scholarly journals Inheritance of er1-Based Broad-Spectrum Powdery Mildew Resistance in Pea (Pisum sativum L.)

2013 ◽  
Vol 41 (2) ◽  
pp. 485 ◽  
Author(s):  
Muhammad Abubakkar AZMAT ◽  
Asif Ali KHAN

The knowledge about the nature and number of gene(s) controlling resistance is the pre-requisite for the success of powdery mildew resistance breeding program in pea. Seven biparental cross combinations involving three highly resistant (It-96, No. 267 and JI 2302) and two highly susceptible (Climax and PF-400) pea genotypes were evaluated for their response to powdery mildew disease. The quantitative microscopic scale of disease assessment coupled with detached leaf assay was employed for the evaluation of disease response of the crosses and their generations (F1, F2, BCs, and BCr) against two highly virulent conidial isolates of Erysiphe pisi. The disease response of 677 F2 plants has revealed a typical monohybrid Mendelian 3 (susceptible): 1 (resistant) segregation, moreover, the evaluation of 254 BCr plants gave a perfect 1 (susceptible): 1(resistant) segregation. No complementation was observed among all the F1 plants of three complementation crosses, suggesting that the same allele (er-1) conditions complete and broad-spectrum resistance in all the powdery mildew resistant pea genotypes in homozygous recessive form.

2008 ◽  
Vol 21 (1) ◽  
pp. 30-39 ◽  
Author(s):  
Yuling Bai ◽  
Stefano Pavan ◽  
Zheng Zheng ◽  
Nana F. Zappel ◽  
Anja Reinstädler ◽  
...  

The resistant cherry tomato (Solanum lycopersicum var. cerasiforme) line LC-95, derived from an accession collected in Ecuador, harbors a natural allele (ol-2) that confers broad-spectrum and recessively inherited resistance to powdery mildew (Oidium neolycopersici). As both the genetic and phytopathological characteristics of ol-2–mediated resistance are reminiscent of powdery mildew immunity conferred by loss-of-function mlo alleles in barley and Arabidopsis, we initiated a candidate-gene approach to clone Ol-2. A tomato Mlo gene (SlMlo1) with high sequence-relatedness to barley Mlo and Arabidopsis AtMLO2 mapped to the chromosomal region harboring the Ol-2 locus. Complementation experiments using transgenic tomato lines as well as virus-induced gene silencing assays suggested that loss of SlMlo1 function is responsible for powdery mildew resistance conferred by ol-2. In progeny of a cross between a resistant line bearing ol-2 and the susceptible tomato cultivar Moneymaker, a 19-bp deletion disrupting the SlMlo1 coding region cosegregated with resistance. This polymorphism results in a frameshift and, thus, a truncated nonfunctional SlMlo1 protein. Our findings reveal the second example of a natural mlo mutant that possibly arose post-domestication, suggesting that natural mlo alleles might be evolutionarily short-lived due to fitness costs related to loss of mlo function.


Plant Disease ◽  
2021 ◽  
Author(s):  
Huanhuan Li ◽  
Xiubin Tian ◽  
Shaolong Pei ◽  
Wenqiang Men ◽  
Chao Ma ◽  
...  

Powdery mildew of wheat, caused by Blumeria graminis f. sp. tritici (Bgt), is a destructive disease of wheat. Cultivation of resistant varieties is the most cost-effective disease management strategy. Previous studies reported that chromosome 3Sl#2 present in Chinese Spring (CS)-Aegilops longissima 3Sl#2(3B) disomic substitution line TA3575 conferred resistance to powdery mildew. In this study, we further located the powdery mildew resistance gene(s) to the short arm of chromosome 3Sl#2 (3Sl#2S) by evaluating for Bgt-resistance of newly developed CS-Ae. longissima 3Sl#2 translocation lines. Meanwhile, TA7545, a previously designated CS-Ae. longissima 3Sl#3 disomic addition line, was re-identified as an isochromosome 3Sl#3S addition line and evaluated to confer resistance to powdery mildew, thus locating the resistance gene(s) to the short arm of chromosome 3Sl#3 (3Sl#3S). Based on transcriptome sequences of TA3575, ten novel chromosome 3SlS-specific markers were developed, of which, five could be used to distinguish between 3Sl#2S and 3Sl#3S derived from Ae. longissima accessions TL20 and TA1910 (TAM4), and the remaining five could identify both 3Sl#2S and 3Sl#3S. Besides, CL897, one of five markers specific to both 3Sl#2S and 3Sl#3S, could be used to detect Pm13 located at chromosome 3Sl#1S from Ae. longissima accession TL01 in diverse wheat genetic backgrounds. The powdery mildew resistance genes on chromosomes 3Sl#2S and 3Sl#3S, the CS-Ae. longissima 3Sl#2 translocation lines, and the 3SlS-specific markers developed in this study will provide new germplasm resources for powdery mildew resistance breeding and facilitate the transfer of Bgt-resistance genes into common wheat.


2018 ◽  
Vol 8 (1) ◽  
Author(s):  
Yuli Jin ◽  
Hongxing Xu ◽  
Pengtao Ma ◽  
Xiaoyi Fu ◽  
Liping Song ◽  
...  

2007 ◽  
pp. 275-283 ◽  
Author(s):  
L. Leus ◽  
J. Van Huylenbroeck ◽  
F. Rys ◽  
A. Dewitte ◽  
E. Van Bockstaele ◽  
...  

2011 ◽  
Vol 12 (9) ◽  
pp. 866-878 ◽  
Author(s):  
MATT HUMPHRY ◽  
ANJA REINSTÄDLER ◽  
SERGEY IVANOV ◽  
TON BISSELING ◽  
RALPH PANSTRUGA

Plant Disease ◽  
2021 ◽  
Author(s):  
Shulin Xue ◽  
Mingxue Lu ◽  
Shanshan Hu ◽  
Hongxing Xu ◽  
Yuyu Ma ◽  
...  

Powdery mildew, caused by fungal pathogen Blumeria graminis f. sp. tritici (Bgt), is one of agronomically important and widespread wheat diseases causing severe yield losses. Deployment of broad‐spectrum disease-resistance genes is the preferred strategy to prevent this pathogen. Chinese wheat landrace Honghuaxiaomai (HHXM) was resistant to all 23 tested Bgt isolates at the seedling stage. The F1, F2, and F2:3 progenies derived from the cross HHXM × Yangmai 158 were used in this study, and genetic analysis revealed that a single dominant gene, designated as PmHHXM, conferred resistance to Bgt isolate E09. Bulked segregant analysis and molecular mapping initially located PmHHXM to the distal region of chromosome 4AL. To fine map PmHHXM, two critical recombinants were identified from 592 F2 plants and delimited PmHHXM to a 0.18-cM Xkasp475200–Xhnu552 interval covering 1.77-Mb, in which a number of disease resistance-related gene clusters were annotated. Comparative mapping of this interval revealed a perturbed synteny among Triticeae species. This study reports the new powdery mildew resistance gene PmHHXM that seems different from three known QTL/genes identified on chromosome 4AL and has significant values for further genetic improvement. Analysis of the polymorphisms of 13 co-segregating markers between HHXM and 170 modern wheat cultivars indicates that Xhnu227 and Xsts478700 developed here are ideal for marker-assisted introgression of this resistance gene in wheat breeding.


Pathogens ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 25
Author(s):  
Qiang Zhang ◽  
Yinghui Li ◽  
Yiwen Li ◽  
Tzion Fahima ◽  
Qian-Hua Shen ◽  
...  

Powdery mildew, caused by the fungus Blumeria graminis f. sp. tritici (Bgt), has limited wheat yields in many major wheat-production areas across the world. Introducing resistance genes from wild relatives into cultivated wheat can enrich the genetic resources for disease resistance breeding. The powdery mildew resistance gene Pm60 was first identified in diploid wild wheat Triticum urartu (T. urartu). In this study, we used durum as a ‘bridge’ approach to transfer Pm60 and Pm60b into hexaploid common wheat. Synthetic hexaploid wheat (SHW, AABBAuAu), developed by crossing T. urartu (AuAu) with durum (AABB), was used for crossing and backcrossing with common wheat. The Pm60 alleles were tracked by molecular markers and the resistance to powdery mildew. From BC1F1 backcross populations, eight recombinant types were identified based on five Pm60-flanking markers, which indicated different sizes of the introgressed chromosome segments from T. urartu. Moreover, we have selected two resistance-harboring introgression lines with high self-fertility, which could be easily used in wheat breeding system. Our results showed that the durum was an excellent ‘bridge’ for introducing the target gene from diploid T. urartu into the hexaploid cultivated wheat. Moreover, these introgression lines could be deployed in wheat resistance breeding programs, together with the assistance of the molecular markers for Pm60 alleles.


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