Introgression of hexaploid sources of crown rot resistance into durum wheat

Triticum turgidum ssp. durum (tetraploid durum) germplasm is very susceptible to crown rot, caused by the fungus Fusarium pseudograminearum. Screening activities to date have failed to identify even moderately susceptible lines. In contrast partial resistance to this disease has been identified in a number of Triticum aestivum (hexaploid wheat) lines, including 2-49 and Sunco. This study describes the successful introgression of partial crown rot resistance from each of these two hexaploid wheat lines into a durum wheat background. Durum backcross populations were produced from two 2-49/durum F₆ lines which did not contain any D-genome chromosomes and which had crown rot scores similar to 2-49. F₂ progeny of these backcross populations included lines with field based resistance to crown rot superior to that of the parent hexaploid wheat.     

Conferring resistance to pre-harvest sprouting in durum wheat by a QTL identified in <Emphasis Type="Italic">Triticum spelta</Emphasis>

Pre-harvest sprouting (PHS) causes significant yield loss and degrade the end-use quality of wheat, especially in regions with prolonged wet weather during the harvesting season. Unfortunately, the gene pool of Triticum durum (tetraploid durum wheat) has narrow genetic base for PHS resistance. Therefore, finding out new genetic resources from other wheat species to develop PHS resistance in durum wheat is of importance. A major PHS resistance QTL, Qphs.sicau-3B.1, was mapped on chromosome 3BL in a recombinant inbred line population derived from ‘CSCR6’ (Triticum spelta), a PHS resistant hexaploid wheat and ‘Lang’, a PHS susceptible Australian hexaploid wheat cultivar. This QTL, Qphs.sicau-3B.1, is positioned between DArT marker wPt-3107 and wPt-6785. Two SCAR markers (Ph3B.1 and Ph3B.2) were developed to track this major QTL and were used to assay a BC₂F₈ tetraploid population derived from a cross between the durum wheat ‘Bellaroi’ (PHS susceptible) and ‘CSCR6’ (PHS resistant). Phenotypic assay and marker-assisted selection revealed five stable tetraploid lines were highly PHS resistant. This study has successfully established that PHS-resistance QTL from hexaploid wheat could be efficiently introgressed into tetraploid durum wheat. This tetraploid wheat germplasm could be useful in developing PHS resistant durum cultivars with higher yield and good end-use quality.     

The introduction into bread wheat of a major gene for resistance to powdery mildew from wild emmer wheat

Summary A new source of resistance to wheat powdery mildew caused by Erysiphe graminis has been transferred to hexaploid bread wheat, Triticum aestivum, from the wild tetraploid wheat, Triticum dicoccoides. The donor was crossed to bread wheat and the pentaploid progeny was then self-pollinated. Plants having a near stable hexaploid chromosome complement were selected in the F₃ progeny and topcrossing and backcrossing of these to a second wheat cultivar to improve the phenotype was undertaken. Monosomic analysis of early backcross lines showed the transferred gene to be located on chromosome 4A. The gene has been designated Pm16.     

Development of near-isogenic lines for a major QTL on 3BL conferring Fusarium crown rot resistance in hexaploid wheat

By essentially fixing the genetic background, near-isogenic lines (NILs) are ideal for studies of the function of specific loci. We report in this paper the development of NILs for a major QTL located on the long arm of chromosome 3B conferring Fusarium crown rot (FCR) resistance in hexaploid wheat. These NILs were generated based on the method of the heterogeneous inbred family analysis. 13 heterozygous lines were initially selected from three segregating populations using a single SSR marker linked with the major FCR QTL. The two isolines for each of the putative NILs obtained showed no obvious morphological differences, but differences among the NIL pairs were large. Significant differences in FCR resistance between the isolines were detected for nine of the 13 putative NIL pairs. The presence of the FCR allele from the resistant parent reduced FCR severity by 29.3–63.9% with an average of 45.2% across these NILs. These NILs will be invaluable in further characterising this major FCR locus, in studying the mechanism of FCR resistance and in investigating possible interactions between FCR resistance and other traits of agronomic importance.     

Microsatellite monitoring of recombination around the Vrn-B1 locus of wheat during early backcross breeding

The length of chromosomal segments retained around the Vrn‐B1 gene controlling sensitivity to vernalization in wheat (Triticum aestivum L.) was studied in the first and third backcrosses by using microsatellite markers. Eleven polymorphic markers located on chromosome 5B were used for microsatellite analysis. It was shown in the first backcross that plants with a donor segment around the gene of interest not longer than 50% of chromosome 5B could be selected. When selection is not molecular‐marker assisted, the length of the chromosomal donor segment with the target gene may reach 94% of chromosome 5B even in plants of the third backcross generation. The considerable length differences in the 5B microsatellite loci between the winter and spring lines of wheat studied indicate that these markers are promising in marker‐assisted backcrossing or marker‐assisted selection for the Vrn‐B1 gene using different combinations of Spring and Winter genotypes.     

New durum wheat with Hessian fly resistance from Triticum araraticum and T. carthlicum in Morocco

Hessian fly is an important pest of wheat on the North American continent and the temperate Mediterranean drylands. Yield losses caused by this insect in Morocco are the heaviest in the Mediterranean region and are estimated to be 36% on average. Genetic resistance to Mediterranean Hessian fly biotypes has not been found in durum wheat, although large numbers of durum accessions were screened. Genes for resistance were found in common wheat; some of which are transferable to durum. However, there is a need to broaden the genetic base for resistance in durum wheat. The objective of this work was to introgress resistance from selected Triticum araraticum and T. carthlicum accessions using multiple backcross methodology. The experimental recipient durum wheat included numerous adapted and high‐yielding lines. Testing for Hessian fly resistance under controlled conditions and field yield data showed that this programme yields Hessian fly‐resistant durum lines with good yields and adaptation.     

Resistance to Fusarium crown rot in wheat and barley: a review

Fusarium crown rot (FCR) is becoming a major disease in many parts of the cereal‐growing regions worldwide. Significant QTL conferring FCR resistance have been reported on 13 of the 21 possible hexaploid wheat chromosomes in wheat and on three of the seven chromosomes in barley. Available results show that host resistance to FCR is not pathogen species‐specific, that resistance QTL have strong additive effect and that both plant height and growth rate affect FCR severity. Further, different loci seem to be responsible for resistances to FCR and Fusarium head blight although both diseases can be caused by the same Fusarium pathogens. Although marker‐assisted selection for FCR resistance has been initiated, the available markers are all derived from QTL mapping, which provides only limited resolution. Further work has to be conducted in developing diagnostic markers before significant progress can be made in deploying marker‐assisted selection as a routine tool to accelerate and improve FCR in breeding programmes.     

川麦42遗传背景中人工合成小麦导入位点的SSR标记检测

硬粒小麦和节节麦是六倍体普通小麦的二级基因源,六倍体人工合成小麦遗传变异丰富、蕴藏着丰富的抗性基因,可供现代小麦改良利用。利用人工合成小麦基因资源与四川小麦杂交、回交,已育成了高产、优质、抗病小麦新品种“川麦42”。本文利用217对微卫星（SSR）引物检测“川麦42”遗传背景中人工合成小麦的导入位点,发现24个位点来源于人工合成小麦,占所用引物数的11.06%,远小于理论值25%。川麦42遗传背景中人工合成小麦导入位点在A、B和D染色体组分布频率不均衡,D组>B组>A组;人工合成小麦导入位点在川麦42各染色体间差异也很大,在1B、2B和5A染色体上分布较集中、片段较长,而在1A等11条染色体上则无导入位点;表明人工合成小麦的遗传位点并不按孟德尔遗传规律传至后代,人工选择压力导致遗传位点很大的偏分离行为。     

Chromosome location of genes affecting polyphenol oxidase activity in seeds of common and durum wheat

This study used cytogenetic stocks to investigate the chromosomal location of genes responsible for polyphenol oxidase (PPO) activity in common and durum wheat seeds. Substitution lines of chromosome 2A of hexaploid varieties ‘Cheyenne’, ‘Thatcher’ and ‘Timstein’ in ‘Chinese Spring’ showed significantly higher PPO activity than all other substitution lines of the same variety, with the exception of substitutions of ‘Cheyenne’ chromosome 3A and ‘Thatcher’ chromosome 4B. Substitution lines of chromosome 2A of Triticum turgidum var. dicoccoides and of chromosome 2D of ‘Chinese Spring’ into the tetraploid variety ‘Langdon’ showed a significant increase in PPO activity relative to all other substitution lines in Langdon. The gene(s) responsible for high PPO activity in chromosome 2D from ‘Chinese Spring’ was mapped on the long arm within a deletion that represents 24% of the distal part of the arm. This study shows that genes located in homoeologous group 2 play a major role in the activity of PPO in wheat.     

Suppression/expression of resistance to stripe rust in synthetic hexaploid wheat (Triticum turgidum×T. tauschii)

Seventy-four hexaploid wheats, synthesized by either crossing resistantTriticum turgidum L. var.durum with susceptible/intermediateT. tauschii or susceptible/intermediateT. turgidum with resistantT. tauschii, and their parents were evaluated as seedlings in the greenhouse and as adult-plants at two field locations in Mexico for resistance to pathotype 14E14 of stripe (or yellow) rust (caused byPuccinia striiformis Westend). The seedlings of different synthetic hexaploids showed high phenotypic diversity for resistance. However, the resistance level of only 15 of the 74 synthetic hexaploid wheats were similar to the low infection types of the respective donor parents. The remaining synthetic wheats displayed either intermediate or high infection types. A similar result was also obtained in field tests, where only 18 synthetic hexaploids were resistant as adult-plants. In general, genotypes with seedling resistance were also resistant as adult-plants. A few synthetic hexaploids, which displayed intermediate or susceptible infection types as seedlings were resistant as adult-plants, indicating that additional genes for adult-plant resistance were also present. The fact that resistance of some donor parents was not expressed, or only partially expressed, in a synthetic hexaploid background suggests the presence of suppressor genes in the both the A or B, and D genomes ofT. turgidum andT. tauschii, respectively. The resistance of a donor parent was expressed in a synthetic hexaploid only if the corresponding suppressor was absent in the second parent. Moreover, the suppressors appeared to be resistance gene specific.     

Quality studies in wheat

Summary Eleven wheat lines were derived by five backcrossings and five selfings with Thatcher as the recurrent and Selkirk as the donor parent during backcrossings. The lines and parents were subjected to mixogram and loaf volume studies.Out of eleven backcross lines five were similar to Thatcher, two needed longer mixing time and four were less elastic than Thatcher.Eight of eleven backcross lines had similar loaf volume profiles and two lines were, to a certain extent, similar to Thatcher in loaf volume. One line was quite different from and definitely inferior to Thatcher.It is suggested that the backcross method is a useful tool in quality breeding. In view of the fact that a backcross line with a quality quite different from the recurrent parent may appear in the population, quality evaluation at pre-release stage is strongly advocated.     

Chromosomal location of resistance to Septoria tritici in seedlings of a synthetic hexaploid wheat, Triticum spelta and two cultivars of Triticum aestivum

Chromosomal location of resistance to two virulent Argentinean isolatesof Septoria tritici was studied in two wheat (Triticum aestivumL.) cultivars (Cappelle-Desprez & Cheyenne), a synthetic hexaploid(Synthetic 6x) and Triticum spelta in seedlings. Substitution lines of these(resistant or moderately resistant) genotypes into (susceptible) ChineseSpring were selected from a previous screening. For Synthetic 6x,resistance was clearly located in chromosome 7D. Chinese Spring with the7D chromosome substituted by Synthetic 6x showed almost completeresistance, similar to the level of Synthetic 6x. For the substitutions withCappelle-Desprez, Cheyenne, and T.spelta there were no lines with abehaviour similar to the resistant parent. However, some substitutions weremore resistant than the susceptible parent suggesting that severalchromosomes could be involved in the resistance of these genotypes toSeptoria leaf blotch.     

Detection of quantitative trait loci for leaf rust resistance in wheat––T. timopheevii/T. tauschii introgression lines

Advanced backcross QTL analysis was used to identify QTLs for seedling and adult plant resistance to leaf rust in introgression lines derived from a cross between the spring wheat cultivar ‘Saratovskaya 29’ and a synthetic allopolyploid wheat (T. timopheevii/T. tauschii). F₂ mapping populations involving two backcross selections (‘BC5’ and ‘BC9’ lines) were genotyped with microsatellite markers. Two significant QTL for adult plant resistance were identified in line ‘BC5’: one on chromosome 2B, but originating from chromosome 2G, explained 31% of the trait variance. The other, derived from T. tauschii and mapped to the short arm of chromosome 2D explained 19% of the trait variance. In the second line, one major seedling and adult plant resistance QTL was identified on chromosome 2B. Both QTL co-located to the same marker interval. Such introgression lines, resulting from the reconstruction of common wheat genome, are of interest both as initial material for breeding and improvement of current cultivars, and as a resource for the study of the interaction and transformation of genomes.     

Inheritance of resistance to the Russian wheat aphid in an Iranian durum wheat line

The Russian wheat aphid (RWA), Diuraphis noxia (Mordvilko), is a major economic pest of small grains in many countries. An experiment was therefore conducted to determine the inheritance of gene(s) controlling resistance to RWA in a resistant tetraploid durum wheat line. This resistant line,‘1881′, was crossed to a susceptible line, ‘Orejy‐e‐Kazeroon’, and then F₁ F₂ and BCF₁ (backcross to susceptible line) seedlings were screened in a greenhouse for RWA resistance following artificial infection. Resistance in ‘1881’ was apparently controlled by one dominant gene. Since Dnl, Dn2, dn3, Dn4 and Dn5 have been reported to be located on genome D, it was reasoned that the resistance gene in ‘1881’ is not allelic to them.     

Production of haploids in bread wheat, durum wheat and hexaploid triticale crossed with pearl millet

Pearl millet is an efficient alternative to maize as a pollen source for haploid production in bread wheat. To compare haploid production frequencies in other Triticeae species, the crossabilities of two genotypes each of bread wheat, durum wheat and hexaploid triticale with four pearl millet genotypes and a maize control were examined. Embryos were obtained from crosses of all three species with both pearl millet and maize. However, significant differences in crossability were found among the three species (10.5–79.8% seed development and 1.4–15.8% embryo formation), as well as among genotypes of durum wheat (7.2–23.7% and 2.1–6.4%) and hexaploid triticale (0.3–20.6% and 0.1–2.7%). Crossability of bread wheat with pearl millet was relatively high. Haploid plants were regenerated from crosses of all three species with pearl millet. As in the case of maize crosses, low crossabilities of durum wheat and hexaploid triticale with pearl millet can be attributed to the absence of D-genome chromosomes.     

Location of genes for common bunt resistance in the European winter wheat cv. Trintella

The location of new genes for resistance to common bunt in wheat is valuable for gene pyramiding in breeding. For this purpose, the genetics of the relatively high level of resistance in the European winter wheat variety Trintella was investigated using a doubled haploid mapping population of a cross between Trintella and the susceptible variety Piko. The population was scored for bunt infection in the field for 2 years following inoculation with a mixture of teliospores of Tilletia tritici and T. laevis. A genetic map consisting of 29 linkage groups was constructed using polymorphic simple sequence repeat markers. This map was used for QTL analysis, and in both years, results indicated that resistance to common bunt could mostly be attributed to a gene on chromosome 1B, near to the centromere and closest to marker Xgwm273 on the short arm. Additionally, in 2008, smaller QTL effects were ascribed to chromosomes 7A and 7B, and another smaller QTL effect to chromosome 5B in 2009 only.     

Transfer of disease resistance genes from Triticum araraticum to common wheat

The wild tetraploid wheat species Tr$$ (Zhuk) Zhuk Var. araratieum is a source of pest resistance genes for T$$ aesti$$ L. Our objectives were to describe the breeding behaviour of T.arartuititm when backcrossed to common wheat and transfer resistance to leaf rust (caused by Pu$$) and powdery mildew (caused by Blumeria $$wheat. Crosses were made between five wheat genotypes and $$ accessions. Fertifity and chromosome numbers of BC$$_; plants were determined. Resistance to leaf rust was transferred toBC₂ -derived families from 10 different T’ararati$$an accessions. Leaf rust resistance genes in nine T. araratieum accessions can be assigned to at least four loci. Leaf rust resistance transferred from three accessions was inherited in the hexaploid derivatives as a single. $$ gene in each case. Resistance to powdery mildew was also detected in the T. araratie$$ backcross derivatives. Fertile hexaploid derivatives expressing T’araratieum-derived resistance genes can be recovered after two backcrosses to wheat cultivars.     

Screening for zinc efficiency among wheat relatives and their utilisation for alien gene transfer

Genetic diversity for micronutrient efficiency among the most highly adapted and advanced hexaploid and tetraploid wheat cultivars in the world is limited compared with alien species of wheat or rye. Therefore, screening for zinc efficiency was conducted in greenhouse experiments under controlled conditions, and in field trials. Different varieties of hexaploid wheat, hexaploid oats and diploid rye, together with hexaploid and octoploid triticales, wheat-Agropyron, wheat-Aegilops and several wheat-alien chromosome addition series were studied. Considerable differences in zinc efficiency were found between wheat and its relatives. Individual chromosomes of Secale, Agropyron and Haynaldia were found to carry major genes for this character. The transfer of alien chromosome segments was effective, demonstrated using several wheat-rye translocation lines. Alien genetic information was clearly expressed in the wheat genetic background. Further experimental introgressions by chromosome manipulation and marker-aided selection may efficiently contribute to wheat improvement in marginal soils. This revised version was published online in August 2006 with corrections to the Cover Date.     

小麦品种苏麦3号抗赤霉病基因的染色体定位研究

本研究以苏麦3号为染色体供体,一套“中国春”小麦单体系列分别作为受体和轮回母本,连续回交4次,并建立两套独立转育的重复系,对赤霉病抗性进行了染色体定位研究。结果表明,重复系Ⅰ中,苏麦3号染色体2B、3B和6B与赤霉病抗性有关;重复系Ⅱ中,染色体7A、2B、3B和6B与赤霉病抗性有关。由此推断,苏麦3号的抗性基因位于染色体2B、3B和6B上,染色体7A是否具有抗性基因,还有待于进一步证实。2D染色体载有促进赤霉病扩展的感病基因。     

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.