Association between advanced generations and genealogy in inbred lines of snap bean by the Ward-Modified Location Model

Genetics of resistance to ascochyta blight was studied using different generations of fifteen crosses of chickpea (Cicer arietinum L.). Six parents comprising two susceptible varieties GL 769, C 214 and four resistant lines GG 1267, GL 90168, GL 96010 and GL 98010 were used to develop one S × S, eight S × R and six R × R crosses and some of the back crosses and F₃ generations were developed. Field screening technique was used to evaluate the different generations for disease reaction using mixture of ten prevalent isolates (ab₁–ab₁₀) of ascochyta blight (Ascochyta rabiei). Inheritance study showed digenic recessive control of resistance in the cross GL 769 × C 214, whereas monogenic recessive control of resistance was found in the crosses GL 769 × GL 98010 and C 214 × GL 98010. Digenic dominant and recessive control of resistance was found in the crosses GL 769 × GG 1267 and C 214 × GG 1267 while the crosses GL 769 × GL 90168 and C 214 × GL 96010 showed the monogenic dominant control of resistance. Trigenic dominant and recessive control of resistance was observed in the crosses GL 769 × GL 96010 and C 214 × GL 90168. Allelic relationship studies showed that three resistant parents viz., GG 1267, GL 96010 and GL 90168 possessed allelic single dominant gene for resistance. Besides, GG 1267 possessed two minor recessive genes for resistance, one of them was allelic to the minor recessive gene possessed by GL 90168 and other with GL 96010. The resistant parents GL 90168 and GL 96010 possessed non-allelic minor gene for resistance. The resistant parent GL 98010 possessed two minor recessive genes for resistance which were allelic to respective single recessive gene for resistance possessed by the susceptible parents GL 769 and C 214. The susceptible parents GL 769 and C 214 also possessed single independent inhibitory dominant susceptibility gene. The inhibitory gene was epistatic to the corresponding recessive gene for resistance.     

Inheritance of resistance to Fusarium wilt (race 2) in chickpea

The inheritance of resistance to Fusarium wilt (race 2) of chickpea was studied in a set of three crosses, i.e. ‘WR315’בC104’ (resistant × susceptible), ‘WR315’בK850’ (resistant × tolerant) and ‘K850’בGW5/7’ (tolerant × tolerant) in order to investigate the number of genes involved, their complementation and to find out whether resistant segregants are possible in a cross between two tolerant cultivars. Tests of F₁, F₂ and F₃ generations of these crosses under controlled conditions at ICRISAT, Patancheru, India, indicated involvement of three loci (two recessive and one dominant alleles). The homozygous recessive form at the first two loci conferred resistance whereas susceptibility occurred when the first two loci were in the dominant form. A dominant allele at the third locus can complement the dominant alleles at the other two loci to confer tolerance. Occurrence of resistant segregants in a cross between two tolerant cultivars was observed.     

Inheritance of stalk rot resistance in cauliflower (Brassica oleracea var. Botrytis L.)

Summary The inheritance of resistance in cauliflower to stalk rot (Sclerotinia sclerotiorum (Lib.) de Bary) was investigated in population from six generations of six crosses. Disease incidence was recorded on 4 parents, 6 F^s ₁, 6 F^s ₂ and 12 back-crosses in a screenhouse under artificially created epiphytotic conditions. Resistance to stalk rot in this set of parents was found to be polygenic and under the control of recessive genes and due primarily to additive gene action. A breeding strategy emphasizing recurrent selection should lead to improvement in resistance.     

Breeding for resistance to coffee berry disease in Coffea arabica L. II. Inheritance of the resistance

Summary The inheritance of resistance to coffee berry disease (CBD) has been studied by applying a preselection test to F₂ progenies of a half diallel cross between 11 coffee varieties with different degrees of resistance and to sets of parental, F₁, F₂, B₁₁ and B₁₂ generations of crosses between resistant and susceptible varieties. True resistance to CBD appears to be controlled by major genes on three different loci. The highly resistant variety Rume Sudan carries the dominant R- and the recessive K-genes. The non-allelic interaction between these two genes is of a duplicate nature. The R-locus has multiple alleles with R ₁R₁alleles present in Rume Sudan and the somewhat less effective R ₂R₂alleles in a variety like Pretoria, which also has the K-gene. The moderately resistant variety K7 carries only the recessive K-gene. The arabica-like variety Hibrido de Timor (a natural interspecific arabica x robusta hybrid) carries one gene for CBD resistance on the T-locus with intermediate gene action. It probably inherited this gene from its robusta parent. There is circumstantial evidence that the resistance to CBD is of a stable nature, but it is advisable to accumulate in one genotype as many resistance genes as possible by combining in the breeding programme the resistance of Rume Sudan with that of Hibrido de Timor.     

Inheritance and allelic relationship among gene(s) for blast resistance in pearl millet [Pennisetum glaucum (L.) R. Br.]

Six blast‐resistant pearl millet genotypes, ICMB 93333, ICMB 97222, ICMR 06444, ICMR 06222, ICMR 11003 and IP 21187‐P1, were crossed with two susceptible genotypes, ICMB 95444 and ICMB 89111 to generate F₁s, F₂s and backcrosses, BC₁P₁ (susceptible parent × F₁) and BC₁P₂ (resistant parent × F₁) for inheritance study. The resistant genotypes were crossed among themselves in half diallel to generate F₁s and F₂s for test of allelism. The F₁, F₂ and backcross generations, and their parents were screened in a glasshouse against Magnaporthe grisea isolates Pg 45 and Pg 53. The reaction of the F₁s, segregation pattern of F₂s and BC₁P₁ derived from crosses involving two susceptible parents and six resistant parents revealed the presence of single dominant gene governing resistance in the resistant genotypes. No segregation for blast reaction was observed in the F₂s derived from the crosses of resistant × resistant parents. The resistance reaction of these F₂s indicated that single dominant gene conferring resistance in the six genotypes is allelic, that is same gene imparts blast resistance in these genotypes to M. grisea isolates.     

Inheritance of resistance to Fusarium wilt and yield traits in pigeonpea

Fusarium wilt is the main pigeonpea production constraint in Malawi. The purpose of the study was to understand the nature and mechanism of inheritance of F. wilt resistance, yield and secondary traits in pigeonpea. 48 crosses were generated in a 12 lines × 4 testers mating scheme. Some F₁ plants were selfed for segregation analysis for inheritance pattern of resistance, while others were evaluated for resistance, yield and secondary traits. There were significant variations among F₁ plants for F. wilt, days to 50 % flowering, seed/pod, and number of secondary branches. Specific combining ability (SCA) effects were predominant for F. wilt, days to 50 % flowering and number of secondary branches. The general combining ability (GCA) effects, mainly due to maternal genotypes, were preponderant for yield and other secondary traits. The significance of GCA and SCA effects suggested that variations were due to additive gene action in both the testers and parental lines arising from their interactions, and the dominance effects due to interactions of the parental lines. The χ² analysis suggested dominant patterns of inheritance for wilt in most of the F₂ populations. The segregation ratios of 3:1, 15:1, and 9:7 suggested the involvement of single or two independent/complementary dominant genes in the test donors. Involvement of a few genes governing wilt resistance suggested the ease of breeding for this trait. Pedigree breeding method would be recommended for incorporating various traits in pigeonpea.     

Inheritance of resistance to cucumber green mottle mosaic virus in muskmelon (Cucumis melo L.)

Summary Studies on inheritance of resistance to CGMMV showed that resistance was governed by polygenes with recessive nature. Out of 15 crosses studied, 10 were found to be interacting. All the interacting crosses (except one Phoot x Harela) showed duplicate type of epistasis. Kachri x Phoot (R × R type) cross exhibited heterosis in F₁ and transgressive segregation in F₂ for resistance. Studies pointed out the need to exploit this F₁ further to develop a new breeding line with higher level of resistance than both the parents.     

Inheritance of stem termination in pigeon pea (Cajanus cajan (L.) Mill sp.)

Summary Inheritance studies on the stem termination in pigeon pea using F₁, F₂ and F₃ generations of two crosses between determinate and indeterminate lines suggested that two dominant genes with epistatic (inhibitory) interaction of one of them control the interminate growth habit. The gene symbols D. idid and ddIdId have been designated to the parental plants with determinate and indeterminate growth habits, respectively. The gene IdId was epistatic (inhibitory) to the gene D giving a ratio of 13 indeterminate: 3 determinate inthe F₂'s observed. F₃ segregation supported the proposed model on the mode of inheritance.     

Inheritance of race 1.2 Fusarium wilt resistance in four melon cultivars

The resistance to Fusarium oxysporum f.sp. melonis (Fom) race 1.2 has been studied in melons, such as the Portuguese accession ‘BG-5384’ and in the Japanese ‘Shiro Uri Okayama’, ‘Kogane Nashi Makuwa’, and ‘C-211’, since a good characterization of the resistance is necessary before its introgression into commercial varieties. These four melon accessions showed a high level of resistance to races 0, 1, and 2 of Fom, indicating that the partial resistance to the race 1.2 previously detected may not have been race specific. To determine the mode of inheritance of the resistance to Fom race 1.2, the F₁, F₂, BCP_R, and BCP_S generations from the crosses between the four resistant accessions above and ‘Piel de Sapo’, a Fom race 1.2 susceptible melon, were developed. They were subsequently inoculated with two Fom isolates, one from the pathotype 1.2Y and the other from the pathotype 1.2W. The area under the disease progress curve was determined for each inoculated plant, and the data were analyzed. We show that the resistance seen in these accessions is polygenically inherited with a complex genetic control because many epistatic interactions were detected. The three epistatic effects; additivity × additivity, dominance × dominance, and dominance × additivity are present and significant, with differing magnitudes from one cross to the next. The relatively low heritabilities, and these epistatic effects make difficult the improvement of the resistance, from these sources, through a standard selection procedure.     

Genetic analysis of resistance to <Emphasis Type="Italic">Fusarium</Emphasis> root rot in common bean

Fusarium root rot (FRR) is a major disease of common bean worldwide. Knowledge of the inheritance of resistance to FRR would be important in devising strategies to breed resistant varieties. Therefore, a 12 × 12 full diallel mating scheme with reciprocal crosses was performed to generate 132 F₁ progenies, which were then advanced to the F₃. The progenies were evaluated for resistance to FRR under green house conditions in Uganda. General combining ability (GCA) effects were highly significant (P ≤ 0.01) for disease scores. Specific combining ability effects were not significant (P > 0.05) in the F₁, but were highly significant (P < 0.01) in the F₃ generation. These results indicate that resistance to FRR was governed by genes with additive effects in combination with genes with non-additive effects. Reciprocal differences were also significant (P = 0.01) at F₁ and F₃, primarily reflecting a large influence of maternal effects in both these generations. In fact, susceptible parents did not differ significantly (P > 0.05) for disease scores when used as paternal parents in the F₃, but differed strongly as maternal parents (P = 0.0002). Generally, the progenies were distinctly more resistant when the resistant parent was used as the female in crosses, especially as observed in the F₃. The maternal effects were strong in the F₃ generation, suggesting a complex form of cytoplasmic–genetic interaction. The non-maternal reciprocal effects in the F₃ were significant (P < 0.05) in both the resistant × resistant diallel, and in the resistant × susceptible crosses. Mid-parent heterosis (MPH) occurred in most crosses, with average heterosis approximately equal in each of the three generations, indicating that epistasis was probably more influential than dominance of individual genes. Gene-number formulas indicated that several genes were involved in resistant × susceptible crosses. Among resistant × resistant crosses, many produced continuous distributions of F₁ progeny scores, suggesting polygenic inheritance, while bi-modal distributions were characteristic of the F₃ distributions, and fit expected ratios for two or three loci segregating in each cross. Dominant forms of epistasis favoring resistance were strongly indicated. Parent–offspring heritability estimates were moderate. Overall, the results indicate that resistant parents contain a number of different resistance genes that can be combined with the expectation of producing strong and durable resistance. The lines MLB-49-89A, MLB-48-89, RWR719 and Vuninkingi, with large and negative GCA effects, contributed high levels of resistance in crosses and would be recommended for use in breeding programs.     

Inheritance of resistance to Fusarium wilt in Indian lentil germplasm (Lens culinaris Medik.)

Summary Three lentil genotypes resistant to Fusarium oxysporum f.sp. lentis viz. Pant L 234, JL 446 and LP 286 were crossed with two susceptible ones. The hybrid plants were all resistant in the eight crosses evaluated. Segregation pattern for wilt reaction in F₂, BC(P₁), BC(P₂) and F₃ generations in field and glasshouse conditions indicated that resistance to Fusarium wilt is under the control of two dominant duplicate genes in Pant L 234 and two independent dominant genes with complementary effects in JL 446 and LP 286. A third dominant gene complementary to the dominant genes in JL 446 and LP 286 is present in two susceptible lines. Allelic tests suggest the presence of five independently segregating genes for resistance. Duplicate dominant genes in Pant L 234 are non-allelic to two dominant genes with complementary effects in LP 286 and JL 446 and the third gene complementary to the two genes in JL 446 and LP 286 in susceptible lines JL 641 and L 9–12. Gene symbols among parental genotypes have been designated.     

Inheritance of Cercospora Leaf Spot Resistance in Mung Bean, Vigna radiata (L.) Wilczek

Inheritance of Cercospora leaf spot resistance in mungbean was studied in 20 crosses involving crosses of resistant × susceptible, resistant × resistant, susceptible × susceptible lines. 3:1 ratio was observed in all 14 F₂s involving resistant × susceptible parents. The inheritance of Cercospora leaf spot resistance is thus controlled by a single recessive gene. Our results are contradictory to observations of Thaklk et al. (1977 a, b) who found monogenic dominant inheritance of Cercospora leaf spot resistance in mungbean.     

Combining ability analysis of Fusarium head blight resistance in western European wheat lines

The inheritance of Fusarium head blight (FHB) resistance was investigated in eight western European wheat lines using a half-diallel of F₁ crosses. The parents and F₁ crosses were point-inoculated, with a highly aggressive isolate of Fusarium graminearum, in replicated field and glasshouse trials. Type II resistance was assessed by measuring the % FHB spread and % wilted tips. There was a good correlation between the two disease parameters, % FHB spread area under the disease progress curve (AUDPC) and % wilted tips AUDPC (r = 0.86, P < 0.01). Correlation coefficients between the field and glasshouse environments were r = 0.46 (P < 0.01) for % FHB spread AUDPC and r = 0.40 (P < 0.05) for % wilted tips AUDPC. Both general combining ability (GCA) and specific combining ability (SCA) effects influenced the inheritance of FHB resistance, suggesting that in this set of parents both additive and non-additive (dominance or epistatic) effects influence the inheritance of type II FHB resistance. Highly significant GCA-by-environment (P < 0.0001) and SCA-by-environment (P < 0.005) interactions were also observed. Specific combinations of western European wheat varieties were identified with type II FHB resistance at a level equal to or more resistant than the winter wheat variety ‘Arina’.     

Inheritance of siliqua locule number and seed coat colour in Brassica juncea

The inheritance of siliqua locule number and seed coat colour in Brassica juncea was investigated, using three lines each of tetralocular brown seeded and bilocular yellow seeded. Three crosses of tetralocular brown seeded × bilocular yellow seeded lines were attempted and their F₁, F₂ and backcross generations were examined for segregation of these two traits. Brown seed colour and bilocular siliqua characters were found to be dominant over yellow seed and tetralocular siliqua, respectively. Chi‐square tests indicated that each trait is controlled by different sets of duplicate pairs of genes. Bilocular siliquae or brown seeds can result from the presence of either of two dominant alleles, whereas tetralocular siliquae or yellow seeds are produced when alleles at both loci are recessive. A joint segregation analysis of F₂ data indicated that the genes governing siliqua locule number and seed colour were inherited independently.     

Inheritance of Dry Root Rot (Rhizoctonia bataticola) Resistance in Chickpea (Cicer arietinum)

The inheritance of resistance to dry root rot of chickpea caused by Rhizoctonia bataticola was studied. Parental F₁ and F₂ populations of two resistant and two susceptible parents, along with 49 F₁ progenies of one of the resistant × susceptible crosses were rested for their reaction to dry root rot using the blotting-paper technique. All F, plants of the resistant × susceptible crosses were resistant; the F₂ generation fitted a 3 resistant: 1 susceptible ratio indicating monogenic inheritance, with resistance dominant over susceptibility. F³ family segregation data confirmed the results. No segregation occurred among the progeny of resistant × resistant and susceptible × susceptible crosses.     

Inheritance of resistance to the 'Kanpur' race of Phytophthora drechsleri in pigeonpea

Phytophthora drechsleri causes stem blight, which is one of the most serious diseases of pigeonpea. Eight races of this fungus have been identified, but the inheritance of resistance to all these races is not clear except for race P2. This study examined the inheritance of resistance to race ‘Kanpur’ (KPR) of P. drechsleri in eight crosses involving four resistant parents, viz.‘KPBR 80‐2‐1′, ‘KPBR 80‐2‐2′, ‘Hy 3C and ‘BDN 1′, and two susceptible parents, viz.‘Bahar’ and ‘PDA 10′. The reactions of the parental lines, and their F₁, F₂ and backcross generations were studied in an infected plot. In the F₁ generation of all crosses, a susceptible reaction was observed that indicated dominance of susceptibility over resistance. The segregation pattern in F₂ indicated that two homozygous recessive genes (pdr₁pdr₁pdr₂pdr₂) were responsible for imparting resistance in the parents, ‘KPBR 80‐2‐1’ and ‘KPBR 80‐2‐2′, and that a single homozygous recessive gene (pdrpdr) was responsible for resistance in the parents ‘Hy 3C and ‘BDN 1′. Therefore, ‘KPBR 80‐2‐1’ and ‘KPBR 80‐2‐2’ with two genes for resistance are better donors because the resistance transferred from them will be more durable compared with ‘Hy3C and ‘BDN1’ with only one gene for resistance.     

Inheritance of resistance to Verticillium wilt (Verticillium dahliae) in cotton (Gossypium hirsutum L.)

Verticillium wilt, caused by Verticillium dahliae Kleb., is a major constraint to cotton production in almost all countries where cotton is cultivated. Developing new cotton cultivars resistant to Verticillium wilt is the most effective and feasible way to combat the problem. Little is known about the inheritance of resistance to Verticillium wilt of cotton, especially that caused by the defoliating (D) and nondefoliating (ND) pathotypes of the soil‐borne fungus V. dahliae. The objective of this study was to determine the inheritance of resistance in cotton against both pathotypes of V. dahliae. Crosses were made between the susceptible parent ‘Cukurova 1518’ and each of four resistant parents PAUM 401, PAUM 403, PAUM 405 and PAUM 406 to produce F₂ generations in 2002 and F_2:3 families in 2003. Disease responses of parent and progeny populations to the D and ND pathotypes were scored based on a scale of 0‐4 (0, resistant; 4, susceptible). F₂ populations inoculated with the D pathotype showed a 3 : 1 (resistant : susceptible) plant segregation ratio. Tests of F_2:3 families confirmed that resistance was controlled by a single dominant gene. In contrast, analysis of data from F₂‐ and F₂‐derived F₃ families suggested that resistance to the ND pathotype is controlled by dominant alleles at two loci.     

Genetic analysis of resistance to watermelon bud necrosis orthotospovirus in watermelon [Citrullus lanatus (Thunb.) Matsum & Nakai]

An experiment was conducted to study the genetics and nature of gene action of resistance to watermelon bud necrosis orthotospovirus (WBNV) in watermelon. The experimental materials comprised of two resistant (BIL‐53 and IIHR‐19) and one susceptible (IIHR‐140) parents. Each of the resistant parents was crossed with the susceptible parent to develop six generations (P1, P2, F₁, F₂, BC1 and BC2) to study genetics. The results of segregation in F₂ and backcross progenies suggested that resistance is governed by a major dominant gene along with other background minor genes in both the crosses. BIL‐53 was found to possess higher degree of resistance with simple inheritance and hence may be of interest to breeders. Simple selection can be effective for improving the trait in the cross BIL‐53 × IIHR‐140 as additive gene action is prevalent.     

Identification and genetics of resistance to cercospora leaf spot (<Emphasis Type="Italic">Cercospora zonata</Emphasis>) in faba bean (<Emphasis Type="Italic">Vicia faba</Emphasis>)

The fungal disease cercospora leaf spot CLS (Cercospora zonata) has affected major faba bean (Vicia faba) production regions in southern Australian in the last several years. This study offers the first report of sources of resistance to CLS in faba bean and describes techniques to evaluate resistance to C. zonata in faba bean genotypes within a controlled environment. The method was rapid (43 days), repeatable (R ² > 0.74) and demonstrated positive correlations (R ² > 0.45–0.80) to data collected from field disease nurseries under naturally established CLS epiphytotics. All faba bean cultivars currently adopted by the Australian industry were found to be susceptible to CLS and defoliation was found to be an important component of disease expression. Genetic analysis of segregation patterns in F ₂ derived F ₃ families of 1322/2*Farah (resistant*susceptible) showed the mode of inheritance of resistance to C. zonata was monogenic dominant. F ₃ families were shown to segregate in the ratio of 1:2:1 for homozygous resistant: heterozygous: homozygous susceptible (χ₂² = 2.78; P > 0.05) and individual plants within heterozygous F ₃ families segregated in the ratio of 3:1 for resistant: susceptible responses (χ₁² = 2.93; P > 0.05). Monogenic dominant inheritance also explained the change in frequency of resistant and susceptible plants within a population of cv. Cairo following one generation of self-pollination (χ² = 0.88, 0.3 < P < 0.5). The sources of resistance identified in this study are being used to transfer CLS resistance to adapted faba bean genotypes for future cultivar releases to the southern Australian industry.     

Component analysis of duration from seeding to heading in rice by the basic vegetative phase and the photoperiod-sensitive phase

Summary Inheritance of the duration from seeding to heading in rice was analyzed by dividing the vegetative growth period into the basic vegetative phase (b.v.p.) and the photoperiod-sensitive phase (p.s.p.). Concurrent determination of the two physiologic phases on pure lines and hybrids was facilitated by testing vegetative tillers of the same plant under two photoperiods.In nine crosses of photoperiod-sensitive by insensitive arieties where the parents differed appreciably in b.v.p. estimates obtained under a 10-hour photoperiod, two to three Ef genes of relatively discrete effect controlled the F₂ variation in b.v.p. Short b.v.p. was controlled by dominant genes of cumulative but unequal effect. In three other sensitive × insensitive crosses where the parents differed less in b.v.p., the F₂ segregation could be ascribed to two to four pairs of metrical alleles with equal or unequal effect.Concurrent data obtained from sensitive × insensitive crosses grown under a 16-hour photoperiod indicate the action of one or two (duplicate) dominant Se genes in controlling strong sensitivity to a long photoperiod. One insensitive variety appeared to carry a recessive inhibitor, i-Se. The Se gene(s) is epistatic to the Ef genes in the expression of earliness under a short photoperiod. Pooled data also suggest an association between photoperiod sensitivity and a short b.v.p. in a large proportion of F₂ plants.Field data on the two principal components of the vegetative growth period obtained under natural daylength generally indicated agreement with duplicate plantings grown under controlled photoperiods. Segregation for the optimum photoperiod and critical photoperiod under a changing photoperiod in the field plantings probably resulted in modified expression of the Se and Ef genes.Research supported in part by grant GB-2417 from the U.S. National Science Foundation.