390份小麦-黑麦种质材料主要农艺性状分析及优异材料的GISH与FISH鉴定

将小麦近缘属植物黑麦中的优良基因导入小麦可以拓宽小麦的遗传基础,丰富小麦的遗传变异。本研究调查并分析了390份小麦-黑麦种质材料。在这390份种质材料中,6个主要农艺性状值均有较大的极差,说明其遗传多样性丰富。与10份小麦主栽品种相比,90%以上的材料具有穗长和分蘖数的显著优势,60%以上的材料具有小穗数优势,约30%的材料穗粒数和千粒重显著高于主栽品种。利用基因组原位杂交(genomic in situ hybridization,GISH)和多色荧光原位杂交(multicolor fluorescent in situ hybridization,mc-FISH)技术,对8份农艺性状优良的代表性材料进行染色体组成分析,发现3份为六倍体小黑麦(AABBRR),2份为八倍体小黑麦(AABBDDRR),1份为1RS·1BL易位系,其余2份不具有可见的黑麦染色体或染色体片段。值得指出的是,3份六倍体小黑麦与2份八倍体小黑麦所含的黑麦染色体不完全相同。八倍体小黑麦中有1对来源于黑麦的小染色体,而六倍体小黑麦中没有类似小染色体;并且,不同材料中黑麦4R染色体端部的GISH杂交带有明显差异。本研究结果为这些小麦-黑麦种质材料进一步应用于小麦育种提供了依据。     

The development of cytogenetic research at the Plant Breeding Institute Halle/Hohenthurm with special reference to aneuploidy in cereals

Summary The historical development of cytogenetic research in cereals performed at the Plant Breeding Institute of the Martin-Luther-University Halle-Wittenberg from its beginning in 1935 until 1992 is reviewed with special reference to polyploidy, alien introgression and aneuploidy.Th. Roemer founded 1935 in the framework of his Institute a Department of Mutation Research which, in 1937, was extended to a Department of Cytogenetics with R. Freisleben as the first head. Research highlights of this period were the introduction of mutation breeding, the development of autotetraploids in barley and linseed, the discovery of the crossability genes in wheat and the performance of wheat-rye crosses.The main objective in the period between 1950–1960 was the analysis of the relationships between chromosome behaviour and seed set in tetraploid rye and octoploid triticale.Since 1961 the Cytogenetics Research Group was headed by D. Mettin; he was followed by W.D. Blüthner in 1983. The research activities in this period concerning aneuploidy in rye and wheat and alien introgression are being reviewed under the following headings: Cytogenetics of rye; work with wheat aneuploids; contributions to the IR introgression into wheat; alien introgressions into wheat to improve disease resistance and grain quality; the exploitation of molecular markers.     

Confirmation of a 1A/1R Wheat-Rye Chromosome Translocation in the Wheat Variety 'Amigo'

Differential chromosome staining by using the Giemsa C- banding technique and test crosses have revealed rye chroma tin in the hexaploid wheat variety ‘Amigo’ which resulted from wheat crosses with the octoploid triticale ‘Gaucho’. The results demonstrated a pair of translocated wheat chromosomes involving the short arm of rye chromosome 1R and the long arm of the homoeologous wheat chromosome 1A (1Aq/1Rp translocation). The localization of the translocation breakpoint is supposed 10 be within the centromeric region.     

Production and Cytogenetical Analysis of a Rye-Cytoplasmic Tetraploid Triticale

A rye-cytoplasmic tetraploid triticale was found in F_s progenies of crosses between tetraploid rye‘No 1323’and hexaploid triticale‘KT 77′. In the tetraploid triticale, two complete rye genomes and two mixed wheat genomes, consisting of the chromosomes 1A. 2A, 4A, 7A, 3B, 5B, and 6B are present. The rye cytoplasm did not affect stability of rye chromosome pairing during metaphase 1, since rye chromosomes participated in pairing irregularities just as did wheat chramosomes, even on a larger scale. The fertility of F₀, plants ranged from 0 to 75.6 %, always associated with high grain shrivelling. The analyzed pairing behaviour of induced triploid hybrids from crosses between the tetraploid triticale and diploid rye indicates the presence of at least one wheat-rye translocation in one of the investigated triploid plants.     

八倍体小黑麦(Triticale)与六倍体小黑麦杂交若干问题的探讨

本工作以改进八倍体小黑麦与六倍体小黑麦的经济性状为目的,对60个杂交组合 F_1的田间出苗率、结实率、杂种后代的性状分离、新类型的形成以及细胞遗传的若干问题进行了探讨,观察到 F_1田间出苗率、结实率以八倍体为母本的杂交组合显著好于以六倍体为母本的杂交组合。由于杂种是普通小麦、硬粒小麦、黑麦三个物种种质的再度组     

黑龙江小麦麸皮膳食纤维挤压膨化—酶法改性工艺条件的优化

采用挤压膨化法和纤维素酶法对预处理后的小麦麸皮进行改性,以提高可溶性膳食纤维的含量,从而提高产品的功能性。先将预处理后的膳食纤维DF1挤压改性得到DF2,再对DF2进行纤维素酶酶解改性。结果表明,膳食纤维DF1挤压改性的最优条件为:物料含水量45%,进料速度为25 r/min,螺杆转速200 r/min,挤压温度为70-90-110-130-150℃,得到DF2的SDF含量为33.95%。膳食纤维DF2酶解改性的最优条件为:料液比为1:10,酶用量为30 U/g,酶解时间为4 h,得到最终膳食纤维成品SDF含量为72.61%。     

The Use of Monosomic Rye Addition Lines for Transferring Rye Chromatin into Bread Wheat

Hybrid plants with 21 pairs of wheat chromosomes and with a haploid rye genome were produced by backcrossing a primary octoploid triticale with its parental hexaploid wheat. Upon a second backcrossing or selfing, the rye chromosomes were eliminated rapidly. Added rye chromosomes, in varying numbers, affected the transmission rate of wheat chromosomes significantly. Loss of wheat chromosomes ranging from 0.06 to 0.35 per plant in different populations was observed. In these plants a remarkably high incidence of wheat/rye and rye/rye translocations occurred. Translocations were identified by using the C-banding technique. Among 837 analyzed plants 64 wheat/rye and 256 rye/rye translocations were identified. In different generations of backcrossing or selfing the frequency of wheat/rye translocations varied between 4.23 % and 14.67 %. All 14 rye chromosome arms were involved in translocations but with different frequencies. BC₁F₃ plants with homozygous wheat/rye translocations were isolated The results indicate that monosomic wheat/rye addition lines may be directly used as an effective means to transfer genetic material from rye into bread wheat.     

Spontaneous wheat/rye translocations from female meiotic products of hybrids between octoploid triticale and wheat

Summary Heptaploid hybrids between octoploid triticale and wheat were backcrossed as female parents with wheat to examine the rye chromosome distribution in the resultant progenies using genomic in situ hybridization (GISH). One hundred and one backcross (BC) seeds were examined and whole rye chromosome additions and substitutions, wheat/rye centric and noncentric translocations and rye telocentric chromosomes were detected. Dicentric wheat/rye translocated chromosomes were also observed. Comparisons were made with previous results on the rye chromosome distribution from male gametes of the same cross and differences were found, where in the female derived population a deficit of plants with more than two rye chromosomes was apparent relative to the anther derived population.     

Characterization of the 1B/1R translocation in wheat using water extractable protein concentrate

Summary An electrophoretic procedure was developed to obtain patterns of water soluble proteins from the endosperm halves of seeds to detect the 1B/1R translocation in wheat cultivars. The water soluble proteins were precipitated with Coomassie Brilliant Blue R-250 and separated in a 10% polyacrylamide gel with sodium dodecyl sulfate. This procedure extracted protein bands (Mr 40,000, 44,000 and 45,000) corresponding to the -secalins of the rye parent which were present only in the wheat cultivars carrying 1B/1R translocation. By simplifying extract preparation and providing clear band resolution this procedure facilitates large scale screening of wheat lines for the rye translocation. Proteins with properties of overlapping solubilities are also discussed.Abbreviations CBB - Coomassie Brilliant Blue - DDW - deionized distilled water - DTT - dithiothreitol - HMW - high molecular weight - PAGE - polyacrylamide gel electrophoresis - Mr - relative molecular mass - SDS sodium dodecyl sulfate Contribution 1569 of Agriculture and Agri-Food Canada, Research Centre, Winnipeg, Canada     

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.     

直接导入农林10号矮秆基因于八倍体小黑麦的研究

用杂交、回交方法,将农林10号的矮秆基因导入八倍体小黑麦Y1139F_7中。和预期的一样,在不涉及R组染色体重组的情况下,导入后的八倍体小黑麦种子饱满度并未下降,还略有提高。这是利用直接导入法导入普通小麦有利基因于八倍体小黑麦的第一个实例.为“未经改良的R组染色体对八倍体小黑麦的种子饱满度有干扰作用”提供了间接的证据。     

Transfer of the Glu-D1 locus encoding high molecular weight glutenin subunits 5+10 from breadwheat to diploid rye

A fragment of chromosome 1DL of breadwheat (Triticum aestivum L.) with the locus Glu-D1 encoding high molecular weight glutenin subunits 5+10 was translocated in hexaploid triticale (× Triticosecale Wittmack) to chromosome 1RL of rye (Secale cereale L.) where it replaced a corresponding fragment containing locus Sec-3 encoding rye secalins. The translocated chromosome 1R was transferred to diploid rye through backcrosses. During the transfer, at least two crossover events must have taken place that reduced the lengths of the 1DL inserts to about 5–8% of 1RL. These short inserts were selected on the basis of normal male transmission from heterozygotes and by low pairing with chromosome 1D in the F₁ hybrids with wheat, and tested by the in situ hybridization with total genomic DNA. While the wheat introgression in rye did not affect plant morphology or fertility, preliminary observations of the first population of homozygotes suggested that grain yield was lower, probably as a result of about 15% reduction of the 1000 kernel weight. The presence of a single wheat glutenin locus was insufficient to create rye with wheat-like breadmaking properties. However, relative to controls, the SDS-sedimentation value increased by about 75% and loaf volume was greater in test bakes using the procedure adapted for wheat-rye blends. Loaf volume for bread baked using the procedure for rye flour was not affected. Ryes with various glutenin subunits could be used in wheat-rye blends. This revised version was published online in July 2006 with corrections to the Cover Date.     

Chromosomal location of aluminium tolerance genes in rye

Rye is known for its high tolerance of aluminium in the soils in comparison with wheat and other cereals. To localize the major gene/ genes controlling aluminium tolerance on the rye chromosomes, four series of wheat‐rye addition lines, two sets of triticale D(R) substitution lines and several wheat/rye translocation lines were tested in experiments on seedlings grown in nutrient solutions with various concentrations of aluminium. The results indicate that the major locus responsible for Al tolerance in rye is located on the short arm of chromosome 3R. The importance of these results for controlled introgressions into cereals is discussed.     

Characterization of wheat-triticale doubled haploid lines by cytological and biochemical markers

Five wheat-triticale doubled haploid (DH) lines— M08, V209, DH220-14-2, DH696-3-4 and M16 —derived from anther culture of F₁s resulting from crosses involving hexaploid or octoploid triticale × hexaploid wheat, were characterized by cytological and biochemical markers. Cytological evidence from genomic in situ hybridization and C-banding indicated that DH lines M08 and V209 (2n= 42) each contained a pair of 1BL/1RS translocation chromosomes. DH220-14-2 (2n= 42) was also a translocated line with two pairs of chromosomes containing small fragments of rye. One of the translocation fragments carried the Sec-1R gene originating from the satellite region of 1RS; the origin of the other one remains unknown. DH696-3-4 (2n= 42) contained a 3D(3R) substitution. In M16 (2n= 44), three pairs of rye chromosomes, 3R, 4R and 6R, were present, 4R as an addition and 3D(3R) and 6D(6R) as substitutions. Biochemical, isozyme and storage protein markers confirmed the cytological conclusions. The advantages of transferring alien chromosomes or chromosome fragments into wheat and creating alien aneuploid lines by anther culture of hybrid F¹s are discussed.     

小麦-黑麦二体代换系间杂交诱导染色体易位的研究

摘 要：小麦-黑麦二体代换系间杂交,是诱导小麦-黑麦染色体易位的重要途径,有理论与应用价值。本研究利用DS1R/1D与DS5R/5A、DS6R/6A杂交,结果表明,F1减数分裂有19个二价体、4个单价体,有部分同源染色体配对和染色体易位现象;F2 对带有黑麦性状的24株普通小麦类型植株进行原位杂交检测,共检测出10株有染色体易位,易位频率为41.6%。易位株系为：06-16-7、06-16-3、06-16-5、06-16-7、06-16-8、06-17-7、0617-11、06-17-15、06-17-16、06-18-5。由于亲本选配、检测植株有一定的目的性,易位植株均表现有一定的应用价值。     

Localization of Genes in Rye that Restore Male Fertility to Hexaploid Wheat with timopheevi Cytoplasm

Four sets of wheat-rye addition lines were screened to localize genes in rye that restore male fertility to hexaploid wheat with timopheevi cytoplasm. One gene, designated Rfc3, was physically located in the distal 40 % of the long arm of chromosome 6R. No allelic variation at Rfc3 was found; normal male fertility was consistently observed in all F₁ hybrid combinations tested. A second gene, designated Rfc4, was located on the long arm of chromosome 4R. Variation between chromosomes 4R in the level of restoration was observed; fertility in hybrids ranged from 0 % to about 50 % of normal. Attempts to genetically map Rfc4 were inconclusive but suggested it was located 16.1 cM from the telomere of the long arm and at least 8.0 cM from the centromere. These restorers, particularly Rfc3, may have potential in hybrid wheat breeding programs and can be manipulated for production of male sterile triticale lines.     

Gain or loss of single chromosomes in wheat-rye addition lines and in 6x triticale detected by flow cytometry

Flow cytometric DNA analysis was used to study changes in nuclear DNA content induced by the gain or loss of chromosomes or chromosome arms in wheat-rye addition lines and in triticale. The amount of DNA present was determined by comparison with internal reference values obtained from euploid plants. The smallest difference in the DNA level which could be detected between aneuploid and euploid plants was 1.84%. Thus, it was possible to determine aneuploidy in all cases, except when very short telocentric rye chromosomes were added to wheat (addition line 1RS). The study has proved that flow cytometry is an efficient and simple way to discriminate between euploid and aneuploid plants in wheat and triticale.     

Intergeneric Transfer (Rye to Wheat) of a Gene(s) for Russian Wheat Aphid Resistance

An octoploid triticale was derived from the F, of a Russian wheat aphid-resistant rye, ‘Turkey 77’, and ‘Chinese Spring’ wheat. The alloploid was crossed to common wheat, and to ‘Imperial’ rye/‘Chinese Spring’ disomic addition lines. F₂, progeny from these crosses were tested for Russian wheat aphid resistance and C-banded. A resistance gene(s) was found to be associated with chromosome arm IRS of the ‘Turkey 77’ rye genome. A monotelosomic IRS (‘Turkey 77’) addition plant was then crossed with the wheat cultivar ‘Gamtoos’, which has the 1BL.1RS ‘Veery’ translocation. Unlike the IRS segment in ‘Gamtoos’, the ‘Turkey 77’-derived 1 RS telosome did not express the rust resistance genes Sr31 and Ar26, which could then be used as markers. From the F, a monotelosomic 1 RS addition plant that was also heterozygous for the 1BL. 1 RS translocation was selected and testerossed with an aphid-susceptible common wheat, ‘Inia 66’ Meiotic pairing between the rye arms resulted in the recovery of five euploid Russian-wheat-aphid-resistant plants. One recombinant also retained Sr31 and Lr26 and was selfed to produce translocation homozygotes.     

Gene Localization of Aspartate Aminotransferase and Endopeptidase Isozymes in Wheat and Rye Using Developmental and Organ-Specific Patterns

Wheat, rye and wheat-rye addition lines have been investigated regarding their developmental and organ-specific isozyme patterns of aspartate amino-transferase (AAT) and endopeptidase (EP). Evidence is given, that development-specific isozymes of AAT are encoded by chromosomes 3R and 4R of ‘Imperial’ rye which can be used as biochemical markers up to leaf age of 14 days. Organ-specific increase of intensity of bands for AAT in stems could be assigned to genes or alleles of chromosome 3A of ‘Chinese Spring’ wheat. For EP new markers were localized on chromosomes 4R and 6R of ‘Imperial’ rye showing variability. Utilization of these markers is possible at all developmental stages of the leaves. Mechanisms of gene regulation are discussed.     

Histological studies on the infection of triticale,wheat and rye byPuccinia recondita f.sp.tritici andP. recondita f.sp.recondita

Summary The reaction of eight triticales and of the respective wheat and rye parental lines to infection by the leaf rust fungi of wheat and rye were studied in the seedling stage. The histological observations indicated that wheat and triticale showed a typical nonhost reaction to the leaf rust of rye: sporelings of this fungus were arrested after the formation of primary infection hyphae and before the formation of extensively branched mycelium, mostly without necrosis of plant cells. The rye inbred lines were all susceptible to the rye leaf rust. The reaction of wheat and triticales to the wheat leaf rust was susceptible or resistant. The reaction of resistant lines could be early or late and complete or incomplete, but was associated with substantial necrosis of plant cells, and therefore entirely different from the nonhost reaction to rye leaf rust. In their reaction to wheat leaf rust the rye lines were similar to the resistant wheat and triticale lines. They did not show an important degree of nonhypersensitive early abortion as would be expected in a nonhost species. It appeared that genes for hypersensitive resistance in triticale may be contributed by either the wheat or the rye parental line.A screening of sixty wheat, rye and triticale lines confirmed the nonhost status of wheat and triticale to rye leaf rust and the hypersensitive or moderately susceptible reaction of rye to wheat leaf rust.