Cargando…

CRISPR/Cas9‐mediated tetra‐allelic mutation of the ‘Green Revolution’ SEMIDWARF‐1 (SD‐1) gene confers lodging resistance in tef (Eragrostis tef)

Tef is a staple food and a valuable cash crop for millions of people in Ethiopia. Lodging is a major limitation to tef production, and for decades, the development of lodging resistant varieties proved difficult with conventional breeding approaches. We used CRISPR/Cas9 to introduce knockout mutatio...

Descripción completa

Detalles Bibliográficos
Autores principales: Beyene, Getu, Chauhan, Raj Deepika, Villmer, Justin, Husic, Nada, Wang, Ning, Gebre, Endale, Girma, Dejene, Chanyalew, Solomon, Assefa, Kebebew, Tabor, Girma, Gehan, Malia, McGrone, Michael, Yang, Meizhu, Lenderts, Brian, Schwartz, Chris, Gao, Huirong, Gordon‐Kamm, William, Taylor, Nigel J., MacKenzie, Donald J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9398311/
https://www.ncbi.nlm.nih.gov/pubmed/35560779
http://dx.doi.org/10.1111/pbi.13842
_version_ 1784772303810199552
author Beyene, Getu
Chauhan, Raj Deepika
Villmer, Justin
Husic, Nada
Wang, Ning
Gebre, Endale
Girma, Dejene
Chanyalew, Solomon
Assefa, Kebebew
Tabor, Girma
Gehan, Malia
McGrone, Michael
Yang, Meizhu
Lenderts, Brian
Schwartz, Chris
Gao, Huirong
Gordon‐Kamm, William
Taylor, Nigel J.
MacKenzie, Donald J.
author_facet Beyene, Getu
Chauhan, Raj Deepika
Villmer, Justin
Husic, Nada
Wang, Ning
Gebre, Endale
Girma, Dejene
Chanyalew, Solomon
Assefa, Kebebew
Tabor, Girma
Gehan, Malia
McGrone, Michael
Yang, Meizhu
Lenderts, Brian
Schwartz, Chris
Gao, Huirong
Gordon‐Kamm, William
Taylor, Nigel J.
MacKenzie, Donald J.
author_sort Beyene, Getu
collection PubMed
description Tef is a staple food and a valuable cash crop for millions of people in Ethiopia. Lodging is a major limitation to tef production, and for decades, the development of lodging resistant varieties proved difficult with conventional breeding approaches. We used CRISPR/Cas9 to introduce knockout mutations in the tef orthologue of the rice SEMIDWARF‐1 (SD‐1) gene to confer semidwarfism and ultimately lodging resistance. High frequency recovery of transgenic and SD‐1 edited tef lines was achieved in two tef cultivars by Agrobacterium‐mediated delivery into young leaf explants of gene editing reagents along with transformation and regeneration enhancing morphogenic genes, BABY BOOM (BBM) and WUSCHEL2 (WUS2). All of the 23 lines analyzed by next‐generation sequencing had at least two or more alleles of SD‐1 mutated. Of these, 83% had tetra‐allelic frameshift mutations in the SD‐1 gene in primary tef regenerants, which were inherited in subsequent generations. Phenotypic data generated on T(1) and T(2) generations revealed that the sd‐1 lines have reduced culm and internode lengths with no reduction in either panicle or peduncle lengths. These characteristics are comparable with rice sd‐1 plants. Measurements of lodging, in greenhouse‐grown plants, showed that sd‐1 lines have significantly higher resistance to lodging at the heading stage compared with the controls. This is the first demonstration of the feasibility of high frequency genetic transformation and CRISPR/Cas9‐mediated genome editing in this highly valuable but neglected crop. The findings reported here highlight the potential of genome editing for the improvement of lodging resistance and other important traits in tef.
format Online
Article
Text
id pubmed-9398311
institution National Center for Biotechnology Information
language English
publishDate 2022
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-93983112022-08-26 CRISPR/Cas9‐mediated tetra‐allelic mutation of the ‘Green Revolution’ SEMIDWARF‐1 (SD‐1) gene confers lodging resistance in tef (Eragrostis tef) Beyene, Getu Chauhan, Raj Deepika Villmer, Justin Husic, Nada Wang, Ning Gebre, Endale Girma, Dejene Chanyalew, Solomon Assefa, Kebebew Tabor, Girma Gehan, Malia McGrone, Michael Yang, Meizhu Lenderts, Brian Schwartz, Chris Gao, Huirong Gordon‐Kamm, William Taylor, Nigel J. MacKenzie, Donald J. Plant Biotechnol J Research Articles Tef is a staple food and a valuable cash crop for millions of people in Ethiopia. Lodging is a major limitation to tef production, and for decades, the development of lodging resistant varieties proved difficult with conventional breeding approaches. We used CRISPR/Cas9 to introduce knockout mutations in the tef orthologue of the rice SEMIDWARF‐1 (SD‐1) gene to confer semidwarfism and ultimately lodging resistance. High frequency recovery of transgenic and SD‐1 edited tef lines was achieved in two tef cultivars by Agrobacterium‐mediated delivery into young leaf explants of gene editing reagents along with transformation and regeneration enhancing morphogenic genes, BABY BOOM (BBM) and WUSCHEL2 (WUS2). All of the 23 lines analyzed by next‐generation sequencing had at least two or more alleles of SD‐1 mutated. Of these, 83% had tetra‐allelic frameshift mutations in the SD‐1 gene in primary tef regenerants, which were inherited in subsequent generations. Phenotypic data generated on T(1) and T(2) generations revealed that the sd‐1 lines have reduced culm and internode lengths with no reduction in either panicle or peduncle lengths. These characteristics are comparable with rice sd‐1 plants. Measurements of lodging, in greenhouse‐grown plants, showed that sd‐1 lines have significantly higher resistance to lodging at the heading stage compared with the controls. This is the first demonstration of the feasibility of high frequency genetic transformation and CRISPR/Cas9‐mediated genome editing in this highly valuable but neglected crop. The findings reported here highlight the potential of genome editing for the improvement of lodging resistance and other important traits in tef. John Wiley and Sons Inc. 2022-06-10 2022-09 /pmc/articles/PMC9398311/ /pubmed/35560779 http://dx.doi.org/10.1111/pbi.13842 Text en © 2022 The Authors. Plant Biotechnology Journal published by Society for Experimental Biology and The Association of Applied Biologists and John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Articles
Beyene, Getu
Chauhan, Raj Deepika
Villmer, Justin
Husic, Nada
Wang, Ning
Gebre, Endale
Girma, Dejene
Chanyalew, Solomon
Assefa, Kebebew
Tabor, Girma
Gehan, Malia
McGrone, Michael
Yang, Meizhu
Lenderts, Brian
Schwartz, Chris
Gao, Huirong
Gordon‐Kamm, William
Taylor, Nigel J.
MacKenzie, Donald J.
CRISPR/Cas9‐mediated tetra‐allelic mutation of the ‘Green Revolution’ SEMIDWARF‐1 (SD‐1) gene confers lodging resistance in tef (Eragrostis tef)
title CRISPR/Cas9‐mediated tetra‐allelic mutation of the ‘Green Revolution’ SEMIDWARF‐1 (SD‐1) gene confers lodging resistance in tef (Eragrostis tef)
title_full CRISPR/Cas9‐mediated tetra‐allelic mutation of the ‘Green Revolution’ SEMIDWARF‐1 (SD‐1) gene confers lodging resistance in tef (Eragrostis tef)
title_fullStr CRISPR/Cas9‐mediated tetra‐allelic mutation of the ‘Green Revolution’ SEMIDWARF‐1 (SD‐1) gene confers lodging resistance in tef (Eragrostis tef)
title_full_unstemmed CRISPR/Cas9‐mediated tetra‐allelic mutation of the ‘Green Revolution’ SEMIDWARF‐1 (SD‐1) gene confers lodging resistance in tef (Eragrostis tef)
title_short CRISPR/Cas9‐mediated tetra‐allelic mutation of the ‘Green Revolution’ SEMIDWARF‐1 (SD‐1) gene confers lodging resistance in tef (Eragrostis tef)
title_sort crispr/cas9‐mediated tetra‐allelic mutation of the ‘green revolution’ semidwarf‐1 (sd‐1) gene confers lodging resistance in tef (eragrostis tef)
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9398311/
https://www.ncbi.nlm.nih.gov/pubmed/35560779
http://dx.doi.org/10.1111/pbi.13842
work_keys_str_mv AT beyenegetu crisprcas9mediatedtetraallelicmutationofthegreenrevolutionsemidwarf1sd1geneconferslodgingresistanceinteferagrostistef
AT chauhanrajdeepika crisprcas9mediatedtetraallelicmutationofthegreenrevolutionsemidwarf1sd1geneconferslodgingresistanceinteferagrostistef
AT villmerjustin crisprcas9mediatedtetraallelicmutationofthegreenrevolutionsemidwarf1sd1geneconferslodgingresistanceinteferagrostistef
AT husicnada crisprcas9mediatedtetraallelicmutationofthegreenrevolutionsemidwarf1sd1geneconferslodgingresistanceinteferagrostistef
AT wangning crisprcas9mediatedtetraallelicmutationofthegreenrevolutionsemidwarf1sd1geneconferslodgingresistanceinteferagrostistef
AT gebreendale crisprcas9mediatedtetraallelicmutationofthegreenrevolutionsemidwarf1sd1geneconferslodgingresistanceinteferagrostistef
AT girmadejene crisprcas9mediatedtetraallelicmutationofthegreenrevolutionsemidwarf1sd1geneconferslodgingresistanceinteferagrostistef
AT chanyalewsolomon crisprcas9mediatedtetraallelicmutationofthegreenrevolutionsemidwarf1sd1geneconferslodgingresistanceinteferagrostistef
AT assefakebebew crisprcas9mediatedtetraallelicmutationofthegreenrevolutionsemidwarf1sd1geneconferslodgingresistanceinteferagrostistef
AT taborgirma crisprcas9mediatedtetraallelicmutationofthegreenrevolutionsemidwarf1sd1geneconferslodgingresistanceinteferagrostistef
AT gehanmalia crisprcas9mediatedtetraallelicmutationofthegreenrevolutionsemidwarf1sd1geneconferslodgingresistanceinteferagrostistef
AT mcgronemichael crisprcas9mediatedtetraallelicmutationofthegreenrevolutionsemidwarf1sd1geneconferslodgingresistanceinteferagrostistef
AT yangmeizhu crisprcas9mediatedtetraallelicmutationofthegreenrevolutionsemidwarf1sd1geneconferslodgingresistanceinteferagrostistef
AT lendertsbrian crisprcas9mediatedtetraallelicmutationofthegreenrevolutionsemidwarf1sd1geneconferslodgingresistanceinteferagrostistef
AT schwartzchris crisprcas9mediatedtetraallelicmutationofthegreenrevolutionsemidwarf1sd1geneconferslodgingresistanceinteferagrostistef
AT gaohuirong crisprcas9mediatedtetraallelicmutationofthegreenrevolutionsemidwarf1sd1geneconferslodgingresistanceinteferagrostistef
AT gordonkammwilliam crisprcas9mediatedtetraallelicmutationofthegreenrevolutionsemidwarf1sd1geneconferslodgingresistanceinteferagrostistef
AT taylornigelj crisprcas9mediatedtetraallelicmutationofthegreenrevolutionsemidwarf1sd1geneconferslodgingresistanceinteferagrostistef
AT mackenziedonaldj crisprcas9mediatedtetraallelicmutationofthegreenrevolutionsemidwarf1sd1geneconferslodgingresistanceinteferagrostistef