K; Chauhan, Raj Deepika; Taylor, Nigel J; Staskawicz, Brian J; Cho, Myeong-Je; Rokhsar, Daniel S; Lyons, Jessica B.
Afiliação
  • Gomez MA; Innovative Genomics Institute, University of California, Berkeley, Berkeley, CA, United States.
  • Berkoff KC; Innovative Genomics Institute, University of California, Berkeley, Berkeley, CA, United States.
  • Gill BK; Department of Molecular & Cell Biology, University of California, Berkeley, Berkeley, CA, United States.
  • Iavarone AT; Innovative Genomics Institute, University of California, Berkeley, Berkeley, CA, United States.
  • Lieberman SE; California Institute for Quantitative Biosciences (QB3), University of California, Berkeley, Berkeley, CA, United States.
  • Ma JM; Innovative Genomics Institute, University of California, Berkeley, Berkeley, CA, United States.
  • Schultink A; Department of Plant & Microbial Biology, University of California, Berkeley, Berkeley, CA, United States.
  • Karavolias NG; Innovative Genomics Institute, University of California, Berkeley, Berkeley, CA, United States.
  • Wyman SK; Department of Plant & Microbial Biology, University of California, Berkeley, Berkeley, CA, United States.
  • Chauhan RD; Department of Plant & Microbial Biology, University of California, Berkeley, Berkeley, CA, United States.
  • Taylor NJ; Innovative Genomics Institute, University of California, Berkeley, Berkeley, CA, United States.
  • Staskawicz BJ; Department of Plant & Microbial Biology, University of California, Berkeley, Berkeley, CA, United States.
  • Cho MJ; Innovative Genomics Institute, University of California, Berkeley, Berkeley, CA, United States.
  • Rokhsar DS; Donald Danforth Plant Science Center, St. Louis, MO, United States.
  • Lyons JB; Donald Danforth Plant Science Center, St. Louis, MO, United States.
Front Plant Sci ; 13: 1079254, 2022.
Article em En | MEDLINE | ID: mdl-37007603
ABSTRACT
Cassava (Manihot esculenta) is a starchy root crop that supports over a billion people in tropical and subtropical regions of the world. This staple, however, produces the neurotoxin cyanide and requires processing for safe consumption. Excessive consumption of insufficiently processed cassava, in combination with protein-poor diets, can have neurodegenerative impacts. This problem is further exacerbated by drought conditions which increase this toxin in the plant. To reduce cyanide levels in cassava, we used CRISPR-mediated mutagenesis to disrupt the cytochrome P450 genes CYP79D1 and CYP79D2 whose protein products catalyze the first step in cyanogenic glucoside biosynthesis. Knockout of both genes eliminated cyanide in leaves and storage roots of cassava accession 60444; the West African, farmer-preferred cultivar TME 419; and the improved variety TMS 91/02324. Although knockout of CYP79D2 alone resulted in significant reduction of cyanide, mutagenesis of CYP79D1 did not, indicating these paralogs have diverged in their function. The congruence of results across accessions indicates that our approach could readily be extended to other preferred or improved cultivars. This work demonstrates cassava genome editing for enhanced food safety and reduced processing burden, against the backdrop of a changing climate.
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Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Idioma: En Ano de publicação: 2022 Tipo de documento: Article