Segregation analysis for bacterial leaf blight disease resistance genes in rice ‘MR219’ using SSR marker
ABSTRACT Bacterial leaf blight (BLB) caused by Xanthomonas oryzae pv. oryzae is one of the major hindrances in rice (Oryza sativa L.) production across the world including Malaysia. Therefore, the development of disease-resistant varieties remains a very economical and effective method of controllin...
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Instituto de Investigaciones Agropecuarias, INIA
2020
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oai:scielo:S0718-583920200002002272020-11-30Segregation analysis for bacterial leaf blight disease resistance genes in rice ‘MR219’ using SSR markerZuki,Zakiah MohdRafii,Mohd Y.Ramli,AsfalizaOladosu,YusuffLatif,Mohammad AbdulSijam,KamaruzamanIsmail,Mohd RaziSarif,Hamidah Mohd Disease resistance F2 bulk population Oryza sativa rice bacterial leaf blight simple sequence repeat ABSTRACT Bacterial leaf blight (BLB) caused by Xanthomonas oryzae pv. oryzae is one of the major hindrances in rice (Oryza sativa L.) production across the world including Malaysia. Therefore, the development of disease-resistant varieties remains a very economical and effective method of controlling BLB in rice. Based on this background, this study was conducted to analyze segregation pattern of simple-sequence repeat (SSR) markers associated with BLB resistance genes in an F2 bulk population derived from a resistant variety (IRBB60) and a susceptible variety (MR219). Out of 129 simple sequence repeat (SSR) markers screened, 18 distinct polymorphism markers including R-gene based markers were used to screen 345 F2 progenies for resistance to BLB. Among the polymorphic markers, the chi-square analyses showed that 15 SSR markers (i.e. RM13 (xa5), RM21 (Xa21), RM122 (xa5), RM153 (xa5), RM164 (Xa13), RM206 (Xa10), RM5509, RM20B, RM25, RM163, RM169, RM218, RM267, RM276, and RM334) had a segregation ratio of 1:2:1 for a single gene model (df = 2.0, p ≤ 0.05). For phenotypic ratio, the F2 population segregated in ratio 3:1 (R:S) for resistant and susceptible plants, respectively. This indicated that resistance to BLB caused by pathotype X. oryzae pv. oryzae (Xoo) in the ‘MR219’ × ‘IRBB60’ F2 population is controlled by single dominant genes. The result presented in this study will help breeders to further breeding research in rice by enabling selection based on the genotype rather than on the phenotype. Similarly, the markers reported in this study will serve as a valuable tool for marker-aided selection for BLB resistance gene.info:eu-repo/semantics/openAccessInstituto de Investigaciones Agropecuarias, INIAChilean journal of agricultural research v.80 n.2 20202020-06-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0718-58392020000200227en10.4067/S0718-58392020000200227 |
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language |
English |
topic |
Disease resistance F2 bulk population Oryza sativa rice bacterial leaf blight simple sequence repeat |
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Disease resistance F2 bulk population Oryza sativa rice bacterial leaf blight simple sequence repeat Zuki,Zakiah Mohd Rafii,Mohd Y. Ramli,Asfaliza Oladosu,Yusuff Latif,Mohammad Abdul Sijam,Kamaruzaman Ismail,Mohd Razi Sarif,Hamidah Mohd Segregation analysis for bacterial leaf blight disease resistance genes in rice ‘MR219’ using SSR marker |
description |
ABSTRACT Bacterial leaf blight (BLB) caused by Xanthomonas oryzae pv. oryzae is one of the major hindrances in rice (Oryza sativa L.) production across the world including Malaysia. Therefore, the development of disease-resistant varieties remains a very economical and effective method of controlling BLB in rice. Based on this background, this study was conducted to analyze segregation pattern of simple-sequence repeat (SSR) markers associated with BLB resistance genes in an F2 bulk population derived from a resistant variety (IRBB60) and a susceptible variety (MR219). Out of 129 simple sequence repeat (SSR) markers screened, 18 distinct polymorphism markers including R-gene based markers were used to screen 345 F2 progenies for resistance to BLB. Among the polymorphic markers, the chi-square analyses showed that 15 SSR markers (i.e. RM13 (xa5), RM21 (Xa21), RM122 (xa5), RM153 (xa5), RM164 (Xa13), RM206 (Xa10), RM5509, RM20B, RM25, RM163, RM169, RM218, RM267, RM276, and RM334) had a segregation ratio of 1:2:1 for a single gene model (df = 2.0, p ≤ 0.05). For phenotypic ratio, the F2 population segregated in ratio 3:1 (R:S) for resistant and susceptible plants, respectively. This indicated that resistance to BLB caused by pathotype X. oryzae pv. oryzae (Xoo) in the ‘MR219’ × ‘IRBB60’ F2 population is controlled by single dominant genes. The result presented in this study will help breeders to further breeding research in rice by enabling selection based on the genotype rather than on the phenotype. Similarly, the markers reported in this study will serve as a valuable tool for marker-aided selection for BLB resistance gene. |
author |
Zuki,Zakiah Mohd Rafii,Mohd Y. Ramli,Asfaliza Oladosu,Yusuff Latif,Mohammad Abdul Sijam,Kamaruzaman Ismail,Mohd Razi Sarif,Hamidah Mohd |
author_facet |
Zuki,Zakiah Mohd Rafii,Mohd Y. Ramli,Asfaliza Oladosu,Yusuff Latif,Mohammad Abdul Sijam,Kamaruzaman Ismail,Mohd Razi Sarif,Hamidah Mohd |
author_sort |
Zuki,Zakiah Mohd |
title |
Segregation analysis for bacterial leaf blight disease resistance genes in rice ‘MR219’ using SSR marker |
title_short |
Segregation analysis for bacterial leaf blight disease resistance genes in rice ‘MR219’ using SSR marker |
title_full |
Segregation analysis for bacterial leaf blight disease resistance genes in rice ‘MR219’ using SSR marker |
title_fullStr |
Segregation analysis for bacterial leaf blight disease resistance genes in rice ‘MR219’ using SSR marker |
title_full_unstemmed |
Segregation analysis for bacterial leaf blight disease resistance genes in rice ‘MR219’ using SSR marker |
title_sort |
segregation analysis for bacterial leaf blight disease resistance genes in rice ‘mr219’ using ssr marker |
publisher |
Instituto de Investigaciones Agropecuarias, INIA |
publishDate |
2020 |
url |
http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0718-58392020000200227 |
work_keys_str_mv |
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