Genetics of spike length in durum wheat

Gene effects were analyzed using mean spike length of 12 populations, viz., both parents, F₁, F₂, first back cross generation, BC₁ and BC₂, second backcross generations, BC₁₁,BC₁₂, BC₂₁ and BC₂₂ along with BC₁ self and BC₂ self derived by selfing BC₁ and BC₂populations of three crosses involving six diverse cultivars of Triticum durumto determine the nature of gene actions governing spike length through generation mean analysis under normal and late sown environments. The six-parameter model was adequate in most of the cases to explain genetic variation among the generation means under both the sowing environments. Additive (d) gene effect was significant in all the cases, whereas dominance (h) gene effect was not so frequently observed significant. Epistatic effects, particularly digenic types were predominant over additive and dominance effects in most of the cases under both normal and late sown environments except in the cross Cocorit 71 × A-9-30-1 (normal sown).Additive × dominance × dominance (y), trigenic interaction played significant role in controlling the inheritance of this trait in the cross HI 8062 × JNK-4W-128under late sown condition. Duplicate epistasis was observed in the cross HI 8062× JNK-4W-128 (normal sown). Non-fixable gene effects were of higher magnitude than fixable gene effects in almost all cases, confirmed the major role of non-additive gene effects to control the inheritance of spike length in durum wheat. Significant heterosis over better parent was not observed. Similarly, inbreeding depression was not commonly observed. Favourable and suitable environment must be considered before finalizing breeding programme for its simple inheritance to get desirable improvement for high grain yield. Hybridization systems, such as biparental mating and / or diallel selective mating, which exploit both additive and non-additive gene effects, simultaneously, could be useful in the improvement of spike length in durum wheat. This revised version was published online in July 2006 with corrections to the Cover Date.     

Genetic studies for seed size and grain yield traits in kabuli chickpea

Seed size, determined by 100-seed weight, is an important yield component and trade value trait in kabuli chickpea. In the present investigation, the small seeded kabuli genotype ICC 16644 was crossed with four genotypes (JGK 2, KAK 2, KRIPA and ICC 17109) and F₁, F₂ and F₃ populations were developed to study the gene action involved in seed size and other yield attributing traits. Scaling test and joint scaling test revealed the presence of epistasis for days to first flower, days to maturity, plant height, number of pods per plant, number of seeds per plant, number of seeds per pod, biological yield per plant, grain yield per plant and 100-seed weight. Additive, additive?×?additive and dominance?×?dominance effects were found to govern days to first flower. Days to maturity and plant height were under the control of both the main as well as interaction effects. Number of seeds per pod was predominantly under the control of additive and additive?×?additive effects. For grain yield per plant, additive and dominance?×?dominance effects were significant in the cross ICC 16644?×?KAK 2, whereas, additive?×?additive effects were important in the cross ICC 16644?×?JGK 2. Additive, dominance and epistatic effects influenced seed size. The study emphasized the existence of duplicate epistasis for most of the traits. To explore both additive and non-additive gene actions for phenological traits and yield traits, selection in later generations would be more effective.     

Combining ability analysis and association of yield and yield components among selected cowpea lines

The study was carried out to determine combining ability and association of yield and yield components among crosses derived from seven selected cowpea (Vigna unguiculata (L.) Walp) parents. Twenty-one hybrids were generated from diallel crosses excluding reciprocals. Hybrids along with seven parents were studied for combining ability and phenotypic correlations for seed yield and eight yield components. The result indicated that the general combining ability (gca) and specific combining ability (sca) were significant for most characters indicating the importance of both additive and non-additive genetic components. Additive gene action was important for eight characters except pod number, whereas non-additive gene action was not important for nodule number and grain yield. Parental lines IT86D-716 and IT81D-985 were found to be good general combiners for grain yield and other traits. The most promising specific combiners for yield and yield components were from crosses including IT87D-697-2 × IT86D-716, IT88D-867-11 × IT86D-716, IT93K-624 × IT87D-697-2, and IT87D-697-2 × IT92KD-405-1. Significant positive phenotypic correlations were observed between seed yield with pod length (POL), number of pods per plant (PON), and number of seeds per pod (SPD). POL, pod number per plant, SPD, and grain yield were identified as the best selection criteria that could be used in cowpea breeding programs.     

QTL mapping of pod tenderness and total soluble solid in yardlong bean [Vigna unguiculata (L.) Walp. subsp. unguiculata cv.-gr. sesquipedalis]

Yardlong bean [Vigna unguiculata ssp. unguiculata cv.-gr. sesquipedalis] is an important vegetable legume, particularly in Asia. Tenderness and sweetness of fresh pods are the key factors in deciding the commercial acceptance of yardlong bean. We report here for the first time quantitative trait loci (QTL) mapping of these traits from crosses between the yardlong bean accession JP81610 and wild cowpea (V. unguiculata ssp. unguiculata var. spontanea) accession JP89083. Two SSR-based linkage maps developed from BC₁F₁ [(JP81610?×?JP89083)?×?JP81610] and F₂ (JP81610?×?JP89083) populations were used for QTL analysis of pod tenderness and total soluble solid (TSS) content. Composite interval mapping (CIM) identified three QTLs for pod tenderness with phenotypic variance explained (PVE) of 5.6?C50?% and alleles from JP81610 increased the tenderness. CIM detected two QTLs for pod TSS with PVE of 7 and 9?%, and alleles from JP89083 increased TSS. Locations of these QTLs were compared with those of QTLs controlling domestication-related traits identified in the same populations. All QTLs for pod tenderness co-localized with QTLs for pod length. QTLs for pod TSS co-located with QTLs for pod dehiscence and/or pod length. The implications of these QTLs in breeding new yardlong bean and cowpea cultivars are discussed.     

Gene action and heritability for photosynthetic activity in two wheat crosses

Summary Gene action and heritability for photosynthetic activity were estimated from generation means in two wheat crosses during two stages (5 ^th leaf and flag leaf between 2 and 5 days after anthesis). Six generations were available for each cross: parents (P₁ and P₂), F₁, F₂ and backcrosses (BC₁ and BC₂).Correlations between some morphophysiological characters and photosynthetic activity of the flag leaf was also determined. The joint scaling test described by Mather & Jinks was used to determine the gene action. It showed that them; [d]; [h]; [i], [l] (mean, additivity, dominance, additive x additive interallelic interaction effects, dominance x dominance interallelic interaction effects) model fits the two crosses at both measurement times. All the model genetic components were significant for the flag leaf, however for the 5 ^th leaf only [h]; [i] and [l] were significant. The presence of additive and additive x additive effects suggested the possibility of selecting for this character using the flag leaf so as to obtain pure inbred lines. Dominance effects [h] were negative and dominance x dominance effects [l] were positive. Broad sense heritability values were medium to low. There were no correlations between the studied morphophysiological characters and the photosynthetic activity.     

Genetic analysis of yield and its components in vegetable cowpea (Vigna unguiculata L. Walp)

The F2 and backcrosses of a cross between two vegetable cowpea (Vigna unguiculata L. Walp) varieties with contrasting characteristics were evaluated for pod yield and its components, with the aim of understanding the genetic basis of these characteristics. A four-parameter model incorporating the additive, dominance and additive × additive genetic components fitted the data for pod yield and clusters per plant. The additive and additive × additive effects were positive and were larger than the dominance component. The relatively large additive and the predominantly positive dominant effects suggest that selection would be effective. Pod weight had high broad (84%) and narrow sense heritability (75%) and can be effectively selected for in the early generations. The study suggested that vegetable cowpea improvement programs should focus on selecting for clusters per plant and average pod weight in the early generations, while selection for dry pod yield could be delayed to later generations. It was concluded that pods per plant may be a useful selection criterion in multi-location trials aimed at selecting for stability of yield. This revised version was published online in July 2006 with corrections to the Cover Date.     

Inheritance pattern of mungbean yellow mosaic disease resistance and gene action for different traits in mungbean (Vigna radiata (L.) Wilczek) under protected and unprotected field conditions

Understanding of mungbean yellow mosaic disease resistance is crucial to develop resistant varieties to combat worldwide threat of the disease epidemics. This study was aimed to determine nature of disease resistance in terms of number of genes governing it and genetics of related traits. Experimental site was located on 31.43°N and 73.06°E with an elevation of 186 m, and evaluation trials were conducted during spring season due to high disease epidemics in this season. Two contrasting genotypes, that is, NM 6‐68‐2 (resistant) and NM 1‐32‐1 (highly susceptible), were crossed to raise six populations, that is, P₁, P₂, F₁, F₂, BC₁ and BC₂ for evaluation under protected and unprotected field conditions using chi‐square test and generation mean and variance analysis. It was discovered that disease resistance was governed by two major genes with additive effects. Disease resistance can easily be incorporated through backcrossing and direct selection following hybridization. Direct selection should be practised at earlier generation for plant height, chlorophyll contents and number of seeds per pod due to preponderance of additive effects whereas at later generations for seed yield per plant, 100 seed weight, harvest index, number of pods per plant and pod length due to involvement of duplicate epistasis.     

Genetics of grains per spike in durum wheat under normal and late planting conditions

Parental, F₁, F₂, BC₁, BC₂, BC₁₁, BC₁₂, BC₂₁, BC₂₂, BC₁ self and BC₂ selfed generations of three crosses involving six cultivars of durum wheat (Triticum durum Desf.) were studied for grains per spike under normal and late sown environments to analyze the nature of gene effects. A 10-parameter model did not fully account for the differences among the generation means. In two cases more complex interactions or linkage were involved in the inheritance of grains per spike in durum. Both digenic and trigenic epistatic interactions had a role in controlling the inheritance of grains per spike, however, trigenic interactions contributed more than digenic interactions. Non-fixable gene effects were many times higher than fixable ones in all three crosses and in both sowing environments indicating a major role of non-additive gene effects in the inheritance of this trait. Duplicate epistasis between sets of three genes under both environments was recorded for the cross Raj 911 × DWL 5002. Epistatic interactions, particularly the trigenic ones, contributed the maximum significant heterosis. Epistatic interactions involving dominance in the F₂ generations caused significant inbreeding depression. Selective diallel mating and/or biparental mating could be used for amelioration of grains per spike in durum wheat.     

Genetics of grain yield and other agronomic characters in t'ef (Eragrostis tef Zucc. Trotter). I. Generation means and variances analysis

Quantitative genetics of grain yield and other agronomic characters of t'ef (Eragrostis tef) were studied using the F₁, F₂, BC₁, and BC₂ of the cross Fesho × Kay Murri. The study was carried out to estimate gene effects controlling the inheritance of grain yield and related agronomic characters. Significant additive [d] and dominance × dominance [l] interaction effects were detected for grain yield. The variations of yield per panicle and panicle weight were explained in terms of [d], dominance [h], and additive × additive [i] interactions. Non-allelic gene interactions were also detected for kernel weight, harvest index, tiller number, plant height, days to heading and days to maturity. The simple additive-dominance model explained the variation for panicle length, culm diameter and plant weight, allowing unbiased estimates of additive (D) and dominance (H) variance components. Large dominance variances (H) were estimated for grain yield, yield per panicle, and panicle weight. The additive variances for plant height, panicle length, days to heading and days to maturity were higher than the respective dominance variances. High narrow-sense heritability (h²) values (> 0.50) were estimated for plant height, panicle length, days to heading and days to maturity. The lowest h² (0.09) was obtained for kernel weight for which there was little variability. Since grain yield and several important agronomic characters of t'ef are influenced by non-allelic gene interaction, it is advisable to delay selection for yield to later generations with increased homozygosity. This revised version was published online in July 2006 with corrections to the Cover Date.     

Genetics of resistance to early blight (Alternaria solani Sorauer) in tomato (Lycopersicon esculentum L.)

The genetic nature of early blight resistance in tomato was studied in three crosses at seedling and adult plant stages. A six generation mean analysis of the cross Arka Saurabh (susceptible) × IHR1939 (resistance) and its reciprocal cross revealed that the resistance to early blight was conferred by recessive polygenes at both seedling and adult plant stages. This polygenic early blight resistance revealed the importance of additive and additive × additive gene effects at seedling stage and higher magnitude of dominance and dominance× dominance gene effects at adult plant stage. Evaluation of parents, F₁, F₂ and backcross generations of IHR1816 (resistance) × IHR1939 (resistance) revealed that the early blight resistance genes in IHR1816 (Lycopersicon esculentum NCEBR-1) and IHR1939 (Lycopersicon pimpinellifolium L4394) are independent. This revised version was published online in July 2006 with corrections to the Cover Date.     

Genetic analysis of grain mould resistance in coloured sorghum genotypes

Grain moulds are a major constraint to sorghum production and to adoption of improved cultivars in many tropical areas. Information on the inheritance of grain mould reaction is required to facilitate breeding of resistant cultivars. The genetic control of grain mould reaction was studied in 7 crosses of 2 resistant sorghum genotypes. P₁, P₂, F₁, F₂, BC₁ and BC₂ families of each cross were evaluated under sprinkler irrigation for field grade and threshed grade scores and subjected to generation mean analysis. Frequency distributions for grain mould reaction were derived and F₂ and BC₁ segregation ratios were calculated. Grain mould reaction in crosses of coloured grain sorghum was generally controlled by two or three major genes. Resistance to grain moulds was dominant. Significant additive gene effects were also found in all cross/season combinations. Significant dominance effects of similar magnitude to additive effects were also observed in five out of ten cross/season combinations. Gene interactions varied according to the parents with both resistant and susceptible parents contributing major genes. Choice of parents with complementary resistance genes and mechanisms of resistance will be critical to the success of resistance breeding. This revised version was published online in July 2006 with corrections to the Cover Date.     

Genetic analysis of prolificacy in “Sikkim Primitive”—A prolific maize (Zea mays) landrace of North‐Eastern Himalaya

Prolificacy assumes significance for development of high‐yielding baby corn hybrids. “Sikkim Primitive” is a native landrace of North‐Eastern Himalaya, and is the highest prolific maize germplasm. So far, the genetics of prolificacy in “Sikkim Primitive” has not been deciphered. Here, a prolific inbred (MGU‐SP‐101) developed from “Sikkim Primitive” was crossed with four non‐prolific inbreds viz., LM13, BML7, HKI161 and HKI1128. Six generations (P₁, P₂, F₁, F₂, BC₁P₁ and BC₁P₂) of the crosses were evaluated at two locations during rainy season 2018. MGU‐SP‐101 possessed 2.50–3.78 ears per plant compared to 1.06–1.86 among non‐prolific inbreds. The variation for ears was the highest in F₂s (1–8), followed by BC₁P₁ (1–7) and BC₁P₂ (1–5). The quantitative inheritance pattern of prolificacy with prevalence of non‐allelic interactions of duplicate epistasis type has been observed. Dominance × dominance effect was predominant over additive × additive and additive × dominance effects. Total number of major gene blocks ranged from 0.41 to 2.86, thereby suggesting the involvement of at least one major gene/QTL governing the prolificacy. This is the first report of genetic dissection of prolificacy in “Sikkim Primitive”.     

Inheritance of drought resistance related traits in two crosses of groundnut (<Emphasis Type="Italic">Arachis hypogaea</Emphasis> L.)

Groundnut (Arachis hypogaea L.) is an important oilseed crop grown in more than 100 countries across wide range of environments. Frequent occurrence of drought is one of the limiting factors adversely affecting groundnut productivity, especially in rainfed areas, and hence genotypes having high water use efficiency (WUE) under limited available water need to be developed. In groundnut, WUE is correlated with SPAD chlorophyll meter reading (SCMR) and specific leaf area (SLA). These two traits, SCMR and SLA, can be used as surrogate traits for selecting for WUE. In order to improve SCMR and SLA, and in turn WUE in groundnut, a good knowledge of the genetic system controlling the expressions of these traits is essential for the selection of the most appropriate and efficient breeding procedure. The present investigation was conducted to determine the gene action controlling the inheritance of SCMR and SLA in two crosses, ICG 7243 × ICG 9418 and ICG 6766 × Chico, and their reciprocals. Six generations of each cross (P₁, P₂, F₁, F₂, BC₁P₁, and BC₁P₂) were evaluated for SCMR and SLA at two stages of the crop growth viz., 60 and 80 days after sowing (DAS). For SCMR at 80 DAS, additive effects were important in both the crosses whereas predominance of dominance effects with duplicate epistasis was observed for SCMR at 60 DAS and SLA at both stages in both the crosses. Predominance of additive effect for SCMR at 80 DAS suggested effective selection could be practiced even in early generations whereas for SCMR at 60 DAS and SLA at both stages in both crosses, it would be better to defer selection to later generations. Further, recording of SCMR and SLA should be done between 60 and 80 DAS for screening the germplasm lines for drought tolerance.     

Pattern of genetic inheritance of morphological and agronomic traits of sorghum associated with resistance to sorghum shoot fly, <Emphasis Type="Italic">Atherigona soccata</Emphasis>

Sorghum shoot fly, Atherigona soccata is an important pest of sorghum during the seedling stage, which influences both fodder and grain yield. To understand the nature of inheritance of shoot fly resistance in sorghum, we performed generation mean analysis using two crosses IS 18551 × Swarna and M 35-1 × ICSV 700 during the 2013–2014 cropping seasons. The F₁, F₂, BC₁ and BC₂ progenies, along with the parental lines were evaluated for agronomic and morphological traits associated with resistance/susceptibility to sorghum shoot fly, A. soccata. The cross IS 18551 × Swarna exhibited significant differences between the parents for shoot fly deadhearts (%) in the postrainy season. The progenies of this cross exhibited lower shoot fly damage, suggesting that at least one of the parents should have genes for resistance to develop shoot fly-resistant hybrids. Leaf glossiness, leafsheath pigmentation and plant vigor score during the seedling stage exhibited non-allelic gene interactions with dominant gene action, whereas 100 seed weight showed both additive and dominant gene interactions. Presence of awns showed recessive nature of the awned gene. Generation mean analysis suggested that both additive and dominance gene effects were important for most of the traits evaluated in this study, but dominance had a more pronounced effect.     

Genetics of Resistance in Vicia sativa L. to Orobanche crenata Forsk.

The genetics of resistance of common vetch (Vicia sativa L.) to broomrape (Orobanche crenata Forsk.) was studied for two years by using the P₁, P₂, F₁, BC¹, BC₂, F₂ F₃, and F₄ generations obtained from crosses between resistant and susceptible lines. Resistant lines were selected by screening a world collection m a naturally infested plot. Resistance was tested both under field and greenhouse conditions. The best index to measure resistance was the number of emerged broomrapes per host plant. The results fit the additive-dominance model. The main component of the variation was additivity; dominance and interaction effects seemed to depend on the environment. When dominance is expressed, a low number is dominant over a high number of broomrapes per host plant.     

Genetic analysis of yield and quantitative traits in pigeonpea (<Emphasis Type="Italic">Cajanus cajan</Emphasis> L. Millsp.)

Basic information on genetics and inheritance of quantitative characters, which is necessary to develop future breeding programme, is not widely studied in pigeonpea. Hence, present study was conducted among 5 generations in four pigeonpea crosses to know significance of additive-dominance model, gene action involved in inheritance of quantitative characters, heritability and genetic advance. “Scaling” and “joint scaling test” was significant for most characters indicating that additive-dominance model alone is not enough to explain the inheritance of a character. Though additive variance was more, dominance variance also played important role for most of the traits. Positive and negative alleles were found to be distributed between parents. Additive gene effect (d) was significant for pods per plant and seeds per pod whereas dominance gene effect (h) was more predominant among pod yield and seed yield. Dominance × Dominance inter-allelic interactions (l) was more important than Additive × Additive type (i) for most of the traits studied which could be exploited by selecting individuals based on their performance in recurrent selection. Complementary gene action was observed among many traits with few exhibiting duplicate gene action. Heritability and genetic advance was high indicating the effectiveness of selection. Since dominance effects is also present along with additive effects selection could be practised in later generations to identify high yielding genotypes.     

Involvement of higher order interactions addressing complex polygenetically controlled inheritance of downy mildew [Sclerospora graminicola (Sacc.) Schrot] resistance in pearl millet [Pennisetum glaucum (L.) R.Br.]

Inheritance of downy mildew [Sclerospora graminicola (Sacc.) Schrot]resistance was studied using generation mean analysis in pearl millet [Pennisetum glaucum (L.) R.Br.]. Eleven basic generations, namely, P₁, P₂, F₁, F₂, B₁, B₂, B₁F₂, B₂F₂, L₁, L₂ and L₃ of three crosses involving six diverse lines for downy mildew incidence were evaluated under artificial epiphytotic conditions over two environments. The downy mildew incidence was best fitting for digenic, trigenic and tetragenic ratios when fitted into classical Mendelian ratios demonstrating involvement of two or more genes. Digenic and trigenic interaction models were adequate in the case of crosses I and III respectively, to account for the total variability in generation means. Unlike severity, comparative estimates of gene effects over two environments were mostly consistent in all crosses for prevalence. Most of the epistatic and major gene effects were found significant in all crosses for both the disease traits. Non-allelic interactions particularly at three-gene loci viz., w (additive × additive × additive) and y (additive × dominance × dominance) in cross II and all trigenic interactions in cross III were predominant. Duplicate dominance (cross I) and complementary epistasis (crosses II and III) were observed for both the traits revealing inconsistency of gene effects over crosses. The gd₁ (interaction of additive gene effect with e₁) and gh₁(interaction of dominant gene effect with e₁) were significant in crosses I and II, indicating interaction of additive and dominance gene effects with environments. Thus a breeding method that can mop up the resistant genes to form superior gene constellations interacting in a favorable manner against pathotype I would be more suitable to accelerate the pace of resistance improvement. This revised version was published online in August 2006 with corrections to the Cover Date.     

Estimation of genetic components of variation for salt tolerance in chickpea using the generation mean analysis

Chickpea (Cicer arietinum L.) is known to be salt-sensitive and in many regions of the world its yields are restricted by salinity. Recent identification of large variation in chickpea yield under salinity, if genetically controlled, offers an opportunity to develop cultivars with improved salt tolerance. Two chickpea land races, ICC 6263 (salt sensitive) and ICC 1431 (salt tolerant), were inter-crossed to study gene action involved in different agronomic traits under saline and control conditions. The generation mean analysis in six populations, viz. P₁, P₂, F₁, F₂, BC₁P₁ and BC₁P₂, revealed significant gene interactions for days to flowering, days to maturity, and stem Na and K concentrations in control and saline treatments, as well as for 100-seed weight under salinity. Seed yield, pods per plant, seeds per plant, and stem Cl concentration were controlled by additive effects under saline conditions. Broad-sense heritability values (>0.5) for most traits were generally higher in saline than in control conditions, whereas the narrow-sense heritability values for yield traits, and stem Na and K concentrations, were lower in saline than control conditions. The influence of the sensitive parent was higher on the expression of different traits; the additive and dominant genes acted in opposite directions which led to lower heritability estimates in early generations. These results indicate that selection for yield under salinity would be more effective in later filial generations after gene fixation.     

Yield, yield components and plant architecture in the F3 generation of common bean (Phaseolus vulgaris L.) derived from a cross between the determinate cultivar ‘Prelude’ and an indeterminate landrace

Growth trials were conducted outdoors in the UK to determine the yield, yield components and plant architectural differences between determinate and indeterminate Phaseolus vulgaris bean plants. F3 lines derived from crosses between ‘Prelude’, a determinate cultivar and ‘V8’, an indeterminate landrace, were grown together with the parents and ‘Carioca’, an indeterminate landrace from Brazil. Data were recorded on flowering date, number of nodes on main stem at flowering, plant height at maturity, number of pods/plant, number of seeds/pod, number of seeds/plant, 100-seed weight, seed mass/plant, percentages of diseased and healthy seeds/plant. Determinate F3 lines had significantly lower (P < 0.05) seed mass/plant, fewer pods/plant, fewer seeds/pod, fewer seeds/plant, lower harvest index, shorter stems, earlier date of flowering, fewer nodes at flowering and fewer healthy seeds/plant than indeterminate F3 lines. However, determinate genotypes had significantly larger (P < 0.05) pods to accommodate their larger seeds compared with indeterminate lines. A similar situation was found when the yield and yield components of ‘V8’, ‘Prelude’ and ‘Carioca’ were evaluated; the highest seed mass/plant was given by ‘V8’ and the lowest by ‘Prelude’. Furthermore, some indeterminate genotypes with Type IV growth habit yielded significantly higher (P < 0.05) than the high-yielding parent, ‘V8’, indicating a positive influence on seed yield by crossing different genotypes.     

Genetic analysis of grain mold resistance in white seed sorghum genotypes

Grain molds in rainy season sorghums can cause poor grain quality resulting in economic losses. Grain molds are a major constraint to the sorghum production and for adoption of the improved cultivars. A complex of fungi causes grain mold. Information on genetics of grain mold resistance and mechanisms is required to facilitate the breeding of durable resistant cultivars. A genetic study was conducted using one white susceptible, three white resistant/tolerant sources, and one colored resistant source in the crossing programme to obtain four crosses. P₁, P₂, F₁, BC₁, and BC₂, and F₂ families of each cross were evaluated for the field grade and threshed grade scores, under sprinkler irrigation. Generation mean analyses and frequency distribution studies were carried out. The frequency distribution studies showed that grain mold resistance in the white-grained resistance sources was polygenic. The additive gene action and additive × additive gene interaction were significant in all the crosses. Simple recurrent selection or backcrossing should accumulate the genes for resistance. Epistasis gene interactions were observed in colored resistance × white resistance cross. Gene interaction was influenced by pronounced G × E. Pooled analysis showed that environment × additive gene interaction and environment × dominant gene interaction were significant. The complex genetics of mold resistance is due to the presence of different mechanisms of inheritance from various sources. Evaluation of segregating population for resistance and selection for stable derivatives in advanced generations in different environments will be effective.