scholarly journals Identification and Molecular Mapping of a Wheat Gene for Resistance to an Unadapted Isolate of Colletotrichum cereale

2013 ◽  
Vol 103 (6) ◽  
pp. 575-582 ◽  
Author(s):  
Yoshihiro Inoue ◽  
Ryota Mori ◽  
Yujiro Takahashi ◽  
So Kiguchi ◽  
Takashi Enomoto ◽  
...  
Keyword(s):  
Molecular Mapping ◽  
Major Gene ◽  
Hypersensitive Reaction ◽  
Substitution Lines ◽  
Resistant Cultivars ◽  
Chromosome Substitution Lines ◽  
Colletotrichum Cereale ◽  
Wheat Gene ◽  
Genetic Mechanisms ◽  
Chromosome 5A

To elucidate genetic mechanisms of host species specificity between graminicolous anthracnose fungi and gramineous plants, infection assays were performed with a Sorghum isolate (Colletotrichum sublineolum), a Digitaria isolate (C. hanaui), a Polypogon isolate (C. cereale), and an Avena isolate (C. cereale). They were specifically virulent on the plants from which they were isolated. When 72 wheat lines were inoculated with an unadapted isolate from Asia Minor bluegrass (Cgp29), however, some exceptional cultivars were recognized. Although most cultivars were resistant to Cgp29, ‘Hope’ was susceptible. In F2 populations derived from crosses between three resistant cultivars—‘Norin 4’ (N4), ‘Chinese Spring’ (CS), and ‘Shin-chunaga’ (Sch)—and the susceptible Hope, resistant and susceptible seedlings segregated in a 3:1 ratio, suggesting that a major gene is involved in the resistance of each cultivar to Cgp29. In F2 populations derived from crosses between the three resistant cultivars, all seedlings were resistant, suggesting that these three cultivars carry the same gene. This resistance gene was designated as “resistance to Colletotrichum cereale 1” (Rcc1). Analysis with the CS–Hope chromosome substitution lines and molecular mapping revealed that Rcc1 was located on the long arm of chromosome 5A. Cytologically, Rcc1 was mainly associated with hypersensitive reaction. These results suggest that major genes similar to those controlling cultivar specificity are involved in the resistance of wheat against the unadapted isolate of C. cereale.

Identification of genes for resistance to a Digitaria isolate of Magnaporthe grisea in common wheat cultivars

Genome ◽  
2009 ◽  
Vol 52 (9) ◽  
pp. 801-809 ◽  
Author(s):  
N. T.T. Nga ◽  
V. T.B. Hau ◽  
Y. Tosa
Keyword(s):  
High Temperature ◽  
Common Wheat ◽  
Magnaporthe Grisea ◽  
Major Gene ◽  
Monosomic Analysis ◽  
Wheat Cultivars ◽  
Substitution Lines ◽  
Chromosome Substitution Lines ◽  
Blast Fungus ◽  
Specific Species

Common wheat cultivars are resistant to Magnaporthe grisea , a crabgrass ( Digitaria sanguinalis )-specific species of the blast fungus. To dissect the genetic basis of this “nonhost” type of resistance, we need an exceptional cultivar that is susceptible to M. grisea. A screening under various conditions revealed that Triticum aestivum ‘Chinese Spring’ (CS) was susceptible to M. grisea isolate Dig41 when incubated at high temperature (26 °C) after inoculation. By contrast, T. aestivum ‘P168’, ‘Shin-chunaga’ (Sch), ‘Norin 4’ (N4), ‘Norin 26’ (N26), ‘Norin 29’ (N29), ‘Red Egyptian’ (RE), and ‘Salmon’ (Slm) and Triticum compactum ‘No. 44’ (Cmp) were highly resistant even at the high temperature. When F2 seedlings derived from crosses between the resistant cultivars and CS were inoculated with Dig41, they segregated in a 3:1 ratio of resistant to susceptible, suggesting that the resistance of each cultivar is controlled by one major gene. Crosses of N4 with P168, Sch, N26, N29, and Cmp yielded no susceptible F2 seedlings, suggesting that these six cultivars share the same gene. Similarly, a cross between RE and Slm yielded no susceptible F2 seedlings, suggesting that these two cultivars share the same gene. On the other hand, crosses between the N4 group and the RE group produced resistant and susceptible seedlings in a 15:1 ratio, indicating that these two groups carry different genes inherited independently. The gene in N4 was located on chromosome 4A by a monosomic analysis and designated Rmg4, while the gene in RE was located on chromosome 6D using a series of chromosome substitution lines and designated Rmg5. These results suggest that the resistance of common wheat to M. grisea, an inappropriate species of the blast fungus, is under a simple genetic control.

The chromosomal locations in wheat of genes conferring differential response to the wild oat herbicide, difenzoquat

1987 ◽  
Vol 108 (3) ◽  
pp. 543-548 ◽  
Author(s):  
J. W. Snape ◽  
W. J. Angus ◽  
Beryl Parker ◽  
Debra Leckie
Keyword(s):  
Chinese Spring ◽  
Major Gene ◽  
Wheat Variety ◽  
Differential Response ◽  
Susceptible Variety ◽  
Monosomic Analysis ◽  
Wild Oat ◽  
Substitution Lines ◽  
Single Chromosome ◽  
Chromosome Substitution Lines

SummaryF2, monosomic analysis involving crosses between the monosomic series of a resistant wheat variety, Chinese Spring, and a susceptible variety, Sicco, has located a major gene locus, designated Dfql, on chromosome 2B of wheat which determines the differential response of these varieties to treatment with the wild oat herbicide, difenzoquat. The allele from Chinese Spring conferring resistance is dominant and studies of the responses of Chinese Spring single chromosome substitution lines and nullisomic–tetrasomic lines for chromosome 2B indicate that this allele actively promotes resistance to the herbicide. It is suggested that this gene may prevent inhibition of DNA synthesis in the apical meristem, which is the site of action of the herbicide (Pallett & Caseley, 1980).Other chromosomes were also implicated as carrying ‘modifier genes’ which affect the ratio of resistant: susceptible plants in F2 monosomic families, namely 1D, 2D, 3A, 3B, 5B and 5D. These chromosomes may affect the retention and translocation of the herbicide to the target site and hence the threshold of response.The simple inheritance of difenzoquat resistance indicates that it should be easy by conventional breeding techniques to transfer the resistance into susceptible varieties.

scholarly journals Effects of Interspecific Chromosome Substitution in Upland Cotton on Cottonseed Macronutrients

Plants ◽  
2021 ◽  
Vol 10 (6) ◽  
pp. 1158
Author(s):  
Nacer Bellaloui ◽  
Sukumar Saha ◽  
Jennifer L. Tonos ◽  
Jodi A. Scheffler ◽  
Johnie N. Jenkins ◽  
...  
Keyword(s):  
South Carolina ◽  
Upland Cotton ◽  
Field Experiments ◽  
Seed Quality ◽  
Recurrent Parent ◽  
Chromosome Substitution ◽  
Substitution Lines ◽  
Chromosome Substitution Lines ◽  
Macronutrient Content ◽  
Chromosome Arm

Nutrients, including macronutrients such as Ca, P, K, and Mg, are essential for crop production and seed quality, and for human and animal nutrition and health. Macronutrient deficiencies in soil lead to poor crop nutritional qualities and a low level of macronutrients in cottonseed meal-based products, leading to malnutrition. Therefore, the discovery of novel germplasm with a high level of macronutrients or significant variability in the macronutrient content of crop seeds is critical. To our knowledge, there is no information available on the effects of chromosome or chromosome arm substitution on cottonseed macronutrient content. The objective of this study was to evaluate the effects of chromosome or chromosome arm substitution on the variability and content of the cottonseed macronutrients Ca, K, Mg, N, P, and S in chromosome substitution lines (CS). Nine chromosome substitution lines were grown in two-field experiments at two locations in 2013 in South Carolina, USA, and in 2014 in Mississippi, USA. The controls used were TM-1, the recurrent parent of the CS line, and the cultivar AM UA48. The results showed major variability in macronutrients among CS lines and between CS lines and controls. For example, in South Carolina, the mean values showed that five CS lines (CS-T02, CS-T04, CS-T08sh, CS-B02, and CS-B04) had higher Ca level in seed than controls. Ca levels in these CS lines varied from 1.88 to 2.63 g kg−1 compared with 1.81 and 1.72 g kg−1 for TM-1 and AMUA48, respectively, with CS-T04 having the highest Ca concentration. CS-M08sh exhibited the highest K concentration (14.50 g kg−1), an increase of 29% and 49% over TM-1 and AM UA48, respectively. Other CS lines had higher Mg, P, and S than the controls. A similar trend was found at the MS location. This research demonstrated that chromosome substitution resulted in higher seed macronutrients in some CS lines, and these CS lines with a higher content of macronutrients can be used as a genetic tool towards the identification of desired seed nutrition traits. Also, the CS lines with higher desired macronutrients can be used as parents to breed for improved nutritional quality in Upland cotton, Gossypium hirsutum L., through improvement by the interspecific introgression of desired seed nutrient traits such as Ca, K, P, S, and N. The positive and significant (p ≤ 0.0001) correlation of P with Ca, P with Mg, S with P, and S with N will aid in understanding the relationships between nutrients to improve the fertilizer management program and maintain higher cottonseed nutrient content.

scholarly journals Genetic variation in the dietary sucrose modulation of enzyme activities in Drosophila melanogaster

1984 ◽  
Vol 43 (3) ◽  
pp. 307-321 ◽  
Author(s):  
Billy W. Geer ◽  
Cathy C. Laurie-Ahlberg
Keyword(s):  
Drosophila Melanogaster ◽  
Genetic Variation ◽  
Enzyme Activities ◽  
Glycogen Synthesis ◽  
Krebs Cycle ◽  
Natural Populations ◽  
Substitution Lines ◽  
Chromosome Substitution Lines ◽  
High Sucrose Diet ◽  
Selection Of

SUMMARYGenetic variation in the modulating effect of dietary sucrose was assessed in Drosophila melanogaster by examining 27 chromosome substitution lines coisogenic for the X and second chromosomes and possessing different third isogenic chromosomes derived from natural populations. An increase in the concentration of sucrose from 0·1% to 5% in modified Sang's medium C significantly altered the activities of 11 of 15 enzyme activities in third instar larvae, indicating that dietary sucrose modulates many, but not all, of the enzymes of D. melanogaster. A high sucrose diet promoted high activities of enzymes associated with lipid and glycogen synthesis and low activities of enzymes of the glycolytic and Krebs cycle pathways, reflecting the physiological requirements of the animal. Analyses of variance revealed significant genetic variation in the degrees to which sucrose modulated several enzyme activities. Analysis of correlations revealed some relationships between enzymes in the genetic effects on the modulation process. These observations suggest that adaptive evolutionary change may depend in part on the selection of enzyme activity modifiers that are distributed throughout the genome.

scholarly journals Identification of a Novel Locus Rmo2 Conditioning Resistance in Barley to Host-Specific Subgroups of Magnaporthe oryzae

2012 ◽  
Vol 102 (7) ◽  
pp. 674-682 ◽  
Author(s):  
Nguyen Thi Thanh Nga ◽  
Yoshihiro Inoue ◽  
Izumi Chuma ◽  
Gang-Su Hyon ◽  
Kazuma Okada ◽  
...  
Keyword(s):  
Magnaporthe Oryzae ◽  
Molecular Mapping ◽  
The Other ◽  
Avirulence Gene ◽  
Barley Cultivar ◽  
Avirulence Genes ◽  
Genetic Crosses ◽  
Barley Cultivars ◽  
Genetic Mechanisms ◽  
Common Parent

Barley cultivars show various patterns of resistance against isolates of Magnaporthe oryzae and M. grisea. Genetic mechanisms of the resistance of five representative barley cultivars were examined using a highly susceptible barley cultivar, ‘Nigrate’, as a common parent of genetic crosses. The resistance of the five cultivars against Setaria, Oryza, Eleusine, and Triticum isolates of M. oryzae was all attributed to a single locus, designated as Rmo2. Nevertheless, the Rmo2 locus in each cultivar was effective against a different range of isolates. Genetic analyses of pathogenicity suggested that each cultivar carries an allele at the Rmo2 locus that recognizes a different range of avirulence genes. One allele, Rmo2.a, corresponded to PWT1, which conditioned the avirulence of Setaria and Oryza isolates on wheat, in a gene-for-gene manner. The other alleles, Rmo2.b, Rmo2.c, and Rmo2.d, corresponded to more than one avirulence gene. On the other hand, the resistance of those cultivars to another species, M. grisea, was conditioned by another locus, designated as Rmo3. These results suggest that Rmo2 is effective against a broad range of blast isolates but is specific to M. oryzae. Molecular mapping revealed that Rmo2 is located on the 7H chromosome.

scholarly journals Identification and Molecular Mapping of a Gene Conferring Resistance to Pyrenophora tritici-repentis Race 3 in Tetraploid Wheat

2006 ◽  
Vol 96 (8) ◽  
pp. 885-889 ◽  
Author(s):  
P. K. Singh ◽  
J. L. Gonzalez-Hernandez ◽  
M. Mergoum ◽  
S. Ali ◽  
T. B. Adhikari ◽  
...  
Keyword(s):  
Resistance Genes ◽  
Molecular Mapping ◽  
Recombinant Inbred Lines ◽  
Tetraploid Wheat ◽  
Recessive Gene ◽  
Tan Spot ◽  
Substitution Lines ◽  
Disease Reaction ◽  
Pyrenophora Tritici Repentis ◽  
The Cross

Race 3 of the fungus Pyrenophora tritici-repentis, causal agent of tan spot, induces differential symptoms in tetraploid and hexaploid wheat, causing necrosis and chlorosis, respectively. This study was conducted to examine the genetic control of resistance to necrosis induced by P. tritici-repentis race 3 and to map resistance genes identified in tetraploid wheat (Triticum turgidum). A mapping population of recombinant inbred lines (RILs) was developed from a cross between the resistant genotype T. tur-gidum no. 283 (PI 352519) and the susceptible durum cv. Coulter. Based on the reactions of the Langdon-T. dicoccoides (LDN[DIC]) disomic substitution lines, chromosomal location of the resistance genes was determined and further molecular mapping of the resistance genes for race 3 was conducted in 80 RILs of the cross T. turgidum no. 283/Coulter. Plants were inoculated at the two-leaf stage and disease reaction was assessed 8 days after inoculation based on lesion type. Disease reaction of the LDN(DIC) lines and molecular mapping on the T. turgidum no. 283/Coulter population indicated that the gene, designated tsn2, conditioning resistance to race 3 is located on the long arm of chromosome 3B. Genetic analysis of the F2 generation and of the F4:5 and F6:7 families indicated that a single recessive gene controlled resistance to necrosis induced by race 3 in the cross studied.

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