Comparative study of the structure of chromosome 1R derived from Secale montanum and Secale cereale

We produced 15 dissection lines of common wheat carrying segments of chromosome 1R of wild rye (Secale montanum) (1R^m) by the gametocidal system. Using the 1R^m dissection lines and previously established 24 dissection lines of chromosome 1R from cultivated rye (Secale cereale cv. ‘Imperial’) (1Rⁱ), we conducted cytological mapping of 97 markers that were amplified in the 1Rⁱ addition line. Sixty‐eight of the 97 markers were amplified in the 1R^m addition line. To reveal what structural differentiation occurred in chromosome 1R during domestication, we compared the cytological map of chromosome 1Rⁱ with that of chromosome 1R^m, and also with the previously published cytological map of chromosome 1R from wheat cultivar ‘Burgas 2’ (1R^B). There was one discrepancy in marker order in the satellite region between chromosomes 1Rⁱ and 1R^B, while there were four discrepancies in marker order between chromosomes 1Rⁱ and 1R^m. These results suggested that during the domestication of rye, some intrachromosomal rearrangements had occurred in chromosome 1R, although this chromosome is regarded as the most stable chromosome in the rye genome.     

Nitrogen and phosphorus uptake and utilization efficiency in D(R) substitution lines of hexaploid triticale

Two sets of disomic substitution lines, derived from the cultivars ‘Presto’ and ‘Rhino’ of triticale, with rye chromosome pairs replaced by their wheat D‐genome homoeologues, were tested in hydroponic culture for nitrogen and phosphorus uptake and utilization efficiency. The effect of a substitution on the amount of absorbed nutrients was predominantly negative and proportional to the effect on plant dry matter. Significant decreases were found for the substitutions 5D(5R), 6D(6R) of both cultivars, 2D(2R), 4D(4R) of ‘Presto’ and 3D(3R) of ‘Rhino’. On the other hand, the nitrogen utilization efficiency was significantly increased in all substitution lines, with the exception of the 1D(1R) ones. The differences in phosphorus utilization were generally positive, but less pronounced, and significant only in the lines 2D(2R) and 6D(6R). The data suggest that presence of both rye and D‐genome chromosomes is conducive for the best effect of the applied N and P fertilizers.     

小麦EST-SSR标记的开发和染色体定位及其在追踪黑麦染色体中的应用

根据小麦盐胁迫诱导和茎秆组织相关EST序列开发了81对EST-SSR引物, 其中67、46、18和61对分别在小麦、黑麦、簇毛麦和大麦基因组中稳定扩增, 在不同小麦和大麦品种间具有多态性的引物分别有22和23对。利用小麦缺体-四体系共定位了43对引物的81个位点, 其中A、B和D染色体组上分别有29、30和22个位点, 涉及除4B、3D和6D外的18条染色体。此外30对引物在黑麦基因组中具有特异扩增, 其中8对分别在黑麦1R、4R、5R和R7染色体上具有特异扩增, 7对在多条黑麦染色体具有相同扩增。这些新标记可有效用于小麦及其近缘物种的遗传作图与比较遗传研究。     

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.     

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.     

Identification of the Chromosomes in the 'Esto' Set of Rye Trisomics

The original identification of the chromosomes involved in each of the lines of the act of primary trisomics of winter rye variety ‘Esto’ does not correspond with recent results of gene localization studies. Using known morphological marker genes, N-banding and test crossing with the standard translocation tester set, a more precise identification was possible. In the nomenclature of the Triticinae, the lines can be designated as follows: A = 7R; B = 5R; C = 2R; D = 3R; E = 4R; F = 6R; G = 1R.     

Identification of Rye Chromosomes Involved in Tolerance to Barley Yellow Dwarf Virus Disease in Wheat × Triticale Hybrids

Common wheat × hexaploid triticale hybrids were produced and evaluated for tolerance to barley yellow dwarf virus disease (BYD). The BYD tolerance expression varied with wheat × triticale combination. The selection for BYD tolerance increased the recovery of tolerant genotypes in the next generations. Homozygous tolerant and susceptible lines were obtained in advanced generations. The rye chromosomes 1R, 2R, and 4R with 7R were transmitted as disomic or monosomic, disomic, and double disomic substitution to the late generations of ‘Musala’ (common wheat) בMuskox 658’ (triticale), ‘Encruzilhada’ (common wheat) בNord Kivu’ (triticale) and ‘Encruzilhada’× 12th. International Triticale Screening Nursery 267 (12ITSN267) (triticale), respectively. A clear association was established between the 1R chromosome of the ‘Muskox 658’ triticale line and the tolerance to BYDV. Results suggest that the 2R chromosome may be involved in BYD tolerance of ‘Nord Kivu’ triticale line.     

普通小麦辉县红-荆州黑麦异染色体系的选育及其梭条花叶病抗性鉴定

为发掘和利用荆州黑麦所携抗梭条花叶病基因，综合利用分子细胞遗传学与分子标记技术结合多年抗性鉴定，从高感梭条花叶病小麦地方品种辉县红与荆州黑麦杂交后代（F₇~F₉）中选育出二体异附加系5个(分别添加1R、2R、R3、5R和R7)、5RS端二体异附加系1个和多重异附加代换系2个（染色体组成分别为20’’+2R(2D)’’+4R’’和19’’+1R（1B）’’+2R（2B）’’+4R’’）。鉴定表明，双二倍体荆辉1号高抗梭条花叶病，表明黑麦抗性基因可在小麦背景中稳定表达，2R、R7二体异附加系及2个含2R的多重异附加代换系均表现高抗，推测2R和R7上可能携带抗病基因。这些材料是研究荆州黑麦抗性基因遗传及小麦抗病育种的新种质。     

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.     

Genetical Studies of Gibberellic Acid Insensitivity in Rye (Secale cereale L.)

Genetic analysis of three semi-dwarf genotypes of rye (Secale cereale L.)—‘Moskowskij Karlik’, ‘Gülzow kurz’ and ‘R 18’, which were shown to be insensitive to applied gibberellic acid (GA₃), has been carried out by using a seedling test. It could be demonstrated that all of the three genotypes are carrying recessive alleles for GA-insensitivity. Whereas the alleles of ‘Moskowskij Karlik’ and ‘R 18’ seem to have the same locus on chromosome 5R, the GA-insensitivity of ‘Gülzow kurz’ is governed by a different gene, most probably located on chromosome 7R. The relationship between the genes (alleles) for GA-insensitivity and semi-dwarfness, including the symbolization of the Gai-genes as well as their utilization in rye breeding 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.     

First-division restitution in hybrids of Langdon durum disomic substitution lines with rye and Aegilops squarrosa

Durum wheat ‘Langdon’(LDN) caused a high frequency of first‐division restitution (FDR) and partial fertility in hybrids with rye, Secale cereale L., and Aegilops squarrosa L. In order to determine the genetic control of FDR, a complete set of 14 Langdon durum D‐genome disomic substitution lines (LDNDS) was crossed with ‘Gazelle’ rye and one accession (RL5286) of A. squarrosa. The microsporogenesis and fertility of the hybrids were studied. The results showed that most of the hybrids expressed a high frequency of FDR and partial fertility. However, the hybrids of 2D(2A), 4D(4A), 5D(5B) and 6D(6B) crossed with both rye and A. squarrosa, as well as 1D(1A) with A. squarrosa, had either little or no FDR and were completely sterile. These hybrids had different types of first meiotic divisions compared with LDN control hybrids. The hybrids with 2D(2A), 4D(4A) and 6D(6B) had a high frequency of random segregation of chromosomes at the first division. The hybrids with 5D(5B), as expected, showed high homoeologous pairing. The hybrid of 1D(1A) with A. squarrosa had a high frequency of equational division at first division. These results suggest that the reduced or absent FDR in such hybrids might be related to the substitution of chromosomes with an FDR gene and poor compensation ability of the D‐genome chromosomes for their homoeologous A‐ or B‐ genome chromosomes. Cytological analysis suggested that chromosome 4A in LDN most likely carries a gene for high frequency of FDR in hybrids. In addition, some monads were observed at the end of meiosis in the hybrids of 3D(3A) and 6D(6A) crossed with rye. They were formed from FDR cells that failed to divide at second division, suggesting that the LDN 3A and 6A chromosomes might carry genes for normal second division of FDR cells in the rye crosses.     

Identification of Rye Chromosome 1R Translocations and Substitutions in Hexaploid Wheats Using Storage Proteins as Genetic Markers

Grain protein compositions of 106 advanced generation backcross lines from crosses involving ‘Amigo’ (1AL.1RS), ‘Aurora’, ‘Kavkaz’, ‘Skorospelka-35’ and ‘Sunbird’ (all 1BL.1RS) and ‘Gabo’ 1DL.1RS parents and 152 cultivars with unknown pedigree were analysed by one-dimensional SDS-PAGE. Eighty seven backcross lines and 16 cultivars carried one or other of these translocations, 2 cultivars had a 1R (1B) substitution, whereas 5 backcross lines were found to be heterogeneous for the 1BL.1RS translocation. The translocation lines were easily identified by the presence of secalins (Sec-1) controlled by rye chromosome arm IRS and a simultaneous loss of the gliadin (Gli-1) and/or triticin (Tri-1) protein bands controlled by the replaced wheat chromosome arm (1AS, 1BS or 1DS). Certain gliadins, showing no allelic variation among the genotypes analysed, were identified as markers for chromosome arms 1AS (M_r= 34 kd) and IBS (M_r= 42,33 kd). The whole chromosome substitutions 1R (1B) were recognized by scoring for the presence of Sec-1 and HMW secalin bands, Sec-3 (controlled by rye chromosome arm 1RL) and the absence of Gli-B1 and HMW glutenin subunits, Glu-B1 (controlled by wheat chromosome arm 1BL). The results have shown that protein electrophoresis provides a rapid and reliable technique for screening genotypes for these translocations and substitutions in a breeding programme.     

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     

QTLs for black-point resistance in wheat and the identification of potential markers for use in breeding programmes

Quantitative trait loci (QTLs) for black‐point resistance have been mapped in two doubled haploid‐derived wheat populations, each thought to contain unrelated sources of resistance. In the ‘Sunco’בTasman’‐derived population, QTLs were located on chromosomes 1D, 2B, 3D, 4A, 5A and 7A with each QTL explaining between 4 and 15% of the observed phenotypic variance. QTLs were contributed by both parents. In the ‘Cascades’בAUS1408’‐derived population, QTLs from ‘Cascades’ were identified on chromosomes 2A, 2D and 7A with each QTL explaining between 12 and 18% of the phenotypic variance. Several markers were identified which are promising candidates for use in marker‐assisted selection programmes. If one, two or three of these markers would have been used to select for black‐point resistance in the ‘Sunco’בTasman’ population, then with one marker 34 of 39 resistant lines, with two markers 23 of 32 and with three markers 17 of 32 would have been selected. At the same time, 67 false positives obtained by selecting with one marker are reduced to 24 by selection with two markers and to 11 by selection with three markers. Similarly, if one, two or three markers are used to select for black‐point resistance in the ‘Cascades’בAUS1408’ populations, then with one marker 25 of 31 resistant lines, with two markers 26 of 31 and with three markers 10 of 31 are selected. At the same time, 14 false positives are obtained with one marker are reduced to six by selection with two markers and no false positives are selected using three markers.     

Chromosomal Location of Genes for Gibberellic Acid Insensitivity in 'Chinese Spring' Wheat by Tetrasomic Analysis

The tetrasomics of the homoeologous groups 2, 5 and 7 of‘Chinese Spring’wheat were, together with the euploid standard, screened at the seedling stage for sensitivity to exogenously applied gibberellic acid (GA³). Whilst the seedling length of lines tetrasomic for group 2 chromosomes were taller and those for chromosomes 5A, 5D and 7D shorter in both treatments (with and without GA³) compared to the euploid control, the remaining tetrasomics — 5B, 7A and 7B — were significantly shorter than the euploids in the GA variant only. These results suggest the presence of additional genetic factors for GA insensitivity on chromosomes of the groups 5 and 7 of hexaploid wheat. This corresponds with the localization of GA insensitive dwarfing genes on the homoeologous chromosomes 5R and 7R in diploid rye.     

Hexaploid triticales from hybrids of 'Langdon' durum D-genome substitutions with 'Gazelle' rye

The formation of unreduced gametes in some hybrids between disomic D‐genome substitutions (DS) of durum wheat cv.‘Langdon’ and rye provides a convenient approach for the rapid introduction of D‐genome chromosomes into hexaploid triticale. Meiotic pairing at metaphase I and seed fertility in spontaneous and colchicine‐induced amphidiploids derived from F₁ hybrids between a set of ‘Langdon’ DS and ‘Gazelle’ rye were analysed. The purpose was to determine the effects of the substitution of D‐genome chromosomes for their A‐ and B‐genome homoeologues on hexaploid triticale and to select stable disomic D‐genome substitutions of hexaploid triticale. The results showed that the disomic substitutions with D‐genome slightly increased the frequency of univalents (1.0‐3.13) compared with the ‘Langdon’ control primary hexaploid triticale (0.76). Substitutions 2D(2A) and 3D(3B) were partly desynaptic. The substitutions 1D(1A), 1D(1B) and 7D(7B) exhibited high seed fertility but the others had decreased fertility. Except for 2D(2A), 5D(5A), 3D(3B) and 5D(5B), 10 of the 14 possible hexaploid triticale D‐genome disomic substitutions have been obtained. The results suggest that the poor compensation ability of some D‐genome chromosomes for their homoeologous A‐ and B‐genome chromosomes is a major factor affecting meiotic stability and fertility in the hexaploid triticale D‐genome substitutions.     

Aneuploid and other cytological tester sets in rye

Summary Cytological tester sets include series of aneuploids (nullisomics, monosomics, trisomics of different types, tetrasomies), series of rearranged chromosomes (translocations, inversions, duplications, deficiencies) and series of chromosomes recognizable by specific microscopically visible markers (C- or other banding, molecular markers). In rye, only a few (mainly tertiary and telocentric) monosomics and no viable nullisomics have been found. Several sets of primary trisomics and some telocentric sets, usually not fully complete, have been developed, but few are still available for gene localization. A few tertiary trisomics have been derived from translocation heterozygotes. Extensively used are different sets of additions of rye chromosomes to wheat. A relatively widely distributed set of marked chromosomes is the Wageningen translocation tester set, complemented with translocations from different other institutions. A disadvantage of rye translocations is insufficient heterozygote semisterility. Series of otherwise rearranged chromosomes have not been reported. Sets of lines with chromosomes conspicuously differing from the standard C-banding pattern have been obtained. Molecular markers are available for most rye chromosome, but lack of heterozygosity, necessary for classification after in situ hybridization is a restriction for use as cytological testers. In the cases of most translocations, C-banding and in situ molecular markers, each separate plant in a segregating population must be screened cytologically, whereas with aneuploid markers or with translocations having sufficient heterozygote semisterility, analyzing segregations is sufficient.     

Aneuploid and other cytological tester sets in rye

Summary Cytological tester sets include series of aneuploids (nullisomics, monosomics, trisomics of different types, tetrasomics), series of rearranged chromosomes (translocations, inversions, duplications, deficiencies) and series of chromosomes recognizable by specific microscopically visible markers (C-or other banding, molecular markers). In rye, only a few (mainly tertiary and telocentric) monosomics and no viable nullisomics have been found. Several sets of primary trisomics and some telocentric sets, usually not fully complete, have been developed, but few are still available for gene localization. A few tertiary trisomics have been derived from translocation heterozygotes. Extensively used are different sets of additions of rye chromosomes to wheat. A relatively widely distributed set of marked chromosomes is the Wageningen translocation tester set, complemented with translocations from different other institutions. A disadvantage of rye translocations is insufficient heterozygote semisterility. Series of otherwise rearranged chromosomes have not been reported. Sets of lines with chromosomes conspicuously differing from the standard C-banding pattern have been obtained. Molecular markers are available for most rye chromosome, but lack of heterozygosity, necessary for classification afterin situ hybridization is a restriction for use as cytological testers. In the cases of most translocations, C-banding andin situ molecular markers, each separate plant in a segregating population must be screened cytologically, whereas with aneuploid markers or with translocations having sufficient heterozygote semisterility, analyzing segregations is sufficient.