Evaluation of leaf rust resistance in the Chinese wheat cultivar ‘Een1’

Wheat cultivar Een1, 34 near isogenic lines (NILs), and two cultivars were used as plant materials to evaluate the resistance of Een1 to leaf rust disease. Infection type identification and gene postulation were carried out by inoculation of 12 Chinese Puccinia triticina (Pt) pathotypes. Based on th...

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Main Authors: Na Zhang, Lina Zhao, Kahsay Tadesse Mawcha, Chenguang Zhao, Wenxiang Yang, Daqun Liu
Format: Article
Language:English
Published: PeerJ Inc. 2020-05-01
Series:PeerJ
Subjects:
Online Access:https://peerj.com/articles/8993.pdf
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author Na Zhang
Lina Zhao
Kahsay Tadesse Mawcha
Chenguang Zhao
Wenxiang Yang
Daqun Liu
author_facet Na Zhang
Lina Zhao
Kahsay Tadesse Mawcha
Chenguang Zhao
Wenxiang Yang
Daqun Liu
author_sort Na Zhang
collection DOAJ
description Wheat cultivar Een1, 34 near isogenic lines (NILs), and two cultivars were used as plant materials to evaluate the resistance of Een1 to leaf rust disease. Infection type identification and gene postulation were carried out by inoculation of 12 Chinese Puccinia triticina (Pt) pathotypes. Based on the unique phenotype of Een1, we speculated that Een1 might carry Lr gene(s) different from the tested ones. The chromosomal locations for resistance gene to leaf rust disease was employed using SSR primers mapping the populations derived from the cross between Een1 and susceptible Thatcher. A total of 285 plants in the F2 population were tested by inoculating Pt pathotype FHNQ during the seedling stage. Results from the segregation analysis fits a ratio of 3:1 ( ${\chi }_{3:1}^{2}=2.37$ χ 3 : 1 2 = 2 . 37 , P = 0.12), indicating the presence of a single dominant gene in Een1 conferring resistance to FHNQ. A total of 1,255 simple sequence repeat (SSR) primers were first used to identify the likely linked markers based on bulk segregation analysis (BSA), and then those likely linked markers were further genotyped in the F2 population for linkage analysis. Our linkage analysis found that the resistance gene (LrE1) was distal to seven SSR loci on the long arm of chromosome 7B, with distances from 2.6 cM (Xgwm344) to 27.1 cM (Xgwm131). The closest marker Xgwm344 was further verified with F3 lines.
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spelling doaj.art-4f71f73a6ef4408bac1ac13832a8979c2023-12-03T07:14:46ZengPeerJ Inc.PeerJ2167-83592020-05-018e899310.7717/peerj.8993Evaluation of leaf rust resistance in the Chinese wheat cultivar ‘Een1’Na Zhang0Lina Zhao1Kahsay Tadesse Mawcha2Chenguang Zhao3Wenxiang Yang4Daqun Liu5Technological Innovation Center for Biological Control of Crop Diseases and Insect Pests of Hebei Province, College of Plant Protection, Hebei Agricultrual University, Baoding, Hebei, ChinaTechnological Innovation Center for Biological Control of Crop Diseases and Insect Pests of Hebei Province, College of Plant Protection, Hebei Agricultrual University, Baoding, Hebei, ChinaDepartment of Plant Sciences, Aksum University Shire Campus, Shire, Tigray, EthiopiaTechnological Innovation Center for Biological Control of Crop Diseases and Insect Pests of Hebei Province, College of Plant Protection, Hebei Agricultrual University, Baoding, Hebei, ChinaTechnological Innovation Center for Biological Control of Crop Diseases and Insect Pests of Hebei Province, College of Plant Protection, Hebei Agricultrual University, Baoding, Hebei, ChinaGraduate School, Chinese Academy of Agricultural Sciences, Beijing, ChinaWheat cultivar Een1, 34 near isogenic lines (NILs), and two cultivars were used as plant materials to evaluate the resistance of Een1 to leaf rust disease. Infection type identification and gene postulation were carried out by inoculation of 12 Chinese Puccinia triticina (Pt) pathotypes. Based on the unique phenotype of Een1, we speculated that Een1 might carry Lr gene(s) different from the tested ones. The chromosomal locations for resistance gene to leaf rust disease was employed using SSR primers mapping the populations derived from the cross between Een1 and susceptible Thatcher. A total of 285 plants in the F2 population were tested by inoculating Pt pathotype FHNQ during the seedling stage. Results from the segregation analysis fits a ratio of 3:1 ( ${\chi }_{3:1}^{2}=2.37$ χ 3 : 1 2 = 2 . 37 , P = 0.12), indicating the presence of a single dominant gene in Een1 conferring resistance to FHNQ. A total of 1,255 simple sequence repeat (SSR) primers were first used to identify the likely linked markers based on bulk segregation analysis (BSA), and then those likely linked markers were further genotyped in the F2 population for linkage analysis. Our linkage analysis found that the resistance gene (LrE1) was distal to seven SSR loci on the long arm of chromosome 7B, with distances from 2.6 cM (Xgwm344) to 27.1 cM (Xgwm131). The closest marker Xgwm344 was further verified with F3 lines.https://peerj.com/articles/8993.pdfWheatLeaf rust diseaseLeaf rust resistance genePuccinia triticinaPolymorphismMolecular mapping
spellingShingle Na Zhang
Lina Zhao
Kahsay Tadesse Mawcha
Chenguang Zhao
Wenxiang Yang
Daqun Liu
Evaluation of leaf rust resistance in the Chinese wheat cultivar ‘Een1’
PeerJ
Wheat
Leaf rust disease
Leaf rust resistance gene
Puccinia triticina
Polymorphism
Molecular mapping
title Evaluation of leaf rust resistance in the Chinese wheat cultivar ‘Een1’
title_full Evaluation of leaf rust resistance in the Chinese wheat cultivar ‘Een1’
title_fullStr Evaluation of leaf rust resistance in the Chinese wheat cultivar ‘Een1’
title_full_unstemmed Evaluation of leaf rust resistance in the Chinese wheat cultivar ‘Een1’
title_short Evaluation of leaf rust resistance in the Chinese wheat cultivar ‘Een1’
title_sort evaluation of leaf rust resistance in the chinese wheat cultivar een1
topic Wheat
Leaf rust disease
Leaf rust resistance gene
Puccinia triticina
Polymorphism
Molecular mapping
url https://peerj.com/articles/8993.pdf
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