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1.
Liu Shubing  Wang Honggang 《Euphytica》2005,143(1-2):229-233
Among the progenies of a hybrid between common wheat Triticum aestivum L. cv. Yannong 15 and Thinopyron intermedium, plant E99018 was identified with the chromosome number 2n = 42 and stable agronomic traits. An analysis of the metaphase chromosome pairing indicated that it formed 21 bivalents but that 2 univalents were present in the F1 hybrid of this plant with common wheat. Resistance verification by race 15 and with mixed races of Blumeria graminis f. sp. tritici at the seedling and adult stages showed that at both stages, the plant was immune to powdery mildew. In situ hybridization with the genomic Th. intermedium and the St genome DNAs as probes and wheat DNA as a block has shown that it contained a pair of Th. intermedium chromosomes. On the basis of the hybridization pattern of the St genome probe to the critical chromosome, a conclusion was reached that this pair of chromosomes belonged to the E genome. Therefore, plant E99018 was a spontaneously formed substitution line. An analysis by 116 SSR markers indicated that the substituted wheat chromosome was 2D and the most likely substitution in E99018 is 2E(2D).  相似文献   

2.
We developed some wheat-Th. intermedium translocation lines,Yw642, Yw443 and Yw243, etc., showing good BYDV resistance from L1by induced homoeologous pairing using CS ph mutant. Characterization ofthese wheat lines was carried out by GISH and RFLP analysis. The resultsof GISH showed that the lines, YWw42, Yw443 and Yw243, etc., arehomozygous wheat-Th. intermedium translocation lines, in which thechromosome segments of Th. intermedium were transferred to thedistal end of a pair of wheat chromosomes. RFLP analysis indicated that thetranslocation chromosome of the wheat lines is T7DS · 7DL-7XL. Thebreakpoint of the translocation is located on the distal end of 7DL, betweenXpsr965 and Xpsr680 about 90–99 cm from the centromere. The BYDVgene is located on the distal end of 7XL around Xpsr680, Xpsr687 andXwg380. The RFLP markers of psr680, psr687 and wg380 werecosegregated with the BYDV resistance respectively and could be used formolecular assisted selection (MAS) in wheat breeding program for BYDVresistance.  相似文献   

3.
G. F. Marais 《Plant Breeding》1990,104(2):152-159
A Thinopyrum distichum chromosome segment translocated on chromosome arm 7DL. of the line ‘Indis’, was shown to be preferentially transmitted in crosses with other bread wheats. The translocated segment carries a gene for leaf rust resistance and produces a null condition for the endopeptidase product, EP-Dla. These characters were used to follow the transmission of the translocated chromosome in segregating and testcross progenies derived by crossing ‘Indis’ to four bread wheat cultivars. The severity of the gametocidal response in the heterozygotes ranged from a virtually exclusive transfer of the translocation to an almost normal transmission of the homologues. In some genetic backgrounds an intermediate level of transmission occurred. In the F1 with a gametocidal response, the transmission of the normal chromosome 7D was reduced in both sexes, but the reduction may be more severe in the male germline.  相似文献   

4.
Chromosome compositions of seven lines, derived from hybrids between a wheat cultivar and the wheat-Thinopyrum intermedium addition line Z6, with barley yellow dwarf virus (BYDV) resistance, were determined by genomic in situ hybridization, cytogenetic and SSR assays. The results showed that line N522 was a disomic addition line, lines N420 and N439 were 2Ai-2(2B) chromosome substitution lines, lines N431 and N452 were 2Ai-2(2D) chromosome substitution lines, line N523 was a 2Ai-2S(2D) ditelosomic substitution line, and line N530 was a double ditelosomic line with the mitotic chromosome number of 2n = 40 + 4t. One pair of telosomes in line N530 lacked several proximal SSR markers of chromosome 2AS, but possessed certain terminal markers, which were consistent with an acrocentric structure, and the other pair of chromosome arms were presumably 2Ai-2S telosomes with BYDV-resistance. These wheat-Th. intermedium lines provide useful genetic resources for developing alien chromosome translocation lines.  相似文献   

5.
Z. S. Lin    D. H. Huang    L. P. Du    X. G. Ye    Z. Y. Xin 《Plant Breeding》2006,125(2):114-119
Among the regenerated plants derived from immature hybrid embryos of wheat–Thinopyrum intermedium disomic addition line Z6 × common wheat variety ‘Zhong8601’, a plant with a telocentric chromosome and barley yellow dwarf virus (BYDV) resistance was obtained. The telocentric chromosome paired with an entire Thinopyrum chromosome to form a heteromorphic bivalent at meiotic metaphase I. Genomic in situ hybridization showed that the telosome originated from Th. intermedium. Two ditelosomic additions and one disomic substitution were identified among the offspring of the plant. Two random amplified polymorphic DNA molecular markers were identified among 150 random primers used to detect the different arms of the alien chromosome. These might be useful for developing translocation lines with BYDV resistance.  相似文献   

6.
Powdery mildew caused by Blumeria graminis (DC) Speer f. sp. tritici Em. Marchal is a serious disease of wheat (Triticum aestivum L.) in Southwestern China. A line of common wheat designated 08-723 isolated from the progeny of a hybrid between common wheat and Thinopyrum intermedium (Host) Barkworth & Dewey, was highly resistant to the existing powdery mildew races in the region. This line had a similar phenotype to its wheat parent, and it showed normal bivalent pairing at metaphase I of meiosis. It was analyzed by genomic in situ hybridization, fluorescence in situ hybridization and sequential C-banding-GISH to determine the amount, location and origin of the alien chromatin present. The results revealed that line 08-723 is homozygous for a two-point translocation replacing chromosome 6A of wheat. The translocation chromosome appears to have a normal 6AL arm; its short arm has a short terminal segment of ca. 10 % in length originating from an unidentified B-genome chromosome of wheat and a long proximal segment of ca. 90 % of the arms’ length originating from one of the St-genome chromosomes of Th. intermedium. Genetic analysis of powdery mildew resistance in F1, F2 and F2:3 populations from a cross of 08-723 with a susceptible wheat line indicated that the resistance was controlled by a single dominant gene and in a sample of F2 plants it always associated with the translocated chromosome. The gene responsible for resistance on the translocated chromosome may provide an alternate source of resistance in wheat breeding programs.  相似文献   

7.
Leaf rust caused by the fungus Puccinia triticina is one of the most important diseases of wheat (Triticum aestivum) worldwide. The use of resistant wheat cultivars is considered the most economical and environment-friendly approach in controlling the disease. The Lr38 gene, introgressed from Agropyron intermedium, confers a stable seedling and adult plant resistance against multiple isolates tested in Europe. In the present study, 94 F2 plants resulting from a cross made between the resistant Thatcher-derived near-isogenic line (NIL) RL6097, and the susceptible Ethiopian wheat cultivar Kubsa were used to map the Thatcher Lr38 locus in wheat using simple sequence repeat (SSR) markers. Out of 54 markers tested, 15 SSRs were polymorphic between the two parents and subsequently genotyped in the population. The P. triticina isolate DZ7-24 (race FGJTJ), discriminating Lr38 resistant and susceptible plants, was used to inoculate seedlings of the two parents and the segregating population. The SSR markers Xwmc773 and Xbarc273 flanked the Lr38 locus at a distance of 6.1 and 7.9 cM, respectively, to the proximal end of wheat chromosome arm 6DL. The SSR markers Xcfd5 and Xcfd60 both flanked the locus at a distance of 22.1 cM to the distal end of 6DL. In future, these SSR markers can be used by wheat breeders and pathologists for marker assisted selection (MAS) of Lr38-mediated leaf rust resistance in wheat.  相似文献   

8.
Stripe (yellow) rust, caused by Puccinia striiformis f. sp. tritici (Pst), is one of the most devastating wheat diseases worldwide. Triticum aestivum-Haynaldia villosa 6VS/6AL translocation lines carrying the Yr26 gene on chromosome 1B, are resistant to most races of Pst used in virulence tests. In order to better utilize Yr26 for wheat improvement, we attempted to screen SSR and EST-based STS markers closely linked with Yr26. A total of 500 F2 plants and the F2:3 progenies derived from a cross between 92R137 and susceptible cultivar Yangmai 5 were inoculated with race CYR32. The analysis confirmed that stripe rust resistance was controlled by a single dominant gene, Yr26. Among 35 pairs of genomic SSR markers and 81 pairs of STS markers derived from EST sequences located on chromosome 1B, Yr26 was flanked by 5 SSR and 7 STS markers. The markers were mapped in deletion bins using CS aneuploid and deletion lines. The closest flanking marker loci, Xwe173 and Xbarc181, mapped in 1BL and the genetic distances from Yr26 were 1.4 cM and 6.7 cM, respectively. Some of these markers were previously reported on 1BS. Eight common wheat cultivars and lines developed from the T. aestivum-H. villosa 6VS/6AL translocation lines by different research groups were tested for presence of the markers. Five lines with Yr26 carried the flanking markers whereas three lines without Yr26 did not. The results indicated that the flanking markers should be useful in marker-assisted selection for incorporating Yr26 into wheat cultivars.  相似文献   

9.
I. A. Khan 《Plant Breeding》2000,119(1):25-29
Thirty‐six wheat‐Agropyron intermedium (host) Beauv. [Syn. Trichopyrum intermedium (host) A. Love, Elytrigia intermedia (host) Nevski, Thinopyrum intermedium (host) Barkworth and Dewey] 7A/7Ai‐1 recombinant chromosomes were characterized using DNA markers. Analysis of recombinant chromosomes using 15 restriction fragment length polymorphism probes identified the homoeologous crossover products that had varying length of A. intermedium chromatin introgressed onto chromosome 7A of common wheat. The linear order of the probe loci was established along the lengths of the chromosomes. The short arm recombinants that had A. intermedium chromatin distal to the locus Xpsr108 and proximal to the locus Xpsr119 were resistant to wheat stem rust, indicating that the rust resistance gene (Sr44) was located on the distal part of chromosome arm 4Ai‐1s. The barley yellow dwarf virus (BYDV) resistance gene reported to be present on the long arm of chromosome 7Ai‐1 was found to be ineffective against the BYDV serotype used in the present study.  相似文献   

10.
Summary A Giemsa-C-banded karyotype of a partial amphiploid, Triticum turgidum L. var. durum cv. Nodak × Agropyron intermedium (Host) P.B., called MT-2, was analyzed. MT-2 is a winterhardy grasslike octoploid germplasm which survived 5 winters in Montana, and its seed weight is 3 times that of A. intermedium seed. The MT-2 C-banding karyotype shows 6 chromosome pairs each of the A and B wheat genomes with 3A and 4B missing. Chromosomes 1B and 2B are involved in a reciprocal homozygous translocation (T1BS·2BS, T1BL·2BL) which was also confirmed by a nucleolus-associated quadrivalent in an MT-2 × durum wheat backcross. In addition to the wheat chromosomes, MT-2 consistently shows 16 A. intermedium chromosome pairs which are designated from A to P. These chromosomes show C-banding patterns similar to those reported earlier in the literature. A large amount of C-banding polymorphism and structural rearrangements in A. intermedium itself presently make a definite chromosome assignment to the homeologous groups of the Triticeae difficult. The data presented are crucial for further directed manipulation of this germplasm aimed at producing valuable chromosome additions and substitutions in wheat.contribution No. J-2767 from Montana Agric. Exp. Stn.  相似文献   

11.
The leaf rust resistance gene on chromosome 7AL of ‘Chinese Spring’ transfer no. 12 derived from Thinopyrum ponticum, was transferred to durum wheat by standard backcrossing. In ‘Agatha’ and ‘Indis’ a leaf rust resistance gene from Thinopyrum ponticum and Thinopyrum ponticum respectively, is found on a translocated segment on chromosome arm 7DL. The use of the ‘Langdon’ disomic D-chromosome substitution lines for 7A and 7B resulted in the recovery of tetraploid leaf-rust resistant lines from the crosses with ‘Agatha’ in the B2F1 generation. Tetraploid lines carrying the ‘Indis’ translocation segment were recovered in the B2F2 generation. The F2 segregation ratios for rust resistance after selfing or back-crossing generally fitted a 1: 1 ratio indicating non-transmission of the translocation segments in the male gametes. Homozygous resistant plants were not obtained. Meiotic instability was observed in 28 chromosome B2 F2 derivatives of the crosses between ‘Chinese Spring’ transfer no. 12 and durum wheat.  相似文献   

12.
Taing Aung  Hugh Thomas 《Euphytica》1978,27(3):731-739
Summary The gene for mildew resistance has been succesfully transferred into the cultivated oat from the wild oat species Avena barbata by means of an irradiation-induced translocation. The translocation has been shown to involve the long arm of chromosome ST21 of A. sativa, the short arm, the centromere and a segment of the long arm of the barbata chromosome.The transmission of the translocation is normal in the cultivar Manod in which it was originally isolated. When the translocation was transferred into other cultivars of oats, transmission through the male gametes was found to be impaired in some genotypic backgrounds. However, there was no evidence that the translocation had any deleterious effect on development and fertility in a range of cultivars.The translocation was shown to involve an exchange between nonhomoeologous chromosomes.The behaviour of the translocation in diverse genotypes indicated that the translocation was a new source of mildew resistance that could be easily used in a breeding programme.  相似文献   

13.
The Aegilops kotschyi cytoplasm and a 1BL-1RS translocation chromosome that consists of the long arm of wheat chromosome 1B and the short arm of rye chromosome 1R were transferred to six spring common wheat cultivars by repeated backcrossing. Resistance to leaf rust race 21B conditioned by the Lr26 gene and a secalin subunit encoded by the Sec-1 gene, both on the 1RS arm, were used as the selection markers of the translocation chromosome. Five of the six cultivars used were converted to complete male steriles, whereas the remaining one, cv. Kitamiharu 48, retained normal fertility, after transfer of both the 1BL-1RS chromosome and Ae. Kotschyi cytoplasm. Conventional gene analysis suggested that Kitamiharu 48 carries an incompletely dominant fertility-restoring gene. The F1 hybrids between the male steriles and ordinary common wheat cultivars recovered fertility only at a low level, indicating that a single dose of the Rfv1 gene on the 1BS arm of wheat is insufficient for full fertility restoration under spring-sowing condition. Our results are in clear contrast to complete fertility restoration under fall-sowing condition reported by Nonaka et al. (1993). Combination of the 1BL-1RS chromosome / Ae. Kotschyi cytoplasm system with a new fertility-restoring gene discovered in Kitamiharu 48 may provide a breakthrough for spring-type hybrid wheat. This revised version was published online in August 2006 with corrections to the Cover Date.  相似文献   

14.
M. Imtiaz    M. Ahmad    M. G. Cromey    W. B. Griffin  J. G. Hampton 《Plant Breeding》2004,123(5):401-404
Stripe rust of wheat caused by Puccinia striiformis West. f. sp. tritici presents a serious problem for wheat production worldwide, and identification and deployment of resistance sources to it are key objectives for many wheat breeders. Here we report the detection of simple sequence repeat (SSR) markers linked to the durable adult plant resistance of cv. ‘Otane’, which has conferred this resistance since its release in New Zealand in 1984. A double haploid population from a cross between ‘Otane’ and the susceptible cv. Tiritea’ was visually assessed for adult plant infection types (IT) in the glasshouse and field, and for final disease severity in the field against stripe rust pathotype 106E139A+. At least three resistance loci controlled adult plant resistance to stripe rust in this population. Quantitative trait loci (QTL) mapping results revealed that two of these, one on chromosome 7DS corresponds to the durable adult plant resistance gene Yr18 and other on chromosome 5DL were contributed from ‘Otane’; while the remaining one on chromosome 7BL, was contributed from the susceptible ‘Tiritea’. Interval mapping placed the ‘Otane’‐resistant segment near the centromere of chromosome 7DS at a distance of 7 cM from the SSR marker gwm44. The stability of QTL in the two environments is discussed. SSR gwm44 is potentially a candidate marker for identifying the durable resistance gene Yr18 in breeding programmes.  相似文献   

15.
X. M. Chen    Y. H. Luo    X. C. Xia    L. Q. Xia    X. Chen    Z. L. Ren    Z. H. He    J. Z. Jia 《Plant Breeding》2005,124(3):225-228
The use of resistant cultivars is a most economical way to control powdery mildew (Blumeria graminis f.sp. tritici) in wheat (Triticum aestivum L.). Identification of molecular markers closely linked to resistance genes can greatly increase the efficiency of pyramiding resistance genes in wheat cultivars. The objective of this study was to identify molecular markers closely linked lo the powdery mildew resistance gene Pm16. An F2 population with 156 progeny was produced from the cross‘Chancellor’(susceptible) ב70281’ (resistant), A total of 45 SSR markers on chromosomes 4A and 5B of wheat and 15 SSRs on chromosome 3 of rice was used lo lest the parents, as well as the resistant and susceptible bulks: the resulting polymorphic markers were used to genotype the F2 progeny. Results indicated that the SSR marker Xgwm159, located on the short arm of chromosome 5B, is closely linked to Pm16 (genetic distance: 5.3 CM). The cytogenetical data presented in an original report, in combination with this molecular analysis, suggests that Pm16 may he located on a translocated 4A.5BS chromosome.  相似文献   

16.
To study the influence of genes from Thinopyrum intermedium on traits affecting the bread‐making quality of wheat, two derivatives from a putative disomic addition line in cultivar ‘Vilmorin 27’ were used in cytological, biochemical and molecular characterization. Cytological analysis suggested that one of the derivatives (Line‐1) had a terminal deletion involving the long arm of chromosome 1D (2n = 42, Del‐1DL”), and the other (Line‐2) was a conventional addition line, but also carried the same deletion on chromosome 1D (2n = 44, Thi”+Del‐1DL”). Amplification and sequencing of high‐molecular‐weight glutenin subunit (HMW‐GS) genes coded by the Th. intermedium chromosome in Line‐2 indicated the presence of one x‐type with an extra cysteine and four (rather than one) unique y‐type genes. Rheological studies of Line‐1 showed significantly lower dough strength compared to ‘Vilmorin 27’, confirming the recognized role of Glu‐1D coded HMW‐GSs. Line‐2 showed significantly higher dough strength compared to the background cultivar, indicating a significant potential of Th. intermedium for improvement of bread‐making quality in wheat.  相似文献   

17.
A partial amphiploid, TE-3, between Triticum aestivum cv. Chinese Spring (CS) and Thinopyrum intermedium ssp. trichophorum was characterized by cytological observation, genomic in situ hybridization (GISH), seed storage protein electrophoresis and disease resistance screening. The TE-3 plants were deeply covered with pubescence, which is characteristic of the Th. intermedium ssp. trichophorum parent. Feulgen staining of the somatic metaphases revealed that the chromosome number varied from 52 to 56. TE-3 pollen mother cells (PMCs) regularly showed two to four univalents and 25 to 27 bivalents, indicating a degree of cytological instability. Giemsa-C banding showed that the Thinopyrum chromosomes in TE-3 produced strong heterochromatin bands. GISH analysis suggested that the alien chromosomes in TE-3 consisted of eight St chromosomes, four Js chromosomes, and two J genome chromosomes, as well as two St-J translocation chromosomes. Seeds storage proteins separated by acid polyacrylamide gel electrophoresis (APAGE) and sodium dodecyl sulphate – polyacrylamide gel electrophoresis (SDS-PAGE) showed that TE-3 expressed some of Th. intermedium ssp. trichophorum specific gliadin and glutenin bands. When inoculated with stripe rust and powdery mildew isolates, TE-3 expressed resistance derived from its Thinopyrum parent. It appears that TE-3 can be used as a donor source in wheat breeding programs to introduce novel variation for quality and disease resistance.  相似文献   

18.
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.  相似文献   

19.
Potential polymorphism of an (AT)N microsatellite at the 3’end of waxy genes in bread wheat was examined. Primers were designed from a published cDNA sequence of a wheat waxy gene. Polymerase chain reaction (PCR) amplification of genomic DNA from 135 mainly Australian cultivars revealed eight alleles on chromosome 7A. This polymorphic microsatellite is a potential codominant marker for the Wx-A1 locus in breeding programmes. A distinguishable fragment was also amplified from chromosome 7D. This fragment was absent where a plant was null for the waxy gene on chromosome 7D, being a dominant marker for the Wx-D1 locus. The primers were also useful for amplifying genomic DNA from barley, rye and triticale and can be used to detect potential polymorphism in these species.  相似文献   

20.
小麦新种质CH09W83为八倍体小偃麦TAI7047与高感小麦品种晋太170杂交、回交后代衍生而来的高代选系,在苗期免疫或高抗我国白粉病菌株E09、E20、E21、E23、E26、Bg1和Bg2。为定位CH09W83中的抗病基因,将CH09W83与感病亲本杂交和回交,通过对F1、F2、F2:3和BC1代的接种鉴定和遗传分析,证实CH09W83成株期对E09的抗性由1对隐性核基因控制,暂命名为pmCH83。采用分离群体分组分析法(bulked segregant analysis, BSA),以658对SSR标记对台长29(感病)× CH09W83的F2群体分析发现,抗性基因pmCH83与SSR标记Xgpw7272、Xwmc652、Xgwm251、Xgwm193连锁,与两翼邻近标记Xwmc652和Xgwm251的遗传距离分别为3.8 cM和4.3 cM。利用中国春缺体–四体、双端体将pmCH83及其连锁标记定位在4BL染色体上。原位杂交、染色体配对及连锁标记分析结果表明,CH09W83可能是一个小麦与中间偃麦草的隐形异源渗入系。系谱和图谱位置分析表明,pmCH83很可能是来自中间偃麦草一个新的抗白粉病基因。  相似文献   

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