Identification and mapping of a quantitative trait locus controlling extreme late bolting in Chinese cabbage (Brassica rapa L. ssp. pekinensis syn. campestris L.) using bulked segregant analysis

DNA markers linked to a locus controlling an extreme late bolting trait, which was originally found in a local cultivar of a non-heading leafy vegetable,‘Osaka Shirona Bansei’ (Brassica rapa L. ssp. pekinensis syn. campestris L.) were identified using bulked segregant analysis. A doubled haploid (DH) line, DH27, which is a progeny of ‘Osaka Shirona Bansei’, shows extreme late bolting, and bolts without vernalization. DH27 was crossed with a normal bolting DH line, G309. The plantlets of the parents, F₁ and F₂, were vernalized and then grown in a greenhouse. The bolting time of F₂ plants showed a continuous distribution from 19 to 231 days after vernalization (DAV), suggesting the effects of a few major genes and polygenes. Possible linkage markers for this trait were screened by modified bulked segregant analysis (BSA). The BSA using four bulks suggested that a 530-bp RAPD band RA1255C was linked to a locus controlling the bolting trait. The RAPD band was cloned and used as a probe to detect RFLP. The fragment detected a single locus, BN007-1,the segregation of which in the F₂ population matched that of RA1255C. Three other RAPDs were found to be linked to BN007-1. A quantitative trait locus(QTL) affecting the bolting time was detected around BN007-1 using MAPMAKER/QTL. Since the difference between bolting times of both the parental genotypes in the F₂ was 138 days, these markers may be useful for a marker-assisted selection (MAS) in the breeding program for late bolting or bolting-resistant cultivars in B. rapa crops. This revised version was published online in July 2006 with corrections to the Cover Date.     

Inheritance of internal pigmentation in green cabbage (Brassica oleracea var. Capitata L.)

Summary Internal anthocyanin pigmentation (IP) in otherwise normally green cabbage occurs in a number of Oregon State University breeding lines. Extracted pigment, tested for spectral absorption and for color reactions with lead acetate and aluminium chloride, was similar but not necessarily identical to pigment extracted from red cabbage cultivar Redman. When IP line R52 was crossed with normal green line C70, the F₁, F₂ and backcross progenies indicated that IP at the intensity found in R52 was determined by a single factor in homozygous condition, with intermediate levels of IP expressed by the heterozygous genotypes. Modifying factors also appear to influence the level of IP. In the cross R52 (IP)×R51 (normal green), expression of IP in the F₁ was much reduced. The F₂ failed to fit the expected 3 IP: 1 green ratio due to an excess of green plants, but instead, closely fit a 9:7 ratio. This may have resulted from incomplete expression of IP because of modifiers, rather than from the effects of a second major gene. An allele at the A (anthocyanin) locus of B. oleracea is tentatively proposed and designated A ^IP or a ^IP pending further identification.Oregon Agricultural Experiment Station Technical Paper No. 4690.     

SSR marker tightly linked to the Ti locus in Soybean [Glycine max (L.) Merr.]

Soybean is a major source of protein meal in the world. Soybean kunitz trypsin inhibitor (SKTI) protein is a responsible for the inferior nutritional quality of unheated or incompletely heated soybean meal. The primary objective of this research was to identify DNA markers linked to the Ti locus controlling presence and absence of kunitz trypsin inhibitor protein. Two mapping populations were developed. Population 1 was derived from a cross between cultivar Jinpumkong2 (TiTi) and C242 (titi). Population 2 was made from a mating between cultivar Clark (TiTi) and C242. The F₁ plants were grown in the greenhouse to produce F₂ seeds. Each F₂ seed from F₁ plants was analyzed electrophoretically to determine the presence of the SKTI protein band. One-thousand RAPD primers, 342 AFLP primer sets, and 35 SSR primers were used to map Ti locus in population 1 and 2. The presence of SKTI protein was dominant to the lack of a SKTI protein and kunitz trypsin inhibit protein band was controlled by a single locus. Twelve DNA markers (4 RAPD, 4 AFLP, and 3 SSR) and Ti locus were found to be genetically linked in population 1 consisted with 94 F₂ individual plants. Three SSR markers (Satt409, Satt228, and Satt429) were linked with Ti locus within 10 cM. Satt228 marker was tightly linked with Ti locus. Satt228 marker was tightly linked within 0–3.7 cM of the Ti locus and may be useful in a marker assisted selection program.     

Hybridization of Sinapis alba L. and Brassica napus L. via Embryo Rescue

Embryo rescue techniques were used to obtain hybrids between Sinapis alba L. (white mustard) and Brassica napus L. (oilseed rape) with the goal of improving the disease tolerance of oilseed rape. Hybrid plants with 31 or 43 chromosomes were only recovered, when S. alba, was used as the female parent. One hybrid was obtained from the cross S. alba L. cv. ‘Kirby’×B. napus L. cv. ‘Topas’, while 26 hybrids were obtained, when various S. alba L. cultivars were pollinated with the rapid cycling B. napus line CrGC 5006. All F₁, hybrid plants were male sterile; however, the first generation backcross to B. napus L., also obtained by embryo rescue, produced plants with 50 chromosomes and 61–84 % pollen viability. Second backcross generation seed was produced by normal sexual crossing. Preliminary cytological analyses of pollen mother cells of hybrid plants suggests the possibility of genetic exchange between the two species.     

Molecular mapping of black rot resistance locus Xca1bo on chromosome 3 in Indian cauliflower (Brassica oleracea var. botrytis L.)

Black rot is the most devastating disease of cauliflower worldwide causing severe damage to crop. The identification of markers linked to loci that control resistance can facilitate selection of plants for breeding programmes. In the present investigation, F₂ population derived from a cross between ‘Pusa Himjyoti’, a susceptible genotype, and ‘BR‐161’, a resistant genotype, was phenotyped by artificial inoculation using Xcc race 1. Segregation analysis of F₂ progeny indicated that a single dominant locus governed resistance to Xcc race 1 in ‘BR‐161’. Bulk segregant analysis in resistant and susceptible bulks of F₂ progeny revealed seven differentiating polymorphic markers (three RAPD, two ISSR and two SSR) of 102 markers screened. Subsequently, these markers were used to genotype the entire F₂ population, and a genetic linkage map covering 74.7 cM distance was developed. The major locus Xca1bo was mapped in 1.6‐cM interval flanked by the markers RAPD 04₈₃₃ and ISSR 11₆₃₅. The Xca1bo locus was located on chromosome 3. The linked markers will be useful for marker‐assisted resistance breeding in cauliflower.     

A new resistance gene to PepYMV (Pepper yellow mosaic virus) in Capsicum annuum L.

Pvr4 locus, commonly associated with a co-dominant CAPS marker, confers monogenic dominant resistance to potyvirus complex in Capsicum spp. Aiming to investigate whether the resistance found in resistant genotypes not bearing Pvr4 marker is due to allelism in the Pvr4 locus, or due to a new locus of the pvr series, segregation analyses of an F₂ population obtained from a cross between two pepper lines “Myr-29-10” (P₁) (resistant to PepYMV, showing a single band of 444 bp, Pvr4/Pvr4) and “PIM-025” (P₂) (resistant to PepYMV, showing a single band of 458 bp, Pvr4⁺/Pvr4⁺) were performed. According to the results, there is strong evidence that the locus controlling PepYMV resistance in PIM-025 (P₂) is not Pvr4. These results provide evidence that those resistant genotypes, bearing a susceptible band pattern in the Pvr4 locus (458 bp, Pvr4⁺/Pvr4⁺), carry a different gene from those described in the literature up to the present time.     

38–48 kDa subunits of buckwheat 13S globulins are controlled by a single locus

The inheritance of buckwheat (Fagopyrum esculentum Moench) seed storage proteins was investigated by control crosses between accessions containing different SDS‐PAGE protein patterns in the range of 38–48 kDa. Analysis of segregation of individual F₁ and F₂ seeds obtained by 17 crosses showed segregation of eight electrophoretic bands, from which 12‐banding variants were inferred. Two variants contained one band, nine contained two bands and one variant contained three bands and behaved as a single co‐dominant unit. The segregation of banding variants fits the expected ratios and thus supports the hypothesis of single Mendelian gene inheritance and that alleles are co‐dominant. The results therefore suggest that the genes controlling globulin subunits are tightly linked and inherited as a single locus. The locus was designated Glob‐1 and the twelve segregated protein variants as alleles a‐l. This is the first buckwheat globulin locus identified with multiple alleles, phenotypically expressed as groups of protein bands and thus applicable as a functional marker in buckwheat genomic studies.     

The allelic relationship between A IP(internal pigmentation) and A RC (red cabbage) in Brassica oleracea var. capitata L.

Summary Internal anthocyanin pigmentation (IP), previously reported to be controlled by a single gene dominant to aa of normal green cabbage, was studied further to determine its relationship to A ^RC A ^RC of red cabbage. When IP line R52 was crossed with an early red cabbage line. F₁ heads were pigmented throughout, but pigment intensity was intermediate. Subjective classification of F₂ plants by pigmentation intensity and distribution scores gave a ratio of 1 intense red throughout (red cabbage):2 medium red throughout:1 medium to light red, restricted to the central portion of the head (IP). The genotypes A ^RC A ^RC: A ^RC A ^IP: A ^IP A ^IP. respectively, are proposed to explain these 3 phenotypic classes. F₂ progenies contained no normal green plants, supporting the conclusion that A ^IP and A ^RC are alleles.Technical Paper 7052, Oregon Agricultural Experiment Station.     

Evidence for the production of unreduced gametes by tetraploid Rosa hybrida L.

The objective of this study was to determine the mode of inheritance of field resistance to downy mildew (Peronospora parasitica (Pers. ex Fr.) Fr.) in broccoli (Brassica oleracea var.italica) at the adult plant stage. The F₁, F₂ and F₃ progeny of resistant and susceptible plants of broccoli were tested in the field under natural infection, in central Portugal, from August to December in two successive years. The plants were evaluated for resistance to downy mildew at maturity using a five-class scale of increasing susceptibility to the disease, which took into account the number of infected leaves and the size of the sporulating lesions. The F₁ was completely resistant, the F₂ segregated a clear 3 resistant: 1susceptible and the F₃ confirmed the F₂ segregation, which suggests a dominant character controlled by a single locus. This resistance has good potencial for direct use in commercial broccoli breeding or for transfer to other Brassica vegetables. This revised version was published online in August 2006 with corrections to the Cover Date.     

Relationship between tolerance and resistance to pepper mottle virus in a cross between Capsicum annuum L. × Capsicum chinense Jacq.

Summary Progenies of a cross between pepper cultivar Delray Bell (Capsicum annuum L.) tolerant to pepper mottle virus (PeMoV) and P.I. 159236 (Capsicum chinense Jacq.), resistant to PeMoV were evaluated in greenhouse experiments. The F₁ generation was susceptible to PeMoV, whereas the backeross generations to both parents and the F₂ segregated in a ratio of 1:1. This indicates that PeMoV resistance is controlled at the same locus in both parents or at two closely linked loci. Each parent is homozygous for one locus and the homozygous condition of either allele results in failure to support virus; in heterozygous condition as observed in the F₁ generation, the effect of a single allele is insufficient even when one allele of each type is present, resulting in systemic infection.The abstract of this paper was presented at the IVth Eucarpia Capsicum meetings held in October at Wageningen, Netherlands.Florida Agricultural Experiment Stations Journal Series Paper No. 3175.     

Inheritance studies with nine characters in Capsicum annuum L.

Summary Information obtained from breeding work with relatively small F₂ populations suggests independent segregation in 12 pairs of characters. Anthocyanin pigmentation in the cotyledon is either recessive or dominant, showing either single gene or polygenic inheritance, depending on parental genotypes. When single gene inheritance was observed, pigmentation was independent of resistance to potato virus-y, of the male sterile-1 (ms1) gene and of male sterile-2 (ms2) gene. However, additional observation suggests that one of the genes involved in pigmentation is linked with the male sterile-1 gene.     

Inheritance of resistance to angular leaf spot in Nicotiana tabacum L. cultivars burley 21 and kentucky 14

Summary The genetics of resistance to angular leaf spot caused by Pseudomonas syringae pv. tabaci in Nicotiana tabacum cultivars Burley 21 and Kentucky 14 was investigated by studying disease reactions to three isolates of parental, F₁, F₂ and backcross generations derived from crosses between the resistant cultivars and the susceptible cultivar Judy's Pride. Studies were conducted in the greenhouse and in field plant beds. Chi-square values were computed to determine whether the observed ratios for disease reactions deviated from expected Mendelian ratios for a single, dominant gene controlling resistance to angular leaf spot in tobacco. Based on the resistance of the F₁ and the backcross generation to the resistant parent (BC-R), a 3 resistant: 1 susceptible segregation ratio in the F₂, and a 1 resistant: 1 susceptible segregation ratio in the backcross generation to the susceptible parent (BC-S), it was concluded that resistance to three isolates of Pseudomonas syringae pv. tabaci is governed by a single, dominant gene.     

Major gene control of tolerance of bread wheat (Triticum aestivum L.) to high concentrations of soil boron

Summary The genetic control of tolerance of wheat to high concentrations of soil boron was studied for five genotypes. Each genotype represented one of five categories of response to high levels of boron, ranging from very sensitive to tolerant. Tolerance to boron was expressed as a partially dominant character, although the response of an F₁ hybrid, relative to the parents, varied with the level of boron applied. The F₁ hybrids responded similarly to the more tolerant parent at low B treatments and intermediate to the parents at higher treatments. Ratios consistent with monogenic segregation were observed for the F₂ and F₃ generations for the combinations (WI^*MMC) × Kenya Farmer, Warigal × (WI^*MMC) and Halberd × Warigal. The three genes, Bo1, Bo2 and Bo3, while transgressive segregation between two tolerant genotypes, G61450 and Halberd, suggested a fourth locus controlling tolerance to boron.     

Chromosome arm location of the gene controlling leaf pubescence of a Chinese local wheat cultivar ‘Hong-mang-mai’

The inheritance of the leaf pubescence character of a Chinese local wheat cultivar ‘Hon-mang-mai’ was investigated by monosomic and telosomic analyses. Leaf pubescence was evaluated by observation of the adaxial side of the penultimate leaf of adult plants. F₁ hybrids of ‘Hong-mang-mai’ with a non-pubescent cultivar ‘Chinese Spring’ had leaf pubescence, but its density was about a half of that of ‘Hong-mang-mai’. In the F₂ generation, the segregation ratio of pubescent to non-pubescent plants fitted a ratio of 3: 1, suggesting that leaf pubescence was controlled by one dominant gene. Monosomic analysis revealed that the gene for pubescence is located on chromosome 7B. Telosomic analysis showed that the gene is located on the short arm of chromosome 7B with a distance of 14.3%from the centromere. This gene is not allelic with the previously reported hairy leaf gene Hl on chromosome 4B, and therefore, is designated Hl2, hairy leaf 2. This revised version was published online in July 2006 with corrections to the Cover Date.     

A genetic analysis of self-incompatibility and double flowers in Potentilla fruticosa L.

Summary The self-incompatibility system in Potentilla fruticosa was investigated by examining pollen cytology, and by analysing intercrosses between two self-incompatible, cross-compatible cultivars of the species. The pollen was found to be binucleate, which is consistent with a single locus self-incompatibility system acting gametophytically in the pollen. This was confirmed by the results of the intercrosses. A proposed model for the inheritance of extra petals was tested by backcrossing selected F₁ hybrid plants to both of their parents. Non-random segregation of the double modifier (Dm) locus suggested linkage to the self-incompatibility locus (S). The model was accordingly modified to include this linkage.     

Inheritance of resistance to Puccinia coronata var. avenae in six selections of Avena sterilis

Summary Six selections of Avena sterilis, introduced from Israel as sources of resistance to oat crown rust, were crossed with susceptible A. byzantina Frazier. The number of genes conditioning resistance to culture H-14 of race 326 of Puccinia coronata var. avenae in each of the six selections was determined from studies of F₁, F₂ and F₃ populations from the crosses. P.I. 287211, P.I. 295919 and P.I. 296244 each appeared to have a single dominant gene for resistance, and P.I. 296265 and P.I. 296266 each two dominant ones. C.I. 8295 had a single partially dominant gene for resistance. Crosses among the A. sterilis parents indicated that at least four different genes conditioned resistance to culture H-14.Association between F₂ reaction to crown rust and morphological characters of the spikelet was determined with the % MathType!MTEF!2!1!+-% feaafiart1ev1aaatCvAUfeBSjuyZL2yd9gzLbvyNv2CaerbuLwBLn% hiov2DGi1BTfMBaeXatLxBI9gBaerbd9wDYLwzYbItLDharqqtubsr% 4rNCHbGeaGak0dh9WrFfpC0xh9vqqj-hEeeu0xXdbba9frFj0-OqFf% ea0dXdd9vqaq-JfrVkFHe9pgea0dXdar-Jb9hs0dXdbPYxe9vr0-vr% 0-vqpWqaaeaabaGaaiaacaqabeaadaqaaqaaaOqaaiabeE8aJnaaCa% aaleqabaGaaGOmaaaaaaa!39FC!\[\chi ^2 \] test for independence. In four crosses, all spikelet characters appeared to be independent of rust reaction. In Frazier x P.I. 296244, basal pubescence of the lemma on the secondary floret appeared to be associated with reaction to crown rust. Strong association between reaction to crown rust and lemma pubescence on the primary floret was evident in Frazier x P.I. 296265.     

Construction of a chromosome-assigned,sequence-tagged linkage map for the radish,Raphanus sativus L. and QTL analysis of morphological traits

The radish displays great morphological variation but the genetic factors underlying this variability are mostly unknown. To identify quantitative trait loci (QTLs) controlling radish morphological traits, we cultivated 94 F₄ and F₅ recombinant inbred lines derived from a cross between the rat-tail radish and the Japanese radish cultivar ‘Harufuku’ inbred lines. Eight morphological traits (ovule and seed numbers per silique, plant shape, pubescence and root formation) were measured for investigation. We constructed a map composed of 322 markers with a total length of 673.6 cM. The linkage groups were assigned to the radish chromosomes using disomic rape-radish chromosome-addition lines. On the map, eight and 10 QTLs were identified in 2008 and 2009, respectively. The chromosome-linkage group correspondence, the sequence-specific markers and the QTLs detected here will provide useful information for further genetic studies and for selection during radish breeding programs.     

Genetic characterization of the red coloured corolla phenotype for Gossypium arboreum accession PI 529731

Flower corolla colour is an important trait for the attraction of pollinators and for the horticultural industry. Gossypium arboreum (L.) accessions from the United States Department of Agriculture germplasm collection frequently show flowers with a yellow coloured corolla. Accession PI 529731 is unique in that the flowers have a red coloured corolla. Genetic characterization of corolla pigmentation was conducted by crossing PI 529731 with two white flower accessions. Flowers with a red corolla were observed in the F₁ generations suggesting a dominant trait. Variation in corolla colour was observed for plants in the F₂ populations including dark red, red, light red, white, yellow and white with petals having red coloured margins. These data support a single dominant gene conferring the four red corolla phenotypes. The yellow corolla phenotype also supported a single dominant gene model. Dominant alleles at both loci are required for expression of the PI 529731 phenotype and data support a two gene model with a 9:3:3:1 segregation ratio. These data are useful for the characterization of genetic mechanisms controlling tissue‐specific pigmentation.     

Cytogenetic studies on the interspecific hybrid Capsicum baccatum L.× C. frutescens L. and its progeny

Summary Morphological and cytogenetical studies were carried out on the F₁ and F₂ hybrids and backcross derivatives of the interspecific cross Capsicum baccatum L. x C. frutescens L. The F₁ and F₂ hybrids displayed irregular meiosis with a maximum association of eight chromosomes in the former and one quadrivalent in the latter with the appropriate number of bivalents and univalents. It is inferred that C. baccatum differs from C. frutescens (yellow) by at least tow or three interchanges and from the white cultivar by a single interchange. Structural repatterning of chromosomes, erratic meiotic behaviour, genes for pollen sterility, segregational imbalances following intergenomic recombination are believed to be major factors causing sterility in the hybrids. The two species are sympatric and natural hybrids have not been realised.     

Genetic analysis of four self-incompatible lines in Brassica napus

Reciprocal hybridization between four self-incompatible lines of Brassica napus: 271, 181, 184 and ‘White Flower’, revealed incompatibility. The reciprocal F₁s obtained by bud pollination showed self-incompatible reactions, and no segregation for self-incompatibility was observed in all the reciprocal F₂ populations, indicating that lines 271, 181, 184 and ‘White Flower’ were genetically identical with regard to self-incompatibility. Observations of self-incompatibility in 17 hybrids from crosses between line 271 and 17 varieties of B. napus showed 10 of the F₁ hybrids to be self-compatible, while four were partially self-compatible and three were self-incompatible. Genetic analysis based on F₂ and BC₁ populations from five self-compatible F₁ hybrids and two self-incompatible F₁ hybrids suggested the existence of at least two loci controlling the self-incompatibility of line 271: one is the S locus, with dominant and recessive relationships between the S alleles, and the other is the suppressor (sp) of the S locus. The sp locus is genetically different from the S locus, and also shows dominant and recessive relationships between the sp alleles.