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The genetic diversity of common wheat hybrid lines Triticum aestivum/ Triticum durum and Triticum aestivum/ Triticum dicoccum (2 n = 42, F) using chromosome-specific microsatellite (SSR) markers and C-banding of chromosomes was studied. Cluster analysis of data obtained by 42 SSR markers indicated that the hybrid lines can be broken into three groups according to their origin. There were two cases of complete genetic similarity between lines 183-2/184-6 and 208-3/213-1, which were obtained using common wheat as the parental plants. In cross combinations, when the stabilization of the nuclear genome of hexaploid lines occurred against a background of the cytoplasmic genome of tetraploid wheats, there was a high level of divergence between sister lines, in some cases exceeding 50%. The evaluation of the degree of susceptibility of the lines to powdery mildew, leaf and stem rust, and septoria leaf blotch was performed under different environmental conditions. It was shown that resistance to powdery mildew and leaf rust significantly depended on the region where assays were conducted. An evaluation of the field data showed that the lines 195-3, 196-1, and 221-1 with T. durum genetic material displayed complex resistance to fungal pathogens in Western Siberia and the Republic of Belarus. For lines 195-3 and 196-1, one shows a possible contribution of chromosomes 4B and 5B in the formation of complex resistance to diseases. Hybrid lines with complex resistance can be used to expand the genetic diversity of modern common wheat cultivars for genes of immunity. [ABSTRACT FROM AUTHOR]

Spot blotch caused by Bipolaris sorokiniana is a destructive disease of wheat in warm and humid wheat growing regions of the world. To identify quantitative trait loci (QTLs) for spot blotch resistance, two mapping populations were developed by making the crosses between common susceptible cultivar 'Sonalika' with the resistant breeding lines 'Ning 8201' and 'Chirya 3'. Single seed descent derived F, F, F lines of the first cross 'Ning 8201' × 'Sonalika' were evaluated for resistance to spot blotch in three blocks in each of the 3 years. After screening of 388 pairs of simple sequence repeat primers between the two parents, 119 polymorphic markers were used to genotype the mapping population. Four QTLs were identified on the chromosomes 2AS, 2BS, 5BL and 7DS and explained 62.9% of phenotypic variation in a simultaneous fit. The QTL on chromosome 2A was detected only in 1 year and explained 22.7% of phenotypic variation. In the second cross ('Chirya 3' × 'Sonalika'), F and F population were evaluated in three blocks in each of the 2 years. In this population, five QTLs were identified on chromosomes 2BS, 2DS, 3BS, 7BS and 7DS. The QTLs identified in the 'Chirya 3' × 'Sonalika' population explained 43.4% of phenotypic variation in a simultaneous fit. The alleles for reduced disease severity in both the populations were derived from the respective resistant parent. The QTLs QSb.bhu-2B and QSb.bhu-7D from both populations were placed in the same deletion bins, 2BS1-0.53-0.75 and 7DS5-0.36-0.61, respectively. The closely linked markers Xgwm148 to the QTL on chromosome 2B and Xgwm111 to the QTL on chromosome 7D are potentially diagnostic markers for spot blotch resistance. [ABSTRACT FROM AUTHOR]

Introgressive lines resulting from crossing common wheat Triticum aestivum with the tetraploid T. timopheevii are characterized by effective resistance to leaf rust caused by Puccinia triticina Eriks. Molecular analysis using 350 specific simple sequence repeat (SSR) markers determined localization of the T. timopheevii genome in chromosomes 1A, 2A, 2B, 5A, 5B, and 6B. A population of F2 offspring of crossing hybrid line 842-2 with common wheat cultivar Skala was obtained for mapping the loci controlling leaf rust resistance. Analysis of association of phenotypic and genotypic data by means of simple interval mapping (SIM) and composite interval mapping (CIM) has shown that the resistance of adult plants is determined by two loci in chromosomes 5B and 2A. The major locus QLr.icg-5B, transferred from T. timopheevii chromosome 5G mapped to the interval of microsatellite loci Xgwm408-Xgwm1257 controls 72% of the phenotypic variance of the trait. The other, minor locus QLr.icg-2A located to chromosome 2A at a distance of 10 cM from Xgwm312 accounts for 7% of the trait expression. Microsatellite markers located near these loci may be used for controlling the transfer of agronomically valuable loci when new lines and cultivars are created. [ABSTRACT FROM AUTHOR]

The quantitative trait loci (QTL) associated with individual characteristics of grain and flour quality in wheat lines grown under contrasting environmental conditions were mapped. Overall, 22 QTL that manifested under contrasting environmental conditions with various significances were detected on 10 chromosomes. Grain hardness and vitreousness were associated with three loci on chromosomes 5D, 6A, and 3A, while the gluten content, with two loci on chromosomes 5B and 7A. Dough extensibility was associated with only one QTL localized in the region of Glu-A1 locus. One of the loci determining flour and dough strengths is located in the region of Gli-B1 and Glu-B3 loci and the rest, in various regions of chromosomes 1B, 5D, and 4B, where no particular genes associated with grain quality have been yet found. The detected QTL can be used in further experiments on genetic control of gluten formation and quality in wheat. [ABSTRACT FROM AUTHOR]

Two major genes controlling leaf pubescence were mapped on chromosomes 4BL ( Hl1) and 7BS ( Hl2 Aesp ) in wheat (Saratovskaya 29) and a wheat/ Aegilops introgression line (102/00I), respectively, together with quantitative trait loci (QTLs) determining hairiness of the leaf margin ( QHl.ipk-4B, QHl.ipk-4D) and auricle ( QPa.ipk-4B, QPa.ipk-4D) on the long arms of chromosomes 4B and 4D, respectively. The QTLs on chromosome 4D were contributed by a synthetic wheat and, therefore, originated from Aegilops tauschii. The homoeologous group 4 wheat/ A. tauschii genes/QTLs detected in the present study were aligned with the barley pubescence genes Hln/ Hsh and Hs b and the hairy peduncle rye gene Hp1. The locus seems to be pleiotropically responsible for the pubescence of different plant organs in different species of the Triticeae. Another homoeologous series may be present on the short arms of the homoeologous group 7 chromosomes, based on the results of an allelic test cross between the Chinese local cultivar Hong-mang-mai carrying Hl2 and the wheat/ Aegilops speltoides introgression line 102/00I. [ABSTRACT FROM AUTHOR]

Complementary genes for purple grain colour Pp1, Pp2, Pp3 (now designated Pp1, Pp3b, Pp3a, respectively) were mapped using crosses between purple-grained hexaploid wheats 'Purple Feed' – Pp1Pp1/Pp2Pp2 ( Pp1Pp1/Pp3bPp3b), 'Purple' – Pp1Pp1/Pp3Pp3 ( Pp1Pp1/Pp3aPp3a) with non-purple-grained cultivars 'Novosibirskaya 67' ('N67') and 'Saratovskaya 29' ('S29'). The genes Pp2 ( Pp3b) and Pp3 (Pp3a) were inherited as monofactorial dominant when purple-grained wheats were crossed to 'N67'. Both were mapped in the centromeric region of the chromosome 2A. Therefore, they were suggested being different alleles at the same locus and designated Pp3a and Pp3b. In the crosses between purple-grained wheats and 'S29' a segregation ratio of 9 (purple) to 7 (non purple) was obtained suggesting a complementary interaction of two dominant genes, Pp1 and Pp3. To map Pp1 as a single gene, the influence of the other Pp gene was taken into consideration by determining the Pp3 genotype of the F2 plants. The gene was mapped on chromosome 7BL, about 24 cM distal to the centromere. The Pp1gene was shown to be non allelic to the Rc-1 (red coleoptile) and Pc (purple culm) genes, contrary to what was previously suggested. The colouration caused by the Pp genes has no effect on pre-harvest sprouting. [ABSTRACT FROM AUTHOR]

Copyright of Genome is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Genome is the property of Canadian Science Publishing and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Greenbug and Russian wheat aphid (RWA) are two devastating pests of wheat. The first has a long history of new biotype emergence and. recently. RWA resistance has just started to break down. Thus, it is necessary to find new sources of resistance that will broaden the genetic base against these pests in wheat. Seventy-five doubled haploid recombinant (DHR) lines for chromosome 6A from the F1 of the cross between "Chinese Spring' and the "Chinese Spring (Synthetic 6A) (Triticum dicoccoide.s x Aegilops tauschii)' substitution line were used as a mapping population for testing resistance to greenbug biotype C and lo a new strain of RWA that appeared in Argentina in 2003. A quantitative trait locus (QTL) for antixenosis to greenbug was significantly associated with the marker loci Xgwm1009 and Xgwm1185 located in the centromere region of chromosome 6A. Another QTL which accounted for most of the antixenosis against RWA was associated with the marker loci Xgwm1293 and Xgwm1150, both located on the long arm of chromosome 6A. This is the first report of greenbug and RWA resistance genes located on chromosome 6A. It is also the first report of antixenosis against the new strain of RWA. As most of the RWA resistance genes present in released cultivars have been located in [he D-genome, it is highly desirable to find new sources in other genomes to combine the existing resistance genes with new sources. [ABSTRACT FROM AUTHOR]

The objective of this study was to assess genetic diversity within old and modern common spring wheat ( Triticum aestivum L.) varieties cultivated in Siberia and to find out whether old Siberian varieties could be a potential source for genetic diversity in modern wheat breeding in Siberia. A set of 54 varieties was analysed using 22 wheat microsatellite markers (WMS), determining 23 loci located on 19 different chromosomes. In total, 151 alleles were detected with an average of 6.6, ranging from three to 11 alleles per locus. The average genetic diversity value (polymorphic information content) was 0.70. WMS located in the B genome produced more alleles per locus (7.6) compared with WMS located in the A (6.0) and D (6.0) genomes. Genetic similarity values between varieties ranged from 0.19 to 0.96 and were used to produce a dendrogram. With a few exceptions the varieties studied were clustered in two nearly equal groups consisting of predominantly old (released before 1960) and modern (released in 1960–90s) varieties, respectively. Genetic diversity values within these two groups were similar with 0.60 and 0.58, respectively. The numbers of group-specific alleles were 34 and 29, respectively. A significant variation in frequencies of 79 shared alleles was observed. The results obtained by using genomic microsatellite sequences demonstrated that breeding has not resulted in a decrease in the genetic diversity in Siberian spring wheat. However, significant quantitative and qualitative changes in allelic frequencies of different loci were detected. It may be suggested, that old Siberian common spring wheat varieties are a potential basis for genetic diversity in modern wheat breeding in Siberia. [ABSTRACT FROM AUTHOR]

An F[SUB2] population segregating for the dominant gene Vrn-B1 was developed from the cross of the substitution line 'Diamant'/'Miro-novskaya 808 5A' and the winter wheat cultivar 'Bezostaya 1'. Microsatellite markers (Xgwm and Xbarc) with known map locations on chromosome 5B of common wheat were used for mapping the gene Vrn-B1. Polymorphism between parental varieties was observed for 28 out of 34 microsatellite markers (82%). Applying the quantitative trait loci mapping approach, the target gene was mapped on the long arm of chromosome 5B, closely linked to Xgwm408. The map position of Vrn-B1 suggests that the gene is homoeologous to other vernalization response genes located on the homoeologous group 5 chromosomes of wheat, rye and barley. [ABSTRACT FROM AUTHOR]

The aim of this study was to evaluate the suitability of sequence tagged microsatellite site (STMS) markers for varietal identification and discrimination in tomato. For this purpose, a set of 20 STMS primer pairs was used to construct a database containing the molecular description of the most common varieties (>500) of tomato grown in Europe. The database was built and tested by a consortium of five European laboratories each using a different STMS detection system. In this way, it could be demonstrated that the STMS markers and database were suitable for use in network activities where a common database is being established on a continuing basis with data from different laboratories. Microsatellite polymorphism in tomato was found to be relatively low. The number of alleles per locus ranged from 2 to 8 with an average of 4.7 alleles per locus. Nevertheless, more than 90% of the varieties had different microsatellite profiles. A "blind testing" exercise showed that in general, identification of unknown samples (or detecting the most similar variety) with the 20 markers and the database was relatively easy for homogeneous varieties but less certain with heterogeneous varieties when using pools of 6 individuals. [ABSTRACT FROM AUTHOR]

In hexaploid bread wheat (Triticum aestivum L. em. Thell), ten members of the IWMMN (International Wheat Microsatellites Mapping Network) collaborated in extending the microsatellite (SSR = simple sequence repeat) genetic map. Among a much larger number of microsatellite primer pairs developed as a part of the WMC (Wheat Microsatellite Consortium), 58 out of 176 primer pairs tested were found to be polymorphic between the parents of the ITMI (International Triticeae Mapping Initiative) mapping population W7984 × Opata 85 (ITMIpop). This population was used earlier for the construction of RFLP (Restriction Fragment Length Polymorphism) maps in bread wheat (ITMImap). Using the ITMIpop and a framework map (having 266 anchor markers) prepared for this purpose, a total of 66 microsatellite loci were mapped, which were distributed on 20 of the 21 chromosomes (no marker on chromosome 6D). These 66 mapped microsatellite (SSR) loci add to the existing 384 microsatellite loci earlier mapped in bread wheat. [ABSTRACT FROM AUTHOR]

For intrachromosomal mapping of the dominant GA-sensitive dwarfing gene Rht12 and the vernalization response gene VrnI on chromosome 5 A, an F2 population was established using a wide (synthetic) wheat cross. In addition to restriction fragment length polymorphism (RFLP) probes four microsatellite markers were incorporated. Rht12 was mapped distally to four RFLP loci (Xmwg616, Xpsr164, Xwg114, Xpsr1201) and three microsatellite markers (Xgwm179, Xgwm410, Xgwm291), known to be located on the segment of chromosome 5AL which was ancestrally translocated and is homoeologous to Triticeae 4L. The map position of Rht12 suggests that it is homoeologous to the dominant GA-sensitive dwarfing gene Ddwl, present on chromosome 5RL. The vernalization response gene Vrnl showed linkage to Xwg644, as might be expected from comparative maps. [ABSTRACT FROM AUTHOR]