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1.
Summary Wild relatives of common wheat, Triticum aestivum, and related species are an important source of disease and pest resistance and several useful traits have been transferred from these species to wheat. C-banding and in situ hybridization analyses are powerful cytological techniques allowing the detection of alien chromatin in wheat. C-banding permits identification of the wheat and alien chromosomes involved in wheat-alien translocations, whereas genomic in situ hybridization analysis allows determination of their size and breakpoint positions. The present review summarizes the available data on wheat-alien transfers conferring resistance to diseases and pests. Ten of the 57 spontaneous and induced wheat-alien translocations were identified as whole arm translocations with the breakpoints within the centromeric regions. The majority of transfers (45) were identified as terminal translocations with distal alien segments translocated to wheat chromosome arms. Only two intercalary wheat-alien transloctions were identified, one induced by radiation treatment with a small segment of rye chromosome 6RL (H25) inserted into the long arm of wheat chromosome 4A, and the other probably induced by homoeologous recombination with a segment derived from the long arm of a group 7 Agropyron elongatum chromosome with Lr19 inserted into the long arm of 7D. The presented information should be useful for further directed chromosome engineering aimed at producing superior germplasm.Contribution No. 96-55-J from the Kansas Experimental Station, Kansas State University, Manhattan, KS 66506-5502, USA.  相似文献   

2.
N. Jouve  F. Diaz 《Euphytica》1990,47(2):165-169
Summary The EST-6 leaf esterase phenotypes from euploid, nullisomic-tetrasomic and rye chromosome addition and substitution lines of common wheat were determined using polyacrylamide gel electrophoresis. Evidence is presented to demonstrate that Est-6 is a new set of genes, that are expressed in the leaf. The Est-6 gene set were clearly distinguished from the Est-5 genes which are expressed in the grain. The three homoeoallelic loci, Est-A6, Est-B6 and Est-D6, were located on chromosomes 3A, 3B and 3D. An Est-R6 gene was located on chromosome 6R is involved in rye. Some considerations concerning homoeology between homoeologous group 3 of wheat and the rye chromosome 6R are made.  相似文献   

3.
End-use quality of wheat for noodles is influenced by polyphenol oxidase activity and its corresponding substrates. This study investigated the chromosomal location of genes that determine phenol colour reaction of kernels in tetraploid wheat using aneuploid stocks. Polyphenol oxidase activity was estimated by the colour reaction of kernels to phenol solution. It was found that the genes located on homoeologous group 2 chromosomes have an important effect on the level of phenol colour reaction of kernels. The genes (Tc1 and Tc2) responsible for high phenol colour reaction of kernels were mapped to the long arms of chromosome 2A and chromosome 2B, respectively. The map distances were estimated to be 46.8 cM for Tc1 and 40.7 cM for Tc2 from the centromere using double-diltelosomics of durum wheat.  相似文献   

4.
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.  相似文献   

5.
Summary Alien dominant genes of spring habit were introgressed into bread wheat. The introgression was undertaken by simple crossing of winter bread wheat to related spring species or genera, followed by backcrossing to winter bread wheat, and did not involve the use of the ph mutants or embryo culture. The introgressed genes were located mostly on chromosomes of homoeologous group 5, and were allelic to the known Vrn genes in bread wheat. Nevertheless three groups of lines were discovered with the genes possibly located on other chromosomes. These genes were non-allelic to each other and to known Vrn genes and were designated Vrn6 Sc , Vrn7 Sc (introgressed from Secale cereale) and Vrn8 Ts (from Triticum sphaerococcum).  相似文献   

6.
Previous studies in several Triticeae species have suggested that salt tolerance is a polygenic trait, but that genes on some chromosomes confer better tolerance to salt stress than others. This suggests an intriguing possibility that there may be a similar basis for salt tolerance in the species of the tribe Triticeae. In this study, chromosomal control of the tolerance to sudden salt stress, measured as the mean rate of leaf elongation in solution cultures with a single increment of 200 mM NaCl, was investigated in the genomes of cultivated barley (Hordeum vulgare L.), rye (Secale cereale L.), and Dasypyrum villosum (L.) Can-dargy by using disomic addition lines of individual pairs of chromosomes or chromosome arms of each of the three species in the ‘Chinese Spring’ wheat genetic background. It was observed that the chromosomes of homoeologous groups 3, 4, and 5 in barley, 5 and 7 in rye, and 4 and 6 in D. villosum carry loci with significant positive effects on salt tolerance. Increased doses of chromosomes of group 2, however, reduce or do not increase the tolerance to salt stress. These results are in agreement with a previous study of the tolerance of this salt stress regime in wheat and wheatgrass Lophopyrum elongatum. A ranking analysis of the chromosomal effects within each genome of the five Triticeae species investigated in this and previous studies revealed that the chromosomes of homoeologous groups 3 and 5 consistently confer large positive effects on the tolerance of sudden salt stress, while the chromosomes of homoeologous group 2 in increased dose have no or negative effects on the tolerance. This strongly suggests that species of the tribe Triticeae share some common genetic mechanisms of tolerance of sudden salt stress. The findings in this study give credence to the proposal that wild relatives can be exploited in the development of wheat cultivars with greater tolerance to salt stress.  相似文献   

7.
Leaf and stripe rusts are severe foliar diseases of bread wheat. Recently, chromosomes 5Mg from the related species Aegilops geniculata that confers resistance to both leaf and stripe rust and 5Ut from Ae. triuncialis conferring resistance to leaf rust have been transferred to bread wheat in the form of disomic DS5Mg(5D) and DS5Ut(5A) chromosome substitution lines. The objective of this study was to shorten the alien segments in these lines using Ph I-mediated, induced homoeologous recombination. Putativerecombinants were evaluated for their rust resistance, and by genomic in situ hybridization and microsatellite analyses. One agronomically useful wheat-Ae. geniculata recombinant resistant to leaf and stripe rust was identified that had only a small terminal segment of the 5MgL arm transferred to the long arm of an unidentified wheat chromosome. This germplasm can be used directly in breeding programs. Only one leaf rust-resistant wheat-Ae. triuncialis recombinant, which consists of most of the complete 5Ut chromosome with a small terminal segment derived from 5AS, was identified. This germplasm will need further chromosome engineering before it can be used in wheat improvement. This revised version was published online in August 2006 with corrections to the Cover Date.  相似文献   

8.
I. Leonova    E. Pestsova    E. Salina    T. Efremova    M. Röder  A. Börner  G. Fischbeck 《Plant Breeding》2003,122(3):209-212
An F2 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.  相似文献   

9.
Waiting for fine times: genetics of flowering time in wheat   总被引：17，自引：0，他引：17  
To maximise yield potential in any environment, wheat cultivars musthave an appropriate flowering time and life cycle duration which`fine-tunes' the life cycle to the target environment. This in turn, requiresa detailed knowledge of the genetical control of the key components of thelife cycle. This paper discusses our current knowledge of the geneticalcontrol of the three key groups of genes controlling life-cycle duration inwheat, namely those controlling vernalization response, photoperiodresponse and developmental rate (`earliness per se', Eps genes).It also discusses how our ability to carry out comparative mapping of thesegenes across Triticeae species, and particularly with barley, is indicatingnew target genes for discovery in wheat. Major genes controllingvernalization response, the Vrn-1 series, have now been located bothgenetically and physically on the long arms of the homoeologous group fivechromosomes. These genes are homoeologous to each other and to thevernalization genes on chromosomes 5H of barley and 5R of rye.Comparative analysis with barley also indicates that other series ofvernalization response genes may exit on chromosomes of homoeologousgroups 4 (4B, 4D, 5A) and 1. The major genes controlling photoperiodresponse in wheat, the Ppd-1 genes, are located on the homoeologousgroup 2 chromosomes, and are homoeologous to a gene on barleychromosome 2H. Mapping in barley also indicates a photoperiod responselocus on barley 1H and 6H, indicating that a homoeologous series shouldexist on wheat group 1 and 6 chromosomes. In wheat, only a few`earliness per se loci have been located, such as on chromosomes ofhomoeologous group 2. However, in barley, all chromosomes appear tocarry such loci, indicating that several series of loci that affectdevelopmental rate independent of environment remain to be discovered.Overall, comparative studies indicate that there are probably twenty-fiveloci controlling the duration of the life-cycle, Vrn, Ppd and Eps genes, that remain to be mapped in wheat. There are major gaps inour knowledge of the detailed physiological effects of genes discovered todate on the timing of the life cycle from different sowing dates. This isbeing addressed by studying the phenology of isogenic and deletion lines inboth field and controlled environmental conditions. This has indicated thatthe vernalization genes have major effects on the rate of primodiaproduction, whilst the photoperiod genes affect the timing of terminalspikelet production and stem elongation, and these effects interact withsowing date.  相似文献   

10.
Previously chromosome 3A of wheat (Triticum aestivum L.) was reported to carry genes influencing yield, yield components, plant height, and anthesis date. The objective of current study was to survey various molecular marker systems for their ability to detect polymorphism between wheat cultivars Cheyenne(CNN) and Wichita (WI), particularly for chromosome3A. Seventy-seven `sequence tagged site' (STS), 10simple sequence repeat (SSR), 40 randomly amplified polymorphic DNA (RAPD) markers, and 52 restriction fragment length polymorphism (RFLP) probes for wheat homoeologous group 3 chromosomes, were investigated. Three (3.9%) STS-PCR primer sets amplified polymorphic fragments for the two cultivars, of which one was polymorphic for chromosome 3A. Sixty percent of SSR markers detected polymorphism between CNN and WI of which 50% were polymorphic for chromosome 3A. Twenty percent of RAPD markers detected polymorphism between CNN and WI in general, but none of these detected polymorphism for chromosome 3A. Of the fifty-two RFLP probes, 78.8% detected polymorphism between CNN and WI for group 3 chromosomes with one or more of seven restriction enzymes and 42% of the polymorphic fragements were for chromosome 3A. These high levels of RFLP and SSR polymorphisms between two related wheat cultivars could be used to map and tag genes influencing important agronomic traits. It may also be important to reconsider RFLP as the most suitable marker system at least for anchor maps of closely related wheat cultivars. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   

11.
Y. Li  Y. Song  R. Zhou  G. Branlard  J. Jia 《Plant Breeding》2009,128(3):235-243
Whereas gluten fraction accounts for 30–60% of the variation in wheat bread‐making quality, there remains substantial variation determined by non‐gluten factors. The objective of this study was to detect new loci for wheat quality. The genetics of sodium dodecyl sulphate‐sedimentation volume (Ssd), grain hardness (GH), grain protein content, wet gluten content (WGC) and water absorption (Abs) in a set of 198 recombinant inbred lines derived from two commercial varieties was studied by quantitative trait loci (QTL) analysis. A genetic map based on 255 marker loci, consisting of 250 simple sequence repeat markers and five glutenin loci, Glu‐A1, Glu‐B1, Glu‐D1, Glu‐B3 and Glu‐D3, was constructed. A total of 73 QTLs were detected for all traits. A major QTL for GH was detected on chromosome 1B and its relative contribution to phenotypic variation was 27.7%. A major QTL for Abs on chromosome 5D explained more than 30% of the phenotypic variation. Variations in Ssd were explained by four kinds of genes. Some QTLs for correlated traits mapped to the same regions forming QTL clusters or indicated pleiotropic effects.  相似文献   

12.
To complement previously developed recombinant chromosomes 1R.1D, two series of translocations involving the Glu-D1 gene from chromosome ID to chromosome 1A were produced in hexaploid triticale. These series involve seven independent transfers of allele d encoding for high molecular weight glutenin subunits 5+10 and ten independent transfers involving allele a encoding for HMW glutenin subunits 2 + 12. The frequency of homoeologous recombination between chromosomes 1A and 1D was within the range observed for pairs of homologues in wheat, supporting earlier observations that homoeologous recombination in triticale is frequent. Recombined chromosomes 1A.1D can be used to introduce the Glu-D1 gene to durum wheats, and to manipulate the dosage of Glu-D1 in hexaploid triticale and bread wheat.  相似文献   

13.
B. Keller  N. Stein  C. Feuillet 《Euphytica》2001,119(1-2):131-133
The hexaploid wheat genome is too complex for direct map-basedcloning and model genomes have to be used to isolate genes from wheat.Comparative genomic analysis at the genetic map level has shown extensiveconservation of the gene order between the different grass genomes inmany chromosomal regions. However, little is known about the geneorganization in grass genomes at the microlevel. We have investigated themicrocollinearity at Lrk gene loci in the genomes of four grass species:wheat, barley, maize and rice. The Lrk genes, which encodereceptor-like kinases, were found to be consistently associated with anothertype of receptor-like kinase (Tak) on chromosome groups 1 and 3 inTriticeae and on chromosomes homoeologous to Triticeae group 3 in theother grass genomes. On Triticeae chromosome group 1, Tak and Lrk together with genes putatively encoding NBS/LRR proteins form acluster of genes. Comparison of the gene composition at orthologous Lrk loci in wheat, barley and rice revealed a maximal gene density of onegene per 5 kb. We conclude that small and large grass genomes containregions which are highly enriched in genes. Microrearrangements betweendifferent grass genomes have been found and therefore, the choice of agood model genome is critical. We have recently started to work on theT. monococcum model genome and confirmed its usefulness foranalysis of the Lr10 leaf rust disease resistance locus in wheat.  相似文献   

14.
V. Korzun    M. Röder    A. J. Worland  A. Börner 《Plant Breeding》1997,116(3):227-232
For intrachromosomal mapping of the dominant GA-sensitive dwarfing gene Rht12 and the vernalization response gene Vrn1 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 SAL which was ancestrally translocated and is homoeologous to Triticeae 4 L. The map position of Rht12 suggests that it is homoeologous to the dominant GA-sensitive dwarfing gene Ddw1, present on chromosome 5RL. The vernalization response gene Vrn1 showed linkage to Xwg644, as might be expected from comparative maps.  相似文献   

15.
Liguleless phenotypes of wheat lack ligule and auricle structures on all leaves of the plant. Two recessive genes principally control the liguleless character in tetraploid wheat. The F2 progenies of k17769 (liguleless mutant)/Triticum dicoccoides and k17769/T. dicoccum segregated in a 15:1 ratio, whereas the F2 progenies of k17769/T. durum and k17769/T. turgidum segregated in a 3:1 ratio. A new gene, lg3, was found on chromosome 2A. Segregation of F2 progenies between k17769 and chromosome substitution lines for homoeologous group 2 chromosomes suggested that the liguleless genotype had occurred by mutation at the lg3 locus on chromosome 2A, and then by mutation at the lg1 locus on chromosome 2B, in the process of domestication of tetraploid wheat. The gene (lg1) was linked to Tc2 (11.9 cM), which determines phenol colour reaction of kernels, on the long arm of chromosome 2B. The distance of lg1 to the centromere was found to be 60.4 cM, and microsatellite mapping established the gene order, centromere – Xgwm382 – Xgwm619 – Tc2 – lg1 on the long arm of chromosome 2B.  相似文献   

16.
The introgression of desirable genes or alleles from the wild relatives of hexaploid wheat can be a valuable source of genetic variation for wheat breeders to enhance modern varieties. The UK Group 1 bread making variety Shamrock is an example where the introgression of genetic material from wild emmer (Triticum dicoccoides) has been used to develop a modern cultivar. A striking character of Shamrock is its unique viridescent colour compared to other UK wheats, a trait that coincides with a non-glaucous phenotype. A doubled haploid population segregating for the trait (Shamrock × Shango) was examined to map the location of Vir, and analyse any associated pleiotropic effects. The viridescence gene located to the distal end of the short arm of chromosome 2B. QTL analysis of productivity traits shows an association between Vir and a significant delay in senescence, resulting in an extension of the grain filling period. A stable yield QTL, accounting for up to a quarter of the variation in one case, was also identified at or near Vir, indicating significant yield benefits either by linkage or pleiotropy.  相似文献   

17.
Stagonospora nodorum blotch (SNB) is an important foliar disease of durum wheat (Triticum turgidum var. durum) worldwide. The combined effects of SNB and tan spot, considered as components of the leaf spotting disease complex, result in significant damage to wheat production in the northern Great Plains of North America. The main objective of this study was the genetic analysis of resistance to SNB caused by Phaeosphaeria nodorum in tetraploid wheat, and its association with tan spot caused by Pyrenophora tritici-repentis race 2. The 133 recombinant inbred chromosome lines (RICL) developed from the cross LDN/LDN(Dic-5B) were evaluated for SNB reaction at the seedling stage under greenhouse conditions. Molecular markers were used to map a quantitative trait locus (QTL) on chromosome 5B, explaining 37.6% of the phenotypic variation in SNB reaction. The location of the QTL was 8.8 cM distal to the tsn1 locus coding for resistance to P. tritici-repentis race 2. The presence of genes for resistance to both SNB and tan spot in close proximity in tetraploid wheat and the identification of molecular markers linked to these genes or QTLs will be useful for incorporating resistance to these diseases in wheat breeding programs.  相似文献   

18.
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 2Am, respectively. On the other hand, C and Zeo, on chromosome 2H, did not appear to be orthologous.  相似文献   

19.
Structural genes for leaf dimeric phosphatases (E.C. 3.1,3.2.) have been located on wheat chromosome arms 7BL and 7DL. No gene was found on 7AL. The results obtained pointed to the existence of two kinds of wheat phosphatases (monomers and dimers j located on different homoeologous groups, which is in agreement with results found in Secale cereale and Agropyron intermedium. These results allow homoeologous relationships to be established through the classification of dimeric phosphatases and also provides another useful genetic marker for the 7BL and 7DL arms., They also provide further support for die concept of the conservation of gene synteny groups within the Triticnae.  相似文献   

20.
The differences between effects of homoeologous group 5 chromosomes on growth phases and agronomic characters were studied by using reciprocal substitution lines between a winter wheat cultivar with a high vernalization requirement (Mironovskaya 808) and one with lowvernalization requirement (Bezostaya 1), in which the presence of different recessive vrn alleles is supposed. The two cultivars and the substitution lines Mironovskaya 808 (Bezostaya 1 5A), Mironovskaya 808 (Bezostaya 1 5B), Mironovskaya 808 (Bezostaya 1 5D), Bezostaya1 (Mironovskaya 808 5A), Bezostaya 1 (Mironovskaya 808 5B),Bezostaya 1 (Mironovskaya 808 5D) were grown at 10 different sowing dates. The results showed that differences between the homoeologous group 5 chromosomes of Mironovskaya 808 and those of Bezostaya 1influenced the growth phases in addition to the impact by the genetic background and sowing date. We inferred from the analysis and comparison of their effect on vernalization response that vrn loci on these chromosomes influence growth phases. It is probably due to pleiotropic effects of the loci. The rare occurrence of significant interactions between group 5 chromosomes × sowing dates probably indicates independence of their effect. Agronomic characters were also markedly influenced by sowing date and the difference in backgrounds between Mironovskaya 808 and Bezostaya 1. A significant impact by at least two of the chromosomes on almost all studied characters was detected. The chromosomes affected the combined characters in the order5D>5B>5A and the positive value of the differences suggests that a content of Mironovskaya 808 chromosomes is more advantageous. It was possible to find certain indices in some agronomic traits, supporting the idea that the expression of some characters can also be connected to vernalization requirement and thus to the expression of the vrn loci. This supposition is most probable in the number of tillers and number of spikes. In some traits significant interactions occurred between homoeologous group 5 chromosomes × genetic background. Sporadic and low significance between homoeologous group 5 chromosomes × sowing dates suggest that the genetic effect of these chromosomes is independent of environmental conditions. This revised version was published online in July 2006 with corrections to the Cover Date.  相似文献   

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