Inter-subspecific maps of non-brittle rachis genes btr1/btr2 using occidental, oriental and wild barley lines

Brittle rachis of wild barley is controlled by two dominant complementary genes, Btr1 and Btr2, and mutation in either locus (btr1 or btr2) results in the non-brittle rachis of cultivated barley. In this study, a simple monogenic inheritance of non-brittle rachis was demonstrated, and moreover differentiation of multiple dominant alleles for either Btr1 or Btr2 among cultivated and wild barley lines was suggested. Two amplified-fragment-length polymorphism (AFLP) linkage maps of the genes were constructed using wild × btr1-type cultivar and wild × btr2-type cultivar F₂ populations. The order of AFLPs and the btr1/btr2 locus was constant between the wild × cultivar maps and a cultivar × cultivar map previously constructed. No suppression of recombination due to the inter-subspecific crosses was noticed in the interval studied. The btr1 locus and all AFLP loci were separated in the wild × btr1-type cultivar F₂ map, but the btr2 locus and eight AFLP loci did not recombine in the wild × btr2-type cultivar F₂ map, thus slightly different levels of affinity between parental cultivars with the wild line was suggested at the btr1/btr2 locus.     

Rachis brittleness in a hybrid–parent barley (Hordeum vulgare) breeding germplasm with different combinations at the non-brittle rachis genes

Two dominant, closely linked and complementary genes, Btr1 and Btr2, control rachis brittleness in barley. Recessive mutations in any of these genes turn the fragile rachis (brittle) into a tough rachis phenotype (non-brittle). The cross of parents with alternative mutations in the btr genes leads to a brittle F₁ hybrid that presents grain retention problems. We evaluated rachis fragility through a mechanical test and under natural conditions, in F₁ crosses with different compositions at the btr genes. Brittleness was significantly higher in Btr1btr1Btr2btr2 crosses compared to hybrids and inbred parents carrying one of the mutations (btr1btr1Btr2Btr2/Btr1Btr1btr2btr2). This fact could jeopardize the efficient harvest of hybrids bearing alternative mutations, reducing the choice of possible crosses for hybrid barley breeding and hindering the exploitation of potential heterotic patterns. Furthermore, non-brittle hybrids showed higher brittleness than inbreds, suggesting the presence of other dominant factors affecting the trait. In conclusion, this work encourages a deeper study of the genetic control of the rachis brittleness trait and urges the consideration of rachis tenacity as a target for hybrid barley breeding.     

Means and variances for Fusarium head blight resistance of F2-derived bulks from winter triticale and winter wheat crosses

Fusarium head blight (FHB), caused by Fusarium graminearum and Fusarium culmorum, is a devastating disease in cereals. This study was undertaken to estimate progeny means and variances in each of five winter triticale and winter wheat crosses using unselected F₂−derived lines in F₄ or F₅ generation bulked at harvest of the previous generation. Fifty (triticale) and 95 (wheat) progeny per cross were inoculated in two (triticale) or three (wheat) field environments. FHB rating was assessed on a whole-plot basis. Mean disease severities of the parents ranged from 2.3 to 6.4 in triticale and from 3.1 to 6.5 in wheat on a 1-to-9 scale (1 = symptomless, 9 = 100% infected). The midparent values generally resembled the means of their derived progeny. Significant (P < 0.01) genotypic variance was detected within each cross, but genotype × environment interaction and error variances were also high for both crops. Medium to high entry-mean heritabilities (0.6–0.8) underline the feasibility of selecting F₂-derived bulks on a plot basis in several environments. Phenotypic correlation of FHB resistance between generation F_2:4 and F_2:5 was r = 0.87 (P < 0.01) tested across 150 wheat bulks at two locations. Our estimates of selection gain are encouraging for breeders to improve FHB resistance in triticale and wheat by recurrent selection within adapted materials.     

Inheritance of resistance to two races of sunflower downy mildew (Plasmopara halstedii) in two Helianthus annuus L. lines

Sunflower downy mildew caused by Plasmopara halstedii is an important disease of sunflower capable of causing losses of more than 80% of production. Races 100, 300, 310, 330, 710, 703, 730 and770 of the fungus have been identified in Spain. Race 703, of high virulence, has been identified frequently in the northeast, while race 310 seems to occur over the south, the main sunflower growing region of the country. Oil sunflower lines RHA-274 and DM4 were studied for their resistance to races 310(RHA-274 and DM4) and 703 (DM4). In each cross, only one plant of the resistant parent was crossed to the inbred susceptible line HA-89 (or cmsHA-89).Plants from F₂ and backcross(BC₁F₁ to susceptible parent)generations were evaluated for fungal sporulation on true leaves and/or cotyledons. The resistant-to-susceptible ratios obtained in the F₂ and BC₁F₁ progenies from the crosses cmsHA-89 × RHA-274 and HA-89 × DM4suggested that one major gene in each line is responsible for resistance to race 703.The segregations of the progenies of the cross HA-89 × DM4 inoculated with race 703also fitted the ratios 1:1 and 3:1 (for BC₁F₁ and F₂, respectively)corresponding to control of resistance by a single dominant gene. In RHA-274, the gene for resistance to race 310 was designated Pl ₉, whereas Pl _v is tentatively proposed to designate the gene in DM4 responsible for resistance to races310 and 703. This revised version was published online in August 2006 with corrections to the Cover Date.     

Characterization of segregation distortion on chromosome 3 induced in wide hybridization between indica and japonica type rice varieties

We previously surveyed chromosomal regions showing segregation distortion of RFLP markers in the F₂ population from the cross between a japonica type variety ‘Nipponbare’ and an indica type variety ‘Milyang23’, and showed that the most skewed segregation appeared on the short arm of chromosome 3. By comparison with the marker loci where distortion factors were previously identified, this region was assumed to be a gametophytic selection-2 (ga2) gene region. To evaluate this region, two near isogenic lines (NILs) were developed. One NIL had the ‘Nipponbare’ segment of this region on the genetic background of ‘Milyang23’ (NIL9-23), and the other NIL had the ‘Milyang23’ segment on the genetic background of ‘Nipponbare’ (NIL33-18). NIL9-23 and ‘Milyang23’, NIL33-18 and ‘Nipponbare’, and ‘Nipponbare’ and ‘Milyang23’ were respectively crossed to produce F₁ and F₂ populations. The F₁ plants of NIL9-23 × ‘Milyang23’ and NIL33-18 × ‘Nipponbare’ showed high seed fertility and the same pollen fertility as their parental cultivars, indicating that ga2 does not reduce seed and pollen fertility. Segregation ratio of a molecular marker on the ga2 region in the three F₂ populations was investigated to clarify whether segregation distortion occurred on the different genetic backgrounds. Segregation distortion of the ga2 region appeared in the both F₂ populations from the NIL9-23 and ‘Milyang23’ cross (background was ‘Milyang23’ homozygote) and the ‘Nipponbare’ and ‘Milyang23’ cross (background was heterozygote), but did notin the F₂ population from the NIL33-18 and ‘Nipponbare’ cross (background was ‘Nipponbare’ homozygote). This result indicates that ga2 interacts with a ‘Milyang23’ allele(s) on the different chromosomal region(s) to cause skewed segregation of the ga2 region. In addition, segregation ratio was the same between the F₂ populations from NIL9-23 × ‘Milyang23’ and ‘Nipponbare’ × ‘Milyang23’ crosses, suggesting that the both genotypes, ‘Milyang23’ homozygote and heterozygote, of gene(s) located on the different chromosomal region(s) have the same effect on the segregation distortion. This revised version was published online in July 2006 with corrections to the Cover Date.     

Development of AFLP and derived CAPS markers for root-knot nematode resistance in cotton

Resistance to root-knot nematode (Meloidogyne incognita) is determined by a single major gene rkn1 in Gossypium hirsutum Acala NemX cotton. Bulked segregant analysis (BSA) combined with amplified fragment length polymorphism (AFLP) was used to identify molecular markers linked to rkn1. DNA pools from homozygous susceptible (S) and resistant (R) bulks of an F_2:3 originating from the intraspecific cross NemX × SJ-2 were screened with 128 EcoR1/Mse1 primer combinations. Putative AFLP markers were then screened with 60 F_2:7 RIL plants and four AFLP markers were found linked to rkn1. The linkage of AFLP markers to rkn1 was also confirmed in a F₂ population. The closest AFLP marker was converted to a cleaved amplified polymorphic sequence (CAPS) marker (designated GHACC1) by aligning the sequences from both susceptible and resistant parents. GHACC1 linkage to rkn1 was confirmed in the F₂ (1R:3S), F_2:7 RIL (1R:1S) and the backcross population SJ-2 × F₁ (NemX × SJ-2) (1 heterozygous: 1 homozygous). The four AFLP markers, GHACC1 plus two SSR markers (CIR316 and BNL1231) linked to rkn1 from previous work were mapped to intervals of 2.6–14.2 cM from the rkn1 locus, and the genomic region around rkn1 was spanned to about 28.2 cM in the F_2:7 population. The PCR-based GHACC1 and CIR316 markers were tested on 21 nematode resistant and susceptible cotton breeding lines and cultivars. GHACC1 was suitable for nematode resistance screening within G.␣hirsutum, but not G. barbadense, whereas CIR316 was useful in both species, indicating their␣potential for utilization in marker-assisted selection.     

Genetic Variation in the Ability of Detached and Partially Dehydrated Leaves of Rice to Accumulate Abscisic Acid, Measured by Radioimmunoassay

Variation in the ability o) 60 rice (Oryza saliva L.) varieties and three wild species to accumulate abscisic acid (ABA) in response to drought stress, drought-induced ABA accumulation (DIAA), was assessed using a standard detached-leaf lest. The range in DIAA amongst these genotypes was compared with the range amongst F₂ plants and F₆, lines derived from the O. saliva cross ‘IR20’ב63–83’ which were selected through several generations solely on the basis of differences in DIAA. ABA was measured by radioimmunoassay (RIA) or by gas chromatography (GC). DIAA in the 60 varieties was normally distributed with a six-fold range, from 245 to 1580 ng g^?1 FW. Wild species varied two-fold in DIAA, from 375 to 889 ng g^?1 FW. DIAA in F₂ plants from the ‘1R20’ב63–83’ cross was also normally distributed. The extremes of DIAA for the low-ABA and higb-ABA F₆ lines (330 and 1435ng g^?1 FW) were similar to those for the varieties. Measurements by RIA and GC gave similar results. These findings are discussed in the context of producing further sets of closely-related genotypes with similar leaf areas to study the association between DIAA and water-use efficiency.     

Segregation of 12 isozyme genes among doubled haploid lines derived from a japonica x indica cross of rice (Oryza sativa L.)

Summary The segregation of 12 heterozygous isozyme markers was analyzed among F₂ plants and 51 anther culture (AC)-derived lines obtained from the japonica × indica cross of rice, IRAT 177 × Apura. All the lines except two were homozygous products of recombination of the two parental phenotypes. Doubled haploid (DH) lines derived from plants regenerated from the same callus were identical, confirming previously obtained results in rice. Surprisingly, some lines derived from different calli were also identical, suggesting a phenomenon of early callus fragmentation. All these observations at the isozyme level were confirmed by field evaluation. Deviations of segregations from the expected 1 : 1 ratio were observed at 4 loci among the DH lines. Among these, two were also noted among the F₂ plants. The two other distortions, both in favor of the japonica allele, were observed specifically in the AC-derived materials.Although this concerns a small proportion of the genes under study, it suggests that the embryogenic microsporal population does not represent a random gametic array. On the other hand, evaluation of recombination between isozyme genes located on chromosome 6 appears consistent with F₂ data and data previously recorded on the other japonica × indica crosses. The potential use of isozymes in breeding doubled haploids derived from remote crosses in rice is discussed.Abbreviations MCPA = 2-methyl-4-chlorophenoxyacetic acid - IAA = indolacetic acid - AC plant or line = anther culture-derived plant or line - DH line = doubled haploid line     

Allelic relationships of genes controlling number of flowers per axis in chickpea

Genetic variation for number of flowers per axis in chickpea (Cicer arietinum L.) includes single-flower, double-flower, triple-flower and multi-flower traits. A double-flowered (DF) line ICC 4929, a triple-flowered (TF) line IPC 99-18 and a multi-flowered (MF) line JGM 7 were intercrossed in all possible combinations and flowering behavior of parents, F₁s and F₂s was studied to establish allelic relationships, penetrance and expressivity of genes controlling number of flowers per axis in chickpea. The F₁ from ICC 4929 (DF) × IPC 99-18 (TF) cross were double-flowered, whereas F₁ from ICC 4929 (DF) × JGM 7 (MF) and IPC 99-18 (TF) × JGM 7 (MF) crosses were single-flowered. The F₂ from ICC 4929 (DF) × IPC 99-18 (TF) cross gave a good fit to a 3:1 ratio for double-flowered and triple-flowered plants. The F₂ from ICC 4929 (DF) × JGM 7 (MF) cross segregated in a ratio of 9:3:3:1 for single-flowered, double-flowered, multi-flowered and double-multi-flowered plants. The F₂ from IPC 99-18 (TF) × JGM 7 (MF) cross segregated in a ratio of 9:3:4 for single-flowered, triple-flowered and multi-flowered plants. The results clearly established that two loci control number of flowers per axis in chickpea. The double-flower and triple-flower traits are controlled by a single-locus (Sfl) and the allele for double-flowered trait (sfl ^d ) is dominant over the allele for triple-flower trait (sfl ^t ). The three alleles at the Sfl locus has the dominance relationship Sfl > sfl ^d > sfl ^t . The multi-flower trait is controlled by a different gene (cym). Single-flowered plants have dominant alleles at both the loci (Sfl_ Cym_). The double-flower, the triple-flower and the multi-flower traits showed complete penetrance, but variable expressivity. The expressivity was 96.3% for double-flower and 76.4% for double-pod in ICC 4929, 81.2% for triple-flower and 0.0% for triple-pod in IPC 99-18, and 51.3% for multi-flower and 24.7% for multi-pod in JGM 7. Average number of flowers per axis and average number of pods per axis were higher in JGM 7 than double-flowered line ICC 4929 and triple-flowered line IPC 99-18. The results of this study will help in development of breeding strategies for exploitation of these flowering and podding traits in chickpea improvement.     

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.     

Development and cytogenetic characterisation of a double goat grass-barley chromosome substitution in tritordeum

×Tritordeum (Ascherson et Graebner, an amphiploid between Triticum turgidum conv. durum and Hordeum chilense), and chromosome substitution lines of tritordeum where chromosomes 2 H ^ch or 3 H ^ch H. chilense were replaced with chromosome 2 D of T. aestivum or 3 H ^v chromosome of H. vulgare, respectively, were used to assess the effect of specific chromosomes on the rachis. ×Tritordeum has brittle rachis while the 2 D(2 H ^ch) and 3 H ^v (3 H ^ch) substitution lines have non-brittle rachis. Both lines also have compact spikes, a character highly desirable for the improvement of tritordeum threshability. Different combinations of 2 D and 3 H ^v translocations were developed in tritordeum. In this article we present information on the identification and characterisation of all these introgression lines by the fluorescent in situ hybridisation.     

Identification and validation of a major QTL for salt tolerance in soybean

To identify quantitative trait loci (QTLs) conditioning salt tolerance in soybean (Glycine max (L.) Merr.), two recombinant inbred line (RIL) populations derived from crosses of FT-Abyara × C01 and Jin dou No. 6 × 0197 were used in this study. The FT-Abyara × C01 population consisted of 96 F₇ RILs, and the Jin dou No. 6 × 0197 population included 81 F₆ RILs. The salt tolerant parents FT-Abyara and Jin dou No. 6 were originally from Brazil and China, respectively. The QTL analysis identified a major salt-tolerant QTL in molecular linkage group N, which accounted for 44.0 and 47.1% of the total variation for salt tolerance, in the two populations. In the FT-Abyara × C01 population, three RILs were found to be heterozygous around the detected QTL region. By selfing the three residual heterozygous lines, three sets of near isogenic lines (NILs) for salt tolerance were developed. An evaluation of salt tolerance of the NILs revealed that all the lines with FT-Abyara chromosome segment at the QTL region showed significantly higher salt tolerance than the lines without the FT-Abyara chromosome segment. Results of the NILs validated the salt tolerance QTL detected in the RIL populations.     

Genetics of novel corolla colours in periwinkle

Inheritance of a novel corolla colour in periwinkle [Catharanthus roseus (L) G. Don], viz. magenta, was studied by crossing an accession MJ, possessing this corolla colour, with cultivar Nirmal, possessing white corolla. The accession MJ was also crossed with another accession OR, possessing another novel corolla colour, viz. orange-red, to determine the relationship between genes governing magenta corolla and orange-red corolla. The F₁ plants of the cross MJ× Nirmal had pink corolla and red eye. In the F₂ generation, five kinds of corolla colours were observed: (i) pink corolla and red eye, (ii) rose corolla and red eye, (iii) magenta corolla and red eye, (iv) white corolla and red eye and (v) white corolla. The observed frequencies of the five kinds of plants fitted a ratio of 144:27:9:12:64. The progeny of the backcross, F₁ × MJ, segregated into three kinds of plants, (i) pink corolla and red eye, (ii) rose corolla and red eye and (iii) magenta corolla and red eye, in the ratio of 2:1:1, while the backcross, F₁ × Nirmal, segregated into two kinds of plants, (i) pink corolla and red eye and (ii) white corolla, in the ratio of 1:1. Two new genes (proposed symbols O^m and J) appeared to be involved in the determination of magenta and rose corolla colours. Interaction between four independent genes R, W, O^m and J, appeared to explain the observed segregation in the cross MJ × Nirmal. The F₁ plants of the cross MJ × OR had scarlet-red corolla and red eye. The segregation data of F₂ and backcross generations suggested that genes governing orange-red corolla and magenta corolla were allelic to each other. Two new and non-parental corolla colours viz., rose corolla and scarlet-red corolla, were observed in the progeny of the crosses of the present study.     

The inheritance of quantitative traits in Brassica napus ssp. rapifera (swedes): Augmented triple test cross analyses of production characters

Two F₂ triple test crosses, augmented with F₃s, produced from crosses between different inbred lines of swedes (Brassica napus ssp.rapifera L.) were assessed in field trials at Dundee in 1988 and 1989,respectively. This paper reports the analyses of resistance to powdery mildew, neck length, growth cracks, sugar content and hardness; analyses of yield have been published previously. Additive genetical variation was found for all traits while non-additive variation was less important, the highest degree of dominance being 0.44 for hardness. There was evidence of additive × dominance and dominance × dominance epistasis for mildew and additive × additive epistasis for neck length and hardness. Significant,consistent reciprocal differences were found and these were particularly large for neck length and growth cracks. Sugar determination was carried out on the basic generations of the second cross, the parental lines of which showed large differences in concentration of glucose, fructose and sucrose. Directional dominance was found for high glucose but not for fructose or sucrose. The implications of these results for swede breeding are discussed and it is proposed that inbred cultivars would be a more practical option than F₁ hybrids. This revised version was published online in August 2006 with corrections to the Cover Date.     

A novel source of resistance to the two-spotted spider mite in Lycopersicon pimpinellifolium (Jusl.) Mill.: its genetics as affected by interplot interference

We have previously found an accession of Lycopersicon pimpinellifolium (Jusl.) Mill. (`TO-937') that appeared to resist attack by the two-spotted spider mite (Tetranychus urticae Koch). L. pimpinellifolium is a very close relative of the cultivated tomato (Lycopersicon esculentum Mill.) and thereby a potential source of desirable traits that could be introgressed to the crop species. The objective of this study was to investigate the genetics of the resistance present in `TO-937'. Resistance to infestation by the spider mite was quantified in 24-plant plots of L. pimpinellifolium accessions `TO-937' and `PE-10', L. pennellii accession `PE-45', L. esculentum cultivars `Moneymaker', `Roma' and `Kalohi' (reported to be partially resistant: Stoner & Stringfellow, 1967), and the interspecific F₁ cross, L. esculentum `Moneymaker' × L. pimpinellifolium `TO-937'. Only `TO-937', the F<sub>1</sub>, and`PE-45' were found to be resistant. Resistance of `TO-937' was complete when evaluated in two small greenhouses completely planted with `TO-937' so as to simulate the genotypic homogeneity usual in commercial crops. Generations (P₁, P₂, F₁, F₂, BC₁P₁, and BC₁P₂) of a P₁ (susceptible) × P₂ (resistant) cross (`Moneymaker' × `TO-937') were studied for resistance in a single-plant per plot design. Resistance of `TO-937' was inherited with complete dominance and appeared to be controlled by either two or four genes according to whether segregation in the F₂ or the BC₁P₁, respectively, were considered. However, calculation of the number of genes involved in the resistance was complicated by negative interplot interference due to the high frequency of resistant genotypes within most of the generations. This revised version was published online in July 2006 with corrections to the Cover Date.     

Inheritance of high oleic acid content in safflower

Safflower (Carthamus tinctorius L.) oil with high oleic acid content (>75%) has a great value for both food and non-food uses. The trait has been reported to be environmentally stable and controlled by recessive alleles at one single gene Ol, even though the influence of modifying genes has been suggested. Additionally, germplasm with higher oleic acid content (>85%) has been reported. The objective of the present research was to study the inheritance of high oleic acid content in genetic sources with both levels of high oleic acid content (>75 and >85%, respectively). A genetic study was conducted by crossing the nuclear male-sterile line CL1 (18% oleic acid) and the high oleic acid lines CR-6 (80%) and CR-9 (87%). The evaluation of the F₁ and F₂ seed generations of the crosses CL1 × CR-6 and CL1 × CR-9 indicated that in both cases the high oleic acid trait was controlled by partially recessive alleles at a single locus. The observation of F₂, F₃, and F₄ segregants with high oleic acid phenotype but lower oleic acid levels than the parents revealed the presence of modifying genes affecting the trait. Crosses between the two high oleic acid lines produced no transgressive segregation other than that caused by the mentioned modifying genes, suggesting that the high oleic acid lines CR-6 and CR-9 share the same alleles at the Ol locus. Differences for oleic acid content between both lines were hypothesized to be produced by the accumulation of genes with a minor effect on the trait.     

Variation for aphid resistance and insecticidal acyl sugar expression among and within Lycopersicon pennellii-derived inbred backcross lines of tomato and their F1 progeny

Five inbred backcross lines (IBL) were selected for higher relative expression of insecticidal acyl sugars (rank average) from an inbred backcross population derived from the cross Lycopersicon esculentum cultivar ‘Peto 84’×Lycopersicon pennellii accession LA716. These five BC₂S₅ IBLs were crossed in a partial diallel design (Method II), and their self and F₁ progeny and three control cultivars were tested at two California field locations in 1996. Counts of potato aphids, Macrosiphum euphorbiae Thomas, on leaves, as a measure of plant infestation, revealed significant general combining ability (GCA) for lower aphid numbers with IBL44 and IBL59; the F₁ hybrid IBL44 × IBL59 had significantly fewer aphids per leaflet than the susceptible cultivar ‘Alta’. GCA for acyl sugars was associated with IBL59 only. Of all the IBL and IBL × IBL F₁ hybrids, only IBL59 produced significant levels of acyl sugars. Significant within IBL59 variation for acyl sugars was observed, but not for aphid resistance. Our results suggest that factors other than acyl sugars contributed to L. pennellii-derived aphid resistance in IBL × IBL F₁ hybrids and IBL that do not produce significant amounts of acyl sugars. IBL59 and IBL44 may be useful for breeding for aphid resistance in cultivated tomato.     

Genetic basis of seedling-resistance to leaf rust in bread wheat 'Thatcher'

The bread wheat cultivar ‘Thatcher’ is documented to carry the gene Lr22b for adult‐plant resistance to leaf rust. Seedling‐resistance to leaf rust caused by Puccinia triticina in the bread wheat cultivar ‘Thatcher’, the background parent of the near‐isogenic lines for leaf rust resistance genes in wheat, is rare and no published information could be found on its genetic basis. The F₂ and F₃ analysis of the cross ‘Agra Local’ (susceptible) × ‘Thatcher’ showed that an apparently incompletely dominant gene conditioned seedling‐resistance in ‘Thatcher’ to the three ‘Thatcher’‐avirulent Indian leaf rust pathotypes – 0R8, 0R8‐1 and 0R9. Test of allelism revealed that this gene (temporarily designated LrKr1) was derived from ‘Kanred’, one of the parents of ‘Thatcher’. Absence of any susceptible F₂ segregants in a ‘Thatcher’ × ‘Marquis’ cross confirmed that an additional gene (temporarily designated LrMq1) derived from ‘Marquis’, another parent of ‘Thatcher’, was effective against pathotype 0R9 alone. These two genes as well as a second gene in ‘Kanred’ (temporarily designated LrKr2), which was effective against all the three pathotypes, but has not been inherited by ‘Thatcher’, seem to be novel, undocumented leaf rust resistance genes.     

A new powdery mildew resistance gene: Introgression from wild emmer into common wheat and RFLP-based mapping

An Israeli accession (TTD140) of wild emmer, Triticum turgidum var. dicoccoides, was found resistant to several races of powdery mildew. Inoculation of the chromosome-arm substitution lines (CASLs) of TTD140, in the background of the Israeli common wheat cultivar ‘Bethlehem’ (BL), with five isolates of powdery mildew revealed that only the line carrying the short arm of chromosome 2B of wild emmer (CASL 2BS) exhibited complete resistance to four of the five isolates. To map and tag the powdery mildew resistance gene, 41 recombinant substitution lines, derived from a cross between BL and CASL 2BS, were used to construct a linkage map at the gene region. The map, which encompasses 69.5 cM of the distal region of chromosome arm 2BS, contains six RFLP markers, a morphological marker (glaucousness inhibitor, W1 ^I), and the powdery mildew resistance gene. Segregation ratios for resistance in F₂ of BL × CASL 2BS and in the recombinant lines, combined with the susceptability of F₁ progeny to all tested isolates, indicate that resistance is controlled by a single recessive allele. This alleleco-segregated with a polymorphic locus detected by the DNA marker Xwg516, 49.4 cM from the terminal marker Xcdo456. The new powdery mildew resistance gene was designated Pm26. This revised version was published online in July 2006 with corrections to the Cover Date.     

Identification of alleles at two loci controlling resistance to Phomopsis stem blight in narrow-leafed lupin (Lupinus angustifolius L.)

The genetics of resistance to Phomopsis stem blight caused by Diaporthe toxica Will., Highet, Gams & Sivasith. in narrow-leafed lupin (Lupinus angustifolius L.) was studied in crosses between resistant cv. Merrit, very resistant breeding line 75A:258 and susceptible cv. Unicrop. A non-destructive glasshouse infection test was developed to assess resistance in the F₁, F₂, selected F₂-derived F₃ (F_2:3) families, and in selfed parent plants. The F₁ of Unicrop × 75A:258 (and reciprocal cross) was very resistant, and the F₂ segregated in a ratio of 3:1 (resistant: susceptible), which suggested the presence of a single dominant allele for resistance in 75A:258. In Merrit × Unicrop (and reciprocal), the F₁ was moderately resistant, and the F₂ segregated in a ratio of 3:1 (resistant: susceptible). Thus Merrit appeared to carry an incompletely dominant resistance allele for resistance. The F₁ of Merrit × 75A:258 (and reciprocal) was very resistant and the F₂ segregated in a ratio of 15:1 (resistant: susceptible), which supported the existence of independently segregating resistance alleles for resistance in 75A:258 and Merrit. Alleles at loci for early flowering (Ku) and speckled seeds (for which we propose the symbol Spk) segregated normally and independently of the resistance alleles. Resistant F₂ plants gave rise to uniformly resistant or segregating F_2:3 families, whereas susceptible F₂ plants gave rise only to susceptible F_2:3 families. However, the variation in resistance in the F₂ and some F_2:3 families of crosses involving 75A:258, from moderately to extremely resistant, was greater than that expected by chance or environmental variation. We propose the symbols Phr1 to describe the dominant resistance allele in 75A:258, and Phr2 for the incompletely dominant resistance allele in Merrit. Phr1 appears to be epistatic to Phr2, and expression of Phr1 may be altered by independently segregating modifier allele(s). This revised version was published online in July 2006 with corrections to the Cover Date.