Inheritance of black testa colour in lentil (Lens culinaris Medik.)

The inheritance of testa (seed coat) colour and interaction of cotyledon and testa colours were studied in seven crosses of lentil (Lens culinaris Medik.) involving parents with black, brown, tan or green testa and with orange, yellow or dark green cotyledons. Analysis of F₂ and F₃ seed harvested from F₁ and F₂ plants, respectively, revealed that although black testa is dominant over nonblack testa, its penetrance is not complete since both F₁ plants and heterozygous F₂ plants produced varying proportions of seeds with either black or nonblack testa. The F₂ populations of the crosses between parents with brown and tan, as well as brown and green, testa segregated in the ratio of 3 brown : 1 tan and 3 brown : 1 green, respectively, indicating monogenic dominance of brown testa colour over tan or green. The expression of testa colour was influenced by cotyledon colour when parents with brown or green testa are crossed with those having orange or green cotyledons. Thus F₂ seeds from these crosses with a green testa always had green cotyledons and never orange cotyledons. F₂ seeds from these crosses with a brown testa always had orange cotyledons and never green cotyledons. These results suggest diffusion of a soluble pigment from the cotyledons to the testa. This revised version was published online in July 2006 with corrections to the Cover Date.     

Inheritance of flower and pod colour in cowpea (Vigna unguiculata L. Walp.)

Inheritance of flower colour and pod colour in cowpea (Vigna unguiculata L. Walp.) has followed a qualitative pattern. Purple flower colour is dominant over white flower colour, whereas black pod colour is partially dominant over white pod colour. A segregation ratio of 3 purple:1 white flowers in F₂ generations of two crosses indicated that white flower colour is controlled by a single recessive. Segregation ratio of F₂ 1 white:2 light black:1 black indicated that black pod colour is partially dominant over white pod colour and is governed by one gene. These results were further confirmed by backcross generations. White flower and pod colour are controlled by single recessive genes on separate chromosome. Gene symbols were assigned. This revised version was published online in July 2006 with corrections to the Cover Date.     

Inheritance of petal colour and its independent segregation from seed colour in Brassica rapa

The inheritance of petal (flower) colour and seed colour in Brassica rapa was investigated using two creamy‐white flowered, yellow‐seeded yellow sarson (an ecotype from Indian subcontinent) lines, two yellow‐flowered, partially yellow‐seeded Canadian cultivars and one yellow‐flowered, brown‐seeded rapid cycling accession, and their F₁, F₂, F₃ and backcross populations. A joint segregation of these two characters was examined in the F₂ population. Petal colour was found to be under monogenic control, where the yellow petal colour gene is dominant over the creamy‐white petal colour gene. The seed colour was found to be under digenic control and the yellow seed colour (due to a transparent coat) genes of yellow sarson are recessive to the brown/partially yellow seed colour genes of the Canadian B. rapa cvs.‘Candle’ and ‘Tobin’. The genes governing the petal colour and seed colour are inherited independently. A distorted segregation for petal colour was found in the backcross populations of yellow sarson × F₁ crosses, but not in the reciprocal backcrosses, i.e. F₁× yellow sarson. The possible reason is discussed in the light of genetic diversity of the parental genotypes.     

Reciprocal cross differences in a 6×6 diallel set of groundnut (Arachis hypogaea L.) in the F1 generation

Summary Reciprocal cross differences were studied in a 6×6 diallel full set comprising of thirty hybrid combinations of groundnut in the F₁ generation.Reciprocal cross differences were observed for growth habit in four pairs of crosses, for leaf colour, flower colour and stem pigmentation in two pairs of crosses each. It was observed that the inheritance of flower colour, stem pigmentation and testa colour which exhibited different shades of purple colour was likely to be governed by pleiotropic gene(s). Among the quantitative characters significantly positive reciprocal effects were observed in different crosses for number of mature pods per plant, weight of pods per plant and shelling percent. Marked reciprocal cross differences were observed for pod and kernel characters like pod filling, pod beak, pod constriction and testa colour.     

Inheritance of neurotoxin (ODAP) content, flower and seed coat colour in grass pea (Lathyrus sativus L.)

Summary A strong epidemiological association is known to exist between the consumption of grass pea and lathyrism. A neurotoxin, -N-Oxalyl-L-, -diaminopropanoic acid (ODAP) has been identified as the causative principle. This study was undertaken to investigate the mode of inheritance of the neurotoxin ODAP, flower and seed coat colour in grass pea. Five grass pea lines with low to high ODAP concentration were inter-crossed in all possible combinations to study the inheritance of the neurotoxin. Parents, F₁ and F₂ progenies were evaluated under field condition and ODAP analyzed by an ortho-phthalaldehyde spectrophotometric method. Many of the progenies of low x low ODAP crosses were found to be low in ODAP concentration indicating the low ODAP lines shared some genes in common for seed ODAP content. The F₁ progenies of the low ODAP x high ODAP crosses were intermediate in ODAP concentration and the F₂ progenies segregated covering the entire parental range. This continuous variation, together with very close to normal distribution of the F₂ population both of low x low and low x high ODAP crosses indicated that ODAP content was quantitatively inherited. Reciprocal crosses, in some cases, produced different results indicating a maternal effect on ODAP concentration. Blue and white flower coloured lines of grass pea were inter-crossed to study the inheritance of flower colour. Blue flower colour was dominant over the white. The F₂ progenies segregated in a 13:3 ratio indicating involvement of two genes with inhibiting gene interactions. The gene symbol LB for blue flower colour and LW for white flower colour is proposed.     

Inheritance of seed colour in Brassica campestris L. and breeding for yellow-seeded B. napus L.

Summary Seed colour inheritance was studied in five yellow-seeded and one black-seeded B. campestris accessions. Diallel crosses between the yellow-seeded types indicated that the four var. yellow sarson accessions of Indian origin had the same genotype for seed colour but were different from the Swedish yellow-seeded breeding line. Black seed colour was dominant over yellow. The segregation patterns for seed colour in F₂ (Including reciprocals) and BC₁ (backcross of F₁ to the yellow-seeded parent) indicated that the black seed colour was conditioned by a single dominant gene. Seed colour was mainly controlled by the maternal genotype but influenced by the interplay between the maternal and endosperm and/or embryonic genotypes. For developing yellow-seeded B. napus genotypes, resynthesized B. napus lines containing genes for yellow seed (Chen et al., 1988) were crossed with B. napus of yellow/brown seeds, or with yellow-seeded B. carinata. Yellow-seeded F₂ plants were found in the crosses that involved the B. napus breeding line. However, this yellow-seeded character did not breed true up to F₄. Crosses between a yellow-seeded F₃ plant and a monogenomically controlled black-seeded B. napus line of resynthesized origin revealed that the black-seeded trait in the B. alboglabra genome was possibly governed by two independently dominant genes with duplicated effect. Crossability between the resynthesized B. napus lines as female and B. carinata as male was fairly high. The sterility of the F₁ plants prevented further breeding progress for developing yellow-seeded B. napus by this strategy.     

Inheritance of siliqua characters in Indian colza I. Locule number and siliqua position

Summary F₁, F₂, BC₁ and BC₂ generations, involving bilocular and tetralocular siliquae and with upright and pendent siliqua position, were studied with their parents. The segregation pattern in these generations indicated that number of locules is monogenically governed with the allel for bilocular type (VV-two valved pods) showing complete dominance over tetralocular (vv). Upright siliqua position is governed by two dominant genes (Up₁ Up₁ Up₂ Up₂) and pendent by two recessive genes (up₁ up₁ up₂ up₂). However, in absence of even a single dominant gene it give rise to a third type of siliqua position i.e. parallel.     

The increase of seed fertility of Brassicoraphanus through cytological irregularity

Summary Amphidiploids (Brassicoraphanus) were produced by means of colchicine treatment of F₁ hybrids between Brassica japonica Sieb. and Raphanus sativus L. The cytology of the amphidiploids was studied from F₁ to F₃ generations. Some plants had the euploid chromosome number 2n=38, whereas others had the aneuploid number 2n=37. One or two of either quadrivalents or trivalents, as well as some univalents, were seen in most of the plants examined. All the plants showed a low seed fertility. In F₃ generation there arose some yellow-flowered plants, all of which showed a higher seed fertility than normal white-flowered plants. It is postulated that the change of flower colour might originate in the segmental exchange of only partially homologous chromosomes following multivalent formation. A gene causing white flower colour was perhaps closely linked to a gene causing sterility, and both genes were probably excluded together through the segmental exchange of the chromosomes. Therefore, it can be said that the increase of fertility was induced by cytological irregularity.     

Genetic variation in tannin-related characters of faba-bean seeds (Vicia faba L.) and their relationship to seed-coat colour

Tannin content and tanning power on haemoglobin were evaluated in a collection of faba-bean genotypes differing in seed and flower colour. All tannin-related measurements gave near-zero values for white-flowered genotypes; they showed intermediate values in brown and green-seeded genotypes, brown being lower in tannin values than green. Genetic analysis in the F₃ of a half-diallel design confirmed the strong link between brown and green testa colour and intermediate tanning activities.     

Genetics of seed coat colour in lentil

Summary Four grey mottled seed coat colour lentil lines/cultivars were crossed to one brown seed coat colour cultivar. The F₁ hybrids were brown seeded in all the crosses. Segregation pattern for seed coat colour in F₂ and F₃ generations revealed that it is under control of a single dominant gene, which is present in the parent UPL 175 while a recessive gene is responsible for grey mottled seed coat colour in Pant L 406, Pant L 639, LG 120 and Rau 101.     

Inheritance of siliqua orientation and seed coat colour in Brassica tournefortii

The inheritance of siliqua orientation and seed coat colour in Brassica tournefortii was investigated using four genotypes varying in these two characters. The F₁, F₂ and backcross generations of two crosses were used for studying the segregation pattern of the traits. The plants were classified for seed colour as having brown or yellow seeds and for siliqua orientation as having upright, semi‐spread or spread siliqua. Seed colour was found to be under monogenic control with brown being dominant over yellow. Siliqua orientation was under digenic polymeric gene action: upright siliqua was produced by the presence of two dominant genes and spread siliqua by two recessive genes. The absence of even a single dominant gene resulted in a third type of siliqua orientation, semi‐spread siliqua.     

Single gene mutation for green cotyledons as a marker for the embryonic genotype in faba bean, Vicia faba

A new spontaneous mutation is described in faba bean, Vicia faba L., characterized by a marked green colour in the entire cotyledon tissues of the mature seeds, while the wild phenotype is yellow. This seed character reflects the embryonic genotype and is determined by a single recessive allele named i1-1. It is distinct from the y gene, which codes for green testa. As is the case for gene y, the gene i1-1 displays no epistatic effects with the zero-tannin genes zt1 and zt2 which influence seed and flower colour in faba bean. In this allogamous species, such a mutation is a useful tool in cross-fertilization studies.     

Inheritance of two components of early maturity in groundnut (Arachis hypogaea L.)

Summary Knowledge of inheritance of early maturity or its components is important to groundnut breeders in developing short-duration cultivars. This study was conducted to determine the inheritance of two components of early maturity: days to first flower from sowing, and days to accumulation of 25 flowers from the appearance of first flower, using three groundnut genotypes. Two early-maturing (Chico and Gangapuri) and one late-maturing (M 13) genotypes were crossed in all possible combinations, including reciprocals. The parents, F₁, F₂, F₃, and backcross populations were evaluated for days to first flower from sowing, and for days to accumulation of 25 flowers. The data suggest that days to first flower in the crosses studied is governed by a single gene with additive gene action. Chico and Gangapuri possess the same allele for this component of earliness. Three independent genes with complete dominance at each locus appear to control the days to accumulation of 25 flowers. In crosses between late (M 13) and early (Chico or Gangapuri) parents, a segregation pattern suggesting dominant-recessive epistasis (13 late:3 early) was observed for this component. Segregation in the F₂ generation (1 late:15 early) of both early parents (Chico x Gangapuri) indicated that the genes for early accumulation of flowers in these two parents are at different loci.Submitted as ICRISAT J.A. No. 1557.     

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.     

Models of inheritance of flower colour and extra petals in Potentilla fruticosa L.

Summary Inheritance models for flower colour and extra petals in Potentilla fruticosa L. were developed by conducting controlled crosses between different cultivars and advanced selections. Parents were crossed in all combinations and floral character segregation of progenies were recorded. Preliminary models for flower colour include two whitening genes (W₁ and W₂) and two yellowing genes (Y₁ and Y₂) with the action of a bleaching gene also implicated. The cyanic flower colour model developed involves background petal colour, cyanic pigments and distribution and temperature sensitivity genes. The extra petals model involves a two gene switch, D₁ and D₂ to turn on the production of up to five extra petals and a modifier gene, D_m that accounts for an additional one to five extra petals. Either D₁ or D₂ must be recessive to initiate extra petal production. D_m must also be recessive to enable production of an additional 1–5 petals.     

玉米茎秆糖含量的遗传模式分析

较高的茎秆糖含量有助于提高青贮玉米的饲料品质和适口性,本研究以YXD053和98A-04两个高茎秆糖含量玉米自交系为母本,Y6-1低茎秆糖含量玉米自交系为父本,通过自交、杂交及回交产生2个组合的6个世代(P₁、P₂、F₁、F₂、BC₁和BC₂);运用主基因+多基因混合遗传模型6个世代联合分析方法,探明控制玉米茎秆糖含量的遗传模型,并进行遗传参数估计。结果表明,玉米茎秆糖含量遗传受2对加性-显性-上位性主基因+加性-显性-上位性多基因共同控制。YXD053×Y6-1及98A-04×Y6-1两个组合的主基因遗传率分别为53.50%和52.63%,多基因遗传率分别为7.96%和17.31%,总遗传率分别为61.46%和69.94%,显性度(h/d)均小于1。茎秆糖含量以主基因遗传为主,且主基因又以加性效应为主,但环境因素对茎秆糖含量的遗传有一定的影响。这一研究结果为玉米茎秆糖含量性状的基因定位和育种选择提供了理论依据。     

The inheritance of apetalous flower type in Petunia hybrida Vilm. and linkage tests with the genes for flower doubleness and grandiflora characters and its use in hybrid seed production

Summary Genetic analysis of a mutant flower form in petunia in which the normal corolla tube was replaced by a second set of sepals (apetalous condition) was studied in F₁, F₂, F₃ and BC₁ generations after crossing with inbred normal flowered lines. Segregation patterns observed in these generations indicated that this mutant flower type was a monogenic recessive trait. The genes D for flower doubleness and G for grandiflora plant and flower character segregated independent of the apetalous character. The gene for apetalous flower character has been designated as apt.Michigan Agricultural Experiment Station Journal Article No 6272.     

Inheritance and mapping of male sterility restoration gene in upland japonica restorer lines

Several upland Japonica breeding lines, WAB450-11-1-3-P40-HB (Abbreviated as WAB450-11), WAB450-11-1-2-P61-HB (WAB450-13), WAB450-l-B-P-91-HB (WAB450-14), IRAT216, IRAT359, and IRAT104, possessing restoring ability for the Dian 1 type cms (cms-D) line Dianyu 1A were recently identified at Food Crops Research Institute, Yunnan Academy of Agricultural Sciences, P. R. China. In this study, the inheritance of restoring ability in these lines was characterized through the production of backcross populations to the male-sterile and maintainer Dianyu 1 lines. Each of the restorer lines was used to pollinate Dianyu 1A to form a F₁ hybrid which was then backcrossed (1) with Dianyu 1B producing a BC₁F₁ population and (2) to the female parent Dianyu 1A producing a BC₅F₂ population. The lines were also crossed with the japonica restorer line C57, carrying the restorer gene Rf1 that was introgressed from indica, to form F₁ hybrids, these hybrids were then testcrossed with Dianyu 1A to study the allelic relationship of their restorer genes to Rf1. The inheritance in these testcross populations indicated that the complete restoring ability of WAB450-11, WAB450-13, WAB450-14, IRAT216, IRAT359, and the partial restoring ability of IRAT104 were controlled by dominant genes, and the gene in WAB450-13, WAB450-14, and IRAT216 was allelic or identical to Rf1. When 136 SSR markers were used to score 143 BC₁F₁ individuals from Dianyu 1A/WAB450-13//Dianyu 1B, the japonica Rf1 allele was found to be located between RM171 and RM6100 on the long arm of chromosome 10, an interval corresponding to that known for the indica Rf1 allele. The distance between RM171 and Rf1 is 2.8 cM, and that between Rf1 and RM6100 is 4.9 cM. Similar linkage results were obtained from mapping 89 individuals of the corresponding BC₅F₂ population (Dianyu 1A/6/Dianyu 1A/WAB450-13).     

Inheritance of seedling colour in faba bean (Vicia faba L.)

Summary The inheritance of purple seedling colour was studied, in relation to the genetic control of flower colour. It was found that purple seedling colour is likely to be controlled by a single gene and that the trait is dominant over green seedling colour. White flowering prohibited the expression of the purple seedling colour, and is therefore thought to be epistatic.This character can be used to estimate rate of outcrossing in breeding programmes, as well as contribute to our knowledge of the biosynthesis of plant pigments and secondary metabolites such as tannins.     

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.