Cytological analyses of hybrids and derivatives of hybrids between durum wheat and Thinopyrum bessarabicum,using multicolour fluorescent GISH*

The wheat progenitors and other wild relatives continue to be important sources of genes for agronomically desirable traits, which can be transferred into durum wheat (Triticum turgidum; 2n = 4x = 28; AABB genomes) cultivars via hybridization. Chromosome pairing in durum × alien species hybrids provides an understanding of genomic relationships, which is useful in planning alien gene introgression strategies. Two durum cultivars, ‘Lloyd’ and ‘Langdon’, were crossed with diploid wheatgrass, Thinopyrum bessarabicum (2n = 2x = 14; JJ), to synthesize F₁ hybrids (2n = 3x = 21; ABJ) with Ph1. ‘Langdon’ disomic substitution 5D(5B) was used as a female parent to produce F₁ hybrids without Ph1, which resulted in elevation of pairing between durum and grass chromosomes – an important feature from the breeding standpoint. The F₁ hybrids were backcrossed to respective parental cultivars and BC₁ progenies were raised. ‘Langdon’ 5D(5B) substitution × Th. bessarabicum F₁ hybrids were crossed with normal ‘Langdon’ to obtain BC₁ progeny. Chromosome pairing relationships were studied in F₁ hybrids and BC₁ progenies using both conventional staining and fluorescent genomic in situ hybridization (fl‐GISH) techniques. Multicolour fl‐GISH was standardized for characterizing the nature and specificity of chromosome pairing: A–B, A–J and B–J pairing. The A–J and B–J pairing will facilitate gene introgression in durum wheat. Multicolour fl‐GISH will help in characterizing alien chromosome segments captured in the durum complement and in their location in the A and/or B genome, thereby accelerating chromosome engineering research.     

QTL mapping of adult‐plant resistance to stripe rust in a ‘Lumai 21 × Jingshuang 16’ wheat population

Stripe rust, caused by Puccinia striiformis f. sp. tritici, is a devastating fungal disease in common wheat (Triticum aestivum L.) worldwide. Chinese wheat cultivars ‘Lumai 21’ and ‘Jingshuang 16’ show moderate levels of adult‐plant resistance (APR) to stripe rust in the field, and they showed a mean maximum disease severity (MDS) ranging from 24 to 56.7% and 26 to 59%, respectively, across different environments. The aim of this study was to identify quantitative trait loci (QTL) for resistance to stripe rust in an F₃ population of 199 lines derived from ‘Lumai 21’ × ‘Jingshuang 16’. The F₃ lines were evaluated for MDS in Qingshui, Gansu province, and Chengdu, Sichuan province, in the 2009–2010 and 2010–2011 cropping seasons. Five QTL for APR were detected on chromosomes 2B (2 QTL), 2DS, 4DL and 5DS based on mean MDS in each environment and averaged values from all three environments. These QTL were designated QYr.caas‐2BS.2, QYr.caas‐2BL.2, QYr.caas‐2DS.2, QYr.caas‐4DL.2 and QYr.caas‐5DS, respectively. QYr.caas‐2DS.2 and QYr.caas‐5DS were detected in all three environments, explaining 2.3–18.2% and 5.1–18.0% of the phenotypic variance, respectively. In addition, QYr.caas‐2BS.2 and QYr.caas‐2BL.2 colocated with QTL for powdery mildew resistance reported in a previous study. These APR genes and their linked molecular markers are potentially useful for improving stripe rust and powdery mildew resistances in wheat breeding.     

Characterization of wheat-triticale doubled haploid lines by cytological and biochemical markers

Five wheat-triticale doubled haploid (DH) lines— M08, V209, DH220-14-2, DH696-3-4 and M16 —derived from anther culture of F₁s resulting from crosses involving hexaploid or octoploid triticale × hexaploid wheat, were characterized by cytological and biochemical markers. Cytological evidence from genomic in situ hybridization and C-banding indicated that DH lines M08 and V209 (2n= 42) each contained a pair of 1BL/1RS translocation chromosomes. DH220-14-2 (2n= 42) was also a translocated line with two pairs of chromosomes containing small fragments of rye. One of the translocation fragments carried the Sec-1R gene originating from the satellite region of 1RS; the origin of the other one remains unknown. DH696-3-4 (2n= 42) contained a 3D(3R) substitution. In M16 (2n= 44), three pairs of rye chromosomes, 3R, 4R and 6R, were present, 4R as an addition and 3D(3R) and 6D(6R) as substitutions. Biochemical, isozyme and storage protein markers confirmed the cytological conclusions. The advantages of transferring alien chromosomes or chromosome fragments into wheat and creating alien aneuploid lines by anther culture of hybrid F¹s are discussed.     

Cytogenetic analysis of a spontaneous 5B/6B translocation in tetraploid wheat landraces from Ethiopia, and implications for breeding

Three tetraploid (2n= 4x= 28) wheat Triticum turgidum L. landrace morphotypes (= genotypes) from Ethiopia were found to carry a variant karyotype directly discernible under the microscope. This was possible because the rearrangement involved one of the satellited chromosomes. Giemsa C-banding revealed that the rearrangement resulted from a 5BS.6BS(5BL.6BL) centric reciprocal translation. The banding pattern on 5BL was polymorphic, suggesting that this translocation might have occurred more than once. There was little C-band polymorphism for the remaining chromosomes, except for 2A. As pure lines, all three morphotypes showed normal chromosome pairing at metaphase I (MI) in pollen mother cells (PMCs). indicating that they are genomically stable. Meiotic analyses of F₁ hybrids and F₂ segregates derived from crosses with tester varieties clearly indicated that one of them (B-l–9) carried another translocation. However, we were not successful in delecting the chromosomes involved, presumably the interchanged segments did nol include C-banding regions. By using T5BS.6BS, direct evidence for segregation distortion against translocation homozygotes in intervarietal hybrids was obtained. The distorted segregation was attributed lo zygotic selection. No aneuploid plants were obtained from the F₂ segregates. However, translocation heterozygotes resulting in unstable meiosis were abundant in the F₂ generation. The implications of the results in using the indigenous landraces in hybridization breeding are discussed.     

Introgression of useful genes from Thinopyrum intermedium to wheat for improvement of bread‐making quality

To study the influence of genes from Thinopyrum intermedium on traits affecting the bread‐making quality of wheat, two derivatives from a putative disomic addition line in cultivar ‘Vilmorin 27’ were used in cytological, biochemical and molecular characterization. Cytological analysis suggested that one of the derivatives (Line‐1) had a terminal deletion involving the long arm of chromosome 1D (2n = 42, Del‐1DL”), and the other (Line‐2) was a conventional addition line, but also carried the same deletion on chromosome 1D (2n = 44, Thi”+Del‐1DL”). Amplification and sequencing of high‐molecular‐weight glutenin subunit (HMW‐GS) genes coded by the Th. intermedium chromosome in Line‐2 indicated the presence of one x‐type with an extra cysteine and four (rather than one) unique y‐type genes. Rheological studies of Line‐1 showed significantly lower dough strength compared to ‘Vilmorin 27’, confirming the recognized role of Glu‐1D coded HMW‐GSs. Line‐2 showed significantly higher dough strength compared to the background cultivar, indicating a significant potential of Th. intermedium for improvement of bread‐making quality in wheat.     

Morphological and cytogenetic studies on the hybrid between bread wheat and <Emphasis Type="Italic">Psathyrostachys huashanica</Emphasis> Keng ex Kuo

Psathyrostachys huashanica Keng ex Kuo (2n = 2x = 14, NsNs), a source of wheat stripe rust, take-all fungus, and powdery mildew resistance with tolerance to salinity and drought, has been successfully hybridized as the pollen parent to bread wheat without using immature embryo rescuing culture for the first time. All of the CSph2b × P. huashanica hybrid seeds germinate well. Backcross derivatives were successfully obtained. F₁ hybrids were verified as intergeneric hybrids on the basis of morphological observation, cytological and molecular analyses. The results obviously showed the phenotypes of the hybrid plants were intermediate between bread wheat and P. huashanica. Chromosome pairing at MI of PMCs in the F₁ hybrid plants was low, and the meiotic configuration was 26.80 I + 0.60 II (rod). Cytological analysis of the hybrid plants revealed the ineffectiveness of the ph2b gene on chromosome association between the parents. Eight RAPD-specific markers for Ns genome were selected for RAPD analysis, and the results indicated that F₁ hybrids contained the Ns genome of P. huashanica. Furthermore, the significance of the finding for bread wheat improvement was discussed.     

Heredity of phenylpropenes in sweet basil (Ocimum basilicum L.) chemotypes and their distribution within an F2 population

Phenylpropenes play an important role in plant defense against animals and microorganisms, and in attracting pollinators and insects. We report the genetic inheritance of methyl chavicol and eugenol following a cross between the sweet basil varieties ‘Perrie’ and ‘Cardinal,’ eugenol and methyl chavicol chemotypes, respectively. Methyl chavicol was detected only in ‘Cardinal,’ accounting for more than 95% of the total phenylpropenes. Eugenol was most abundant in ‘Perrie,’ accounting for more than 99% of the total phenylpropenes. Eugenol, chavicol and methyl chavicol were detected in F₁ hybrids at intermediate levels (10%–52%) without statistical differences (p > .05) for any compound among the F₁ progeny arising from the different crossed pairs. The F₂ progeny segregated into three groups, 23%–25% to a eugenol chemotype, 23%–25% to a methyl chavicol chemotype, and the remaining (~50%) into an intermediate mixture of the two compounds. This distribution fitted a segregation ratio of 1:2:1 (χ² = 1.71; p = .4249), suggesting that the phenylpropene phenotype is regulated by a single bi‐allelic gene with incomplete dominance. A putative association with biosynthesis enzymes is discussed.     

Effect of Rht Alleles on the Tolerance of Wheat Grain Set to High Temperature and Drought Stress During Booting and Anthesis

Factorial pot experiments were conducted to compare the responses of GA‐sensitive and GA‐insensitive reduced height (Rht) alleles in wheat for susceptibility to heat and drought stress during booting and anthesis. Grain set (grains/spikelet) of near‐isogenic lines (NILs) was assessed following three day transfers to controlled environments imposing day temperatures (t) from 20 to 40 °C. Transfers were during booting and/or anthesis and pots maintained at field capacity (FC) or had water withheld. Logistic responses (y = c/1+e^{‐b(t ‐m)}) described declining grain set with increasing t, and t₅ was that fitted to give a 5 % reduction in grain set. Averaged over NIL, t₅ for anthesis at FC was 31.7 ± 0.47 °C (S.E.M., 26 d.f.). Drought at anthesis reduced t₅ by <2 °C. Maintaining FC at booting conferred considerable resistance to high temperatures (t₅ = 33.9 °C) but booting was particularly heat susceptible without water (t₅ = 26.5 °C). In one background (cv. Mercia), for NILs varying at the Rht‐D1 locus, there was progressive reduction in t₅ with dwarfing and reduced gibberellic acid (GA) sensitivity (Rht‐D1a, tall, 32.7 ± 0.72; Rht‐D1b, semi‐dwarf, 29.5 ± 0.85; Rht‐D1c, severe dwarf, 24.2 ± 0.72). This trend was not evident for the Rht‐B1 locus or for Rht‐D1b in an alternative background (Maris Widgeon). The GA‐sensitive severe dwarf Rht12 was more heat tolerant (t₅ = 29.4 ± 0.72) than the similarly statured GA‐insensitive Rht‐D1c. The GA‐sensitive, semidwarfing Rht8 conferred greater drought tolerance in one experiment. Despite the effects of Rht‐D1 alleles in Mercia on stress tolerance, the inconsistency of the effects over background and locus led to the conclusion that semidwarfing with GA‐insensitivity did not necessarily increase sensitivity to stress at booting and flowering. In comparison with effects of semidwarfing alleles, responses to heat stress are much more dramatically affected by water availability and the precise growth stage at which the stress is experienced by the plants.     

Effects of Salinity on Growth, Ionic Relations and Physiological Traits of Wheat, Disomic Addition Lines from Thinopyrum bessarabicum, and Two Amphiploids

The effects of NaCl on the growth, ion relations and physiological characteristics at early stages of growth of bread wheat (Triticum aestivum) varieties ‘Chinese Spring’ and ‘Glennson 81’, ‘Chinese Spring’ lines tetrasomic for chromosomes 5A, 2B and 5B, ‘Chinese Spring’ disomic addition lines for chromosomes 2E^b and 5E^b from Thinopyrum bessarabicum (formerly Agropyron junceum), and amphiploids between ‘Chinese Spring’ and Thinopyrum bessarabicum and ‘Chinese Spring’ and Lophopyrum elongatum (formerly Agropyron elongatum) were examined. Plants were grown in a controlled environment cabinet, in nutrient solution with or without addition of 200 mol m^?3 NaCl. Growth in terms of leaf area, shoot and root weights was reduced by salt treatment. Salinity conditions gradually reduced the osmotic potential, though there was little effect on water potential. Turgor pressure was not much affected by salt. There was variation between genotypes for all the characteristics studied, especially in the extent of Na accumulation by leaves and roots. The amphiploids and 5E^b addition line accumulated the least Na in comparison with other genotypes. Generally roots accumulated lower quantities of Na than leaves. Genotype K contents were not affected by salt treatment. Stomatal conductance also declined whilst the ABA content increased in the salt treated seedlings. With respect to growth, the amphiploids and 5Eb addition line were most tolerant to salt while ‘Glennson 81’, tetrasomic 2B and tetrasomic 5B lines were most susceptible. The addition of homoeologous group 2 and 5 chromosomes reduced the tolerance to salt relative to ‘Chinese Spring’ euploid. It is concluded that chromosome 5E^b of Thinopyrum bessarabicum carries gene(s) for tolerance to salt and this tolerance may be due to the ability to exclude Na ions from the leaves and roots.     

Segregation distortion in common wheat of a segment of Thinopyrum intermedium chromosome 7E carrying Bdv3 and development of a Bdv3 marker

Yellow dwarf (YD) disease is one of the most destructive diseases of cereals worldwide. Wheat (Triticum aestivum L.)–Thinopyrum intermedium 7E(7D) substitution line P29 carries resistance to YD, known as Bdv3, that originates on the long arm of chromosome 7E of Th. intermedium, and the resistance was introgressed into wheat chromosome 7D as T7DS.7DL–7EL in the translocation lines P961341 and P98134. Until now, quantification of YD viruses in cereal crops was usually done by enzyme‐linked immunosorbent assay (ELISA), which is time consuming and laborious. To facilitate this analysis, SSR‐Bdv3, a diagnostic molecular marker, was developed in this study. The transmission of the Th. intermedium segment with Bdv3 was investigated using the SSR‐Bdv3 marker and ELISA in F₂ and testcross progeny derived by crossing two wheat–Th. intermedium translocation lines to four common wheat cultivars. A Th. intermedium chromosome 7E segment in the translocation line P98134 was preferentially transmitted through male gametes in all of its crosses with the four wheat cultivars. However, the transmission frequency of the Th. intermedium 7E segment in another wheat–Th. intermedium translocation line, P961341, varied in different genetic backgrounds. The F₂ populations from reciprocal crosses of Chinese Spring and P961341 showed good fits to the expected ratio of 1 : 2 : 1. In this study, male preferential transmission for either chromosome 7E or chromosome 7D was observed in the progeny derived by crossing P961341 to other wheat cultivars.     

An assessment of the salt tolerance of wheat/Thinopyrum bessarabicum 5Eb addition and substitution lines

Lines of Triticum aestivum cv. Chinese Spring carrying an additional chromosome 5E^b from Thinopyrum bessarabicum or having chromosome 5A or 5D replaced by chromosome 5E^b were screened in hydroculture for tolerance to salt. The previously reported tolerance of the 5E^b addition line was confirmed and the two substitution lines were shown to have a higher level of survival in 175 mol/m³ NaCl than both the addition and the ‘Chinese Spring’ parent. Reasons for the better tolerance of the substitutions are discussed.     

Methodology for creating alloplasmic soybean lines by using Glycine tomentella as a maternal parent

Soybean breeders have not exploited the diversity of the 26 wild perennial species of the subgenus Glycine Willd. that are distantly related to soybean [Glycine max (L.) Merr.] and harbour useful genes. The objective of this study was to develop a methodology for introgressing cytoplasmic and genetic diversity from Glycine tomentella PI 441001 (2n = 78) into cultivated soybean using ‘Dwight’ (2n = 40) as the male parent. Immature seeds (19–21 days post‐pollination) were cultured in vitro to produce F₁ plants (2n = 59). Amphidiploid (2n = 118) plants, induced by colchicine treatment, were vigorous and produced mature pods and seeds after backcrossing with ‘Dwight’. The BC₁ plants (2n = 79) produced mature seeds in crosses with ‘Dwight’. Chromosome numbers in BC₂F₁ plants ranged from 2n = 41–50. From BC₂F₂ to BC₃F₁, the number of plants in parentheses with 2n = 40 (275), 2n = 41 (208), 2n = 42 (80), 2n = 43 (27), 2n = 44 (12) and 2n = 45 (3) were identified. Fertile lines were grown in the field during 2012 and 2013. This is the first report of the successful development of new alloplasmic soybean lines with cytoplasm from G. tomentella.     

Molecular cytogenetic characterization of two partial wheat Elytrigia elongata amphiploids resistant to powdery mildew

Two new partial amphiploids SN20 and SN122, derived from crosses between Elytrigia elongata and common wheat Yannong15 and Shannongfu63, were found resistant to powdery mildew, a serious fungal wheat disease. Cytogenetic observations showed that each SN20 and SN122 plant had 56 chromosomes. The chromosomes in most pollen mother cells formed approximately 28 bivalents, thereby showing a high degree of cytogenetic stability. Genomic in situ hybridization using St‐genomic DNA from Pseudoroegneria strigosa as a probe and ABD‐genomic DNA from Chinese Spring wheat as a blocker demonstrated that the genomic formulas for the alien chromosomes in SN20 and SN122 were 2 St + 10 J^S + 2 J and 2 St + 8 J^S + 4 J, respectively. These wheat E. elongata partial amphiploids represent a potential novel source of resistance to powdery mildew for wheat breeding.     

Genetic mapping and inheritance of Russian wheat aphid resistance gene in accession IG 100695

The Russian wheat aphid (RWA), Diuraphis noxia (Kurdjumov), is an important pest of small‐grain cereals, particularly wheat, worldwide. The most efficient strategy against the RWA is to identify sources of resistance and to introduce them into susceptible wheat genotypes. This study was conducted to determine the mode of inheritance of the RWA resistance found in ICARDA accession IG 100695, to identify wheat microsatellite markers closely linked to the gene and to map the chromosomal location of the gene. Simple sequence repeat (SSR) marker scores were identified in a mapping population of 190 F₂ individuals and compared, while phenotypic screening for resistance was performed in F_2 : 3 families derived from a cross between ‘Basribey’ (susceptible) and IG 100695 (resistant). Phenotypic segregation of leaf chlorosis and rolling displayed the effect of a single dominant gene, temporarily denoted Dn100695, in IG 100695. Dn100695 was mapped on the short arm of chromosome 7D with four linked SSR markers, Xgwm44, Xcfd14, Xcfd46 and Xbarc126. Dn100695 and linked SSR markers may be useful for improving resistance for RWA in wheat breeding.     

Quantitative trait loci mapping of adult‐plant resistance to leaf rust in a Fundulea 900 × ‘Thatcher’ wheat cross

Wheat leaf rust (LR), caused by the obligate biotrophic fungus Puccinia triticina (Pt), is a destructive foliar disease of common wheat (Triticum aestivum L.) worldwide. The most effective, economic means to control the disease is resistant cultivars. The Romanian wheat line Fundulea 900 showed high resistance to LR in the field. To identify the basis of resistance to LR in Fundulea 900, a population of 188 F_2:3 lines from the cross Fundulea 900/‘Thatcher’ was phenotyped for LR severity during the 2010–2011, 2011–2012 and 2012–2013 cropping seasons in the field at Baoding, Hebei Province. Bulked segregant analysis and simple sequence repeat markers were used to identify the quantitative trait loci (QTLs) for LR adult‐plant resistance in the population. Three QTLs were detected and designated as QLr.hebau‐1BL, QLr.hebau‐2DS and QLr.hebau‐7DS. Based on the chromosome positions and molecular marker tests, QLr.hebau‐1BL is Lr46, and QLr.hebau‐7DS is Lr34. QLr.hebau‐2DS was derived from ‘Thatcher’ and was close to Lr22. This result suggests that Lr22b may confer residual resistance on field nurseries when challenged with isolates virulent on Lr22b, or another gene linked to Lr22b confers this resistance from ‘Thatcher’. This study confirms the value of Lr34 and Lr46 in breeding for LR resistance in China; the contribution of the QTL to chromosome 2D needs further validation.     

Blue aleurone trait diagnoses developmental origin of three pistils in a floret in common wheat

The common ‘three‐pistil’ (TP) wheat mutation line expresses TPs in a floret normally containing TPs forming three grains set close back‐to‐back. The developmental origin of the TP trait in common wheat had been diagnosed non‐destructively using the blue aleurone trait. The aleurone colour of F₂ seeds grown in F₁ plants of cross TP/UC66049 was evaluated. Due to xenia, the hue of blue grain colour depended on dose of the Ba1 gene for blue aleurone in the triploid endosperm. The TP trait produced four types of segregation in three‐seed clusters: (i) white grain only, (ii) two white grains and one blue, (iii) one white grain and two blue, and (iv) three blue grains only. The observed frequency of blue–white seed within clusters followed the binominal distribution ₃C_r (0.75)^r·(0.25)^3–r, where r is the number of colour variants in three‐seed clusters (r = 0–3). Intrafloret segregation of seed colour and F₂ segregation derived from aleurone colour of F₃ seeds indicated an independent origin of the TP trait.     

Development and molecular cytogenetic identification of a new wheat–Leymus mollis Lm#6Ns disomic addition line

We developed a new disomic addition line M11028‐1‐1‐5 (2n = 44 = 21” + 1”) from a cross between wheat cv. ‘7182’ and octoploid Tritileymus M47 (2n = 8x = 56, AABBDDN sNs ). Cytological observations demonstrated that M11028‐1‐1‐5 contained 44 chromosomes and formed 22 bivalents during meiotic metaphase I. The genomic in situ hybridization (GISH) investigations showed this line contained 42 wheat chromosomes and a pair of L. mollis chromosomes. SSR, EST and PCR‐based landmark unique gene (PLUG) markers were screened to determine the homoeologous relationships of the introduced L. mollis chromosomes in wheat background. Nine markers, i.e. Xwmc256, Xgpw312, Swes123, CD452568, BF483643, BQ169205, TNAC1748, TNAC1751 and TNAC1752, all of which were located on the homoeologous group 6 chromosomes of common wheat, amplified bands unique to L. mollis in M11028‐1‐1‐5. Gliadin analysis also confirmed that the added chromosomes in M11028‐1‐1‐5 were correlated with the sixth group chromosome. This indicated that M11028‐1‐1‐5 contained a pair of introduced L. mollis chromosome belonging to homoeologous group 6, which we designated it as Lm#6 Ns disomic addition line. This is the first report of a common wheat–L. mollis disomic addition line.     

Heterosis and heritability in crosses among Asian and Ethiopian parents of hot pepper genotypes

Hot pepper is the most important worldwide grown and consumed spice and vegetable crop. Though hybrid breeding has been proposed for genetic improvement in the crop, but there is lack of information on heterosis in crosses among crop genotypes in Ethiopia. Twelve genotypes (nine Asian and three Ethiopian parents) of hot pepper were crossed in 2003 cropping season in a half-diallel fashion to fit Griffing’s fixed effect model analysis. An open field experiment was conducted in 2004/2005 to investigate heterosis for fourteen traits in 66 F₁ hybrids grown together with their 12 selfed parents. Highly significant genotypic differences were observed for all the traits except for leaf area. Variance component due to specific combining ability (dominance) were larger than that due to general combining ability (additive) for each of the studied traits with few exceptions. Broad sense heritability (H _b²) for fruit traits were more than 60% and with wide gap from narrow sense heritability (h _n²) for most of the important traits like number of fruit per plant (H _b² = 88.3% and h _n² = 46.0%), days to maturity (H _b² = 87.2% and h _n² = 23.1%) and dry fruit yield per plant (H _b² = 72.6% and h _n² = 14.6%). Maximum heterosis over mid-parent and better-parent, and economic superiority of hybrid over standard check were recorded, respectively for dry fruit yield per plant (163.8, 161.8 and 92.1%), number of fruits per plant (104.4, 79.6 and 136.4%) and days to maturity (−29.8, −31.5 and −23.6%). These observations suggested a possibility of utilizing dominance genetic potentiality available in diverse genotypes of the crop by heterosis breeding for improving hot pepper to the extent of better economic return compared to the current commercial cultivar under production in the country. Low narrow sense versus very high broad sense heritability for days to maturity and dry fruit yield per plant could be a sign for achievability of earliness and high fruit yield using heterosis in hot pepper. The maximum heterobeltiosis were recorded either from F₁s obtained from Ethiopian and Asian crosses or from within Asian crosses, suggesting the possibility of maximizing heterosis by considering genetically diverse parental genotypes. The manifestation of highest heterosis in hybrids from among Asian lines indicated existence of genetic diversity among Asian genotypes and the potentiality for improvement of hot pepper using genotypes from different regions of the world along with elite inbred lines from local cultivars.     

Development and characterization of two new <Emphasis Type="Italic">Triticum aestivum</Emphasis>–<Emphasis Type="Italic">Dasypyrum</Emphasis><Emphasis Type="Italic">villosum</Emphasis> Robertsonian translocation lines T1DS·1V#3L and T1DL·1V#3S and their effect on grain quality

Dasypyrum villosum (L.) Candargy is a diploid, wild relative of bread wheat (Triticum aestivum L.). Previous studies showed that D. villosum chromosome 1V has genes that encode seed storage proteins that may be used to enhance the grain quality of bread wheat. As a first step in genetic transfer, the present study was initiated to develop compensating Robertsonian translocations involving wheat chromosome 1D and D. villosum chromosome 1V and to analyze their effects on grain quality. A monosomic 1D stock was crossed with the disomic addition stock DA1V#3 and the double monosomic plants (20″ + 1D′ + 1V#3′) were self pollinated. Two co-dominant STS markers (BE499250 and BE591682) polymorphic for the short arm of 1V#3S and two dominant STS markers (BE518358 and BE585781) polymorphic for the long arm of 1V#3L were developed to screen a large number of progeny to identify plants that had only the 1V#3S or 1V#3L arms. Five compensating Robertsonian heterozygous translocations, two (plants #56 and #83) for the short arm (T1DL·1V#3S) and three (plants #7, #123, and #208) for the long arm (T1DS·1V#3L) were identified from 282 F₂ plants and confirmed by genomic in situ hybridization and C-banding analyses. Two homozygous translocations T1DL·1V#3S (plants #14 and #39) were identified from 52 F₃ plants derived from F₂ plant #83. Four homozygous translocations T1DS·1V#3L (plants #3, #22, #29, and #30) were identified from 68 F₃ plants derived from F₂ plant #208. The homozygous translocation T1DL·1V#3S had a significantly higher (37.4 ml) and T1DS·1V#3L had significantly lower (10 ml) Zeleny sedimentation values compared to Chinese Spring wheat (30.7 ml). Our results showed that 1V#3S increased gluten strength and enhanced wheat quality, but 1V#3L decreased gluten strength and did not enhance wheat quality.     

Mapping the <Emphasis Type="Italic">compactum</Emphasis> locus in wheat (<Emphasis Type="Italic">Triticum aestivum</Emphasis> L.) and its relationship to other spike morphology genes of the Triticeae

The spikes of club wheat are significantly more compact than spikes of common wheat due to the action of the dominant allele of the compactum (C) locus. Little is known about the location of C on chromosome 2D and the relationship between C and to other spike-compacting genes. Thus, a study was undertaken to place C on linkage maps and a chromosome deletion bin, and to assess its relatedness to the spike compacting genes zeocriton (Zeo) from barley and soft glume (Sog) from T. monococcum. Genetic mapping was based on recombinant inbred lines (RILs) from a cross between the cultivars Coda (club) and Brundage (common) and F₂ progeny from a cross between the club wheat Corrigin and a chromosome 2D substitution line [Chinese Spring (Ae. tauschii 2D)]. The C locus was flanked by Xwmc144 and Xwmc18 in the RIL population and it was completely linked to Xcfd116, Xgwm358 and Xcfd17 in the F₂ population. C could not be unambiguously placed to a chromosome bin because markers that were completely linked to C or flanked this locus were localized to chromosome bins on either side of the centromere (C-2DS1 and C-2DL3). Since C has been cytogenetically mapped to the long arm of chromosome 2D, we suspect C is located in bin C-2DL3. Comparative mapping suggested that C and Sog were present in homoeologous regions on chromosomes 2D and 2A^m, respectively. On the other hand, C and Zeo, on chromosome 2H, did not appear to be orthologous.