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Nicking Endonuclease-Mediated Vector Construction Strategies for Plant Gene Functional Research.
Gong, Qi; Wang, Bin; Lu, Xubiao; Tan, Jiantao; Hou, Yuke; Liu, Taoli; Liu, Yao-Guang; Zhu, Qinlong.
Afiliación
  • Gong Q; State Key Laboratory for Conservation and Utilization of Subtropical Agro-Bioresources, Guangzhou 510642, China.
  • Wang B; Guangdong Laboratory for Lingnan Modern Agriculture, Guangzhou 510642, China.
  • Lu X; College of Life Sciences, South China Agricultural University, Guangzhou 510642, China.
  • Tan J; State Key Laboratory for Conservation and Utilization of Subtropical Agro-Bioresources, Guangzhou 510642, China.
  • Hou Y; Guangdong Laboratory for Lingnan Modern Agriculture, Guangzhou 510642, China.
  • Liu T; College of Life Sciences, South China Agricultural University, Guangzhou 510642, China.
  • Liu YG; College of Life Sciences, South China Agricultural University, Guangzhou 510642, China.
  • Zhu Q; State Key Laboratory for Conservation and Utilization of Subtropical Agro-Bioresources, Guangzhou 510642, China.
Plants (Basel) ; 9(9)2020 Aug 25.
Article en En | MEDLINE | ID: mdl-32854250
Plant genetic engineering vectors, such as RNA interference (RNAi) and CRISPR/Cas9 vectors, are important tools for plant functional genomics. Efficient construction of these functional vectors can facilitate the study of gene function. Although some methods for vector construction have been reported, their operations are still complicated and costly. Here, we describe a simpler and low-cost vector construction method by nicking endonucleases-mediated DNA assembly (NEMDA), which uses nicking endonucleases to generate single-strand overhanging complementary ends for rapid assembly of DNA fragments into plasmids. Using this approach, we rapidly completed the construction of four RNAi vectors and a CRISPR/Cas9 knockout vector with five single-guide RNA (sgRNA)-expression cassettes for multiplex genome editing, and successfully achieved the goal of decreasing the expression of the target genes and knocking out the target genes at the same time in rice. These results indicate the great potential of NEMDA in assembling DNA fragments and constructing plasmids for molecular biology and functional genomics.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Plants (Basel) Año: 2020 Tipo del documento: Article País de afiliación: China Pais de publicación: Suiza

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Idioma: En Revista: Plants (Basel) Año: 2020 Tipo del documento: Article País de afiliación: China Pais de publicación: Suiza