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[Cytogenetic analysis of hybrids resistant to yellow rust and powdery mildew obtained by crossing common wheat (Triticum aestivum L., AABBDD) with wheat of the Timopheevi group (AtAtGG)].

The karyotypes of 47 hybrid lines obtained from crosses of common wheat Triticum aestivum L. (cv. Rodina and line 353) with Triticum timopheevii Zhuk, (AtAtGG) and related species T. militinae Zhuk. et Migusch. (AtAtGG) and T. kiharae Dorof. et Migusch. (AtAtGGDsqDsq) were analyzed by C-banding. Most lines were resistant to yellow rust and powdery mildew. The introgression of alien genetic material to the common wheat genome was realized via substitutions of complete At-, G-, and D-genome chromosomes, chromosome arms, or their fragments. The pattern of chromosome substitutions in resistant lines differed from that in introgressive hybrids selected for other traits. Substitutions of chromosomes 6G, 2At, 2G, and 5G were revealed in 31, 23, 18, and 13 lines, respectively. Substitutions of chromosomes 4G-, 4At, and 6At were not observed. In 15 lines, a 5BS. 5BL-5GL translocation was identified. High frequency of substitutions of chromosomes 2At, 2G, 5G, and 6G indicate that they may carry the resistance genes and that they are closely related to the respective homoeologous chromosomes of common wheat that determines their high compensation ability.

Fungi↗

[Genetic analysis of anthocyanin of the anthers and culm pigmentation in common wheat].

Anthocyanin pigmentation of various organs develops during plant ontogeny in response to adverse and damaging abiotic and biotic stressors (environmental factors). Using the monosome method, the genes responsible for anther and culm anthocyanin pigmentation (Pan1 and Pc2, respectively) were localized to 7D chromosome in introgressive lines from crosses between common wheat Triticum aestivum L. and the species Triticum timopheevii Zhuk. Genetic analysis of ten common wheat genotypes using testers carrying genes Pan1, Pn1, and Pn2 showed that these genotypes contained Pan1 and Pn2 genes. Visual examination of plants from 70 and 76 varieties of respectively winter and spring common wheat revealed anthocyanin pigmentation of anthers and culms in 36 varieties. Pan1 and Pn2 genes were presumably introduced into common wheat from Aegilops tauschii (Fig.) Tzvel., a donor of the D genome.

Chromosomes, Plant↗

Genetic induction of chromosomal rearrangements in barley chromosome 7H added to common wheat.

Chromosome 2C of Aegilops cylindrica induces chromosomal rearrangements in alien chromosome addition lines, as well as in euploid lines, of common wheat. To induce chromosomal rearrangements in barley chromosome 7H, reciprocal crosses were made between a mutation-inducing common wheat line that carries a pair of 7H chromosomes and one 2C chromosome and a 7H disomic addition line of common wheat. Many shrivelled seeds were included in the progeny, which was an indication of the occurrence of chromosome mutations. The chromosomal constitution of the viable progeny was examined by FISH (fluorescence in situ hybridization) using the barley subterminal repeat HvT01 as a probe. Structural changes of chromosome 7H were found in about 15% of the progeny of the reciprocal crosses. The aberrant 7H chromosomes were characterized by a combination of N-banding, FISH and genomic in situ hybridization. Mosaicism for aberrant 7H chromosomes was observed in seven plants. In total, 89 aberrant 7H chromosomes were identified in 82 plants, seven of which had double aberrations. More than half of the plants carried a simple deletion: four short-arm telosomes, one long-arm telosome, and 45 terminal deletions (23 in the short arm, 21 in the long arm, and one involving both arms). About 40% of the aberrations represented translocations between 7H and wheat chromosomes. Twenty of the translocations had wheat centromeres, 12 the 7H centromere, with translocation points in the 7HS (five) and in the 7HL (seven), and the remaining four were of Robertsonian type, three involving 7HS and one with 7HL. In addition, one translocation had a barley segment in an intercalary position of a wheat chromosome, and two were dicentric. The breakpoints of these aberrations were distributed along the entire length of chromosome 7H.

Chromosome Aberrations↗

[Molecular study and C-banding of chromosomes in common wheat alloplasmic lines obtained from the backcross progeny of barley-wheat hybrids Hordeum vulgare L. (2n = 14) x Triticum aestivum L. (2n = 42) and differing in fertility].

We studied common wheat alloplasmic lines differing in fertility traits, which had been obtained from the backcross progeny of barley-wheat hybrids Hordeum vulgare L. (2n = 14) x Triticum aestivum L. (2n = 42), using molecular analysis and chromosome C-banding. It was found that the nuclei of all alloplasmic lines studied, regardless of their fertility traits, contained only the common wheat chromosomes (2n = 42). The formation of line L-79(10)(3)F6, stable for self-fertility, from line L-79(10)(3)F6 was accompanied by changes of the proportions of simple sequence repeats of the parental common wheat varieties in the nuclear genome. The presence of barley genome fragments in line accessions with incomplete self-fertility was shown by RAPD. Heteroplasmy for mitochondrial genome loci was detected in these lines with the use of primers specific to the tMet-18S-5S repeat of mitochondrial ribosomal genes.

Chimera↗

[Analysis of inheritance of morphological and biochemical characters introgressed into common wheat from Aegilops speltoides Tausch].

Genetic control of some morphological traits and the gliadin composition were examined in plants of two lines of common wheat carrying genes introgressed from the wild diploid cereal Aegilops speltoides. Leaf hairiness was shown to be controlled by a single introgressed dominant gene that was not allelic to the known common wheat gene Hl1. Waxlessness of the whole plant is controlled by the introgressed from Ae. speltoides inhibitor gene allelic to gene W1 located on chromosome 2B. This gene was epistatic to the introgressed gene controlling spike waxlessness. The introgressed gene of spike color was shown to be allelic to Rg1 located on chromosome 1B of common wheat. However, the former gene proved to be linked to an allele of the Gli-B1 locus other than in wheat.

Alleles↗

[RAPD-PCR analysis of the variability of spring common wheat cultivar genomes and their androclinal double haploid form].

Based on RAPD-PCR analysis with 15 primers including those homologous to particular loci, the level of genetic polymorphism in the collection of spring common wheat genotypes and their androclinal double haploid (ADH) lines was determined. Intraspecific polymorphism of the original wheat forms was 20%. By the absence of polymorphism in the molecular patterns of ADH lines and original forms, it was shown that, under the conditions used, no genetic changes in the genomic DNA of spring common wheat in anther culture occurred. Thus, the technology of direct in vitro androgenesis does not lead to genome rearrangements and may be used for rapid production of pure lines of such a complex allopolyploid as spring common wheat.

Base Sequence↗

[Transfer of a rye small chromosomal segment with powdery mildew-resistant gene(s) into common wheat (Triticum aestivum L.)].

The advanced progeny lines (BC1F5) from the monosomic addition lines between common wheat cultivar Mianyang 11, which is highly susceptible to powdery mildew, and an inbred rye line R12 were analyzed for selection of wheat-rye translocations. Based on a rye-specific repetitive sequence of pSc20H, which spread over all chromosomes of rye but did not existed in wheat, a set of PCR primer was designed and used to identify the rye chromosome segments in wheat. From 300 of the BC1F5 progeny lines 70 were found to contain chromosome composition of rye. An advanced line, 96II691-830-98, originated from 6R monosomic addition line was observed to be immune to powdery mildew, different from its wheat parent Mianyang 11. A small segment of rye chromosome at telomere in a pair of wheat chromosome in the line was found by means of GISH. The results indicated that a small segment of rye chromosome 6R carrying the gene(s) for resistance to powdery mildew has been transferred into common wheat. In the progeny of monosomic addition lines a high frequency of wheat-alien species translocation with various segments of chromosomes could be found by application of both PCR and GISH technique.

Chromatin↗

[Recombination frequency in the locus Gli-D1 of common wheat T. aestivum L].

The recombination frequency at the gliadin locus Gli-D1 of common wheat was determined by the maximum likelihood method. Recombination was observed between the gene encoding the fastest omega-component of the allele Gli-D1j, and the genes encoding the other omega-gliadins of this allele. The frequency of recombination was 0.65 +/- 0.18% for the cross between the near-isogenic lines of winter common wheat with respect to gliadin loci Gli-D1-4 and Gli-B1-3 and 0.78 +/- 0.45% for the cross between the varieties Yunnat and B-16.

Alleles↗

[Studies on fertility genes and its genetic characters in D2-type CMS lines of common wheat].

The kinds of fertility genes and its genetic characters for D2-type CMS lines of common wheat were studied, the results showed: (1) For D2-type CMS line, there was wide restoring sources and high digree of restoration in common wheat varieties (the restoring degree of 33.61% varieties exceeded 50%), and new CMS lines were easily bred (25.21% varieties could maintain male sterility). These characters indicated that D2-type CMS line was higher value in applied study, compared with T, K, V-type CMS lines. (2) There were two forms of nuclear genotype for D2-type CMS lines, namely A1(sterile gene) and A2(sterile gene + inhibiting gene). In nucleus of restorer lines, the fertility genotype was conditioned by 6 forms: C1(major restorer gene), C2(major restorer gene + minor restorer gene), C3(minor restorer gene), C4(major restorer gene + inhibiting gene), C5(major restorer gene + minor restorer gene + inhibiting gene), C6(minor restorer gene + inhibiting gene). The genetic expression of fertility genes was affected by environmental factors. The basic model of effective combination was A1 + C1, A1 + C2, A2 + C2. (3) The allelic restorer-genes were characterized by incomplete dominance and the nonallelic restorer-genes were characterized by additive effect, which was the important basis of breeding good restorer lines.

Fertility↗

Regulation by Vrn-1/Fr-1 chromosomal intervals of CBF-mediated Cor/Lea gene expression and freezing tolerance in common wheat.

Vrn-1/Fr-1 chromosomal regions of common wheat possess major QTLs for both winter hardiness (Fr) and vernalization requirement (Vrn). The Vrn-1/Fr-1 intervals are assigned to long arms of the homologous group 5 chromosomes. To investigate the role of the Vrn-1/Fr-1 intervals on the low-temperature (LT) inducibility of wheat Cor/Lea genes and its putative transcription factor gene Wcbf2, LT response of these genes was monitored using near-isogenic lines (NILs) for the Vrn-1 loci. The Wcbf2 transcript accumulated rapidly after LT treatment and remained at a high level in lines without any dominant Vrn-1 alleles. By contrast, the Wcbf2 transcript level was greatly reduced in lines carrying the Vrn-1 alleles. The Vrn-1 NILs accumulated much lower amounts of Cor/Lea transcripts and COR/LEA proteins than the non-carrier line. The observed patterns and levels of gene expression, particularly in the Vrn-A1 NIL, agreed with the higher sensitivity to freezing damage in this line than in the non-carrier line. Up-regulation of the expression of the WAP1 gene, a candidate of the Vrn-1 loci, was much delayed in the non-carrier line than all the NILs carrying the Vrn-1 loci. Neither positive nor negative relationships were found between the WAP1 expression and the Cbf2/Cor/Lea expression. These results support the intimate relationship between the Cbf2/Cor/Lea expression and the level of freezing tolerance, and suggest that a functional Fr-A1 allele linked to the vrn-A1 allele, instead of the vernalization gene itself, plays a major role in regulating the CBF-mediated Cor/lea gene expression in wheat.

Adaptation, Physiological↗

[Effect of fusococcin on the genome of common wheat].

The effect of fusicoccin on the common wheat genome (cv. Mironovskaya 808) during early phases of seed germination was studied. It was shown that fusicoccin: (1) increased the number of cells with one or two nucleoli and decreased the proportion of cells containing three and four nucleoli; (2) enhanced the total volume of nucleoli per nucleus at a concentration of 0.68 mg/l; (3) did not activate additional rRNA genes on chromosomes 1B and 6B; (4) did not activate the latent nucleolus organizer regions on chromosomes of genome B; (5) induced associations of nucleolus organizer regions on B-genome chromosomes; (6) significantly enhanced mitotic activity in apical meristem of seedling root tips and promoted the first peak of mitoses; the effect disappeared after 44 h of seed imbibition; (7) in contrast to gibberellin, did not synchronize cell division; (8) did not cause chromosome and chromatid aberrations and increase the frequency of sister chromatid exchanges at physiologically active concentrations. Presumable mechanisms of fusicoccin-induced activation of rRNA genes are discussed in relation to the identification of the fusicoccin receptor belonging to the GF14 proteins with an intracellular binding site, to the detection of endogenous fusicoccin in plants in vivo, and to fusicoccin-induced activation of gene transcription.

Cell Nucleolus↗

Genetics of growth habit (spring vs winter) in common wheat: confirmation of the existence of dominant gene Vrn4.

The number of dominant Vrn genes in common wheat, Triticum aestivum L., is estimated. Data were obtained supporting Pugsley's and Gotoh's data on the presence of a dominant gene Vrn4 in near-isogenic line 'Triple Dirk F'. The presence of a dominant gene Vrn4 in line 'Gabo-2' of cultivar 'Gabo', which was used by Pugsley as a donor of the gene Vrn4 for the near-isogenic line 'Triple Dirk F', was also confirmed. The Vrn2 and Vrn4 relationship and their chromosomal location are discussed. It was demonstrated that the dominant Vrn8 gene which was introgressed from Triticum sphaerococcum to common wheat by Stelmakh and Avsenin is allelic to Vrn4. While genes Vrn6(sc) and Vrn7(sc) which were introgressed from rye, Secale cereale L., by the above-mentioned authors are not allelic to the genes Vrn1, Vrn2, Vrn3 and Vrn4.

Alleles↗

Molecular characterization of durum and common wheat recombinant lines carrying leaf rust resistance (Lr19) and yellow pigment (Y) genes from Lophopyrum ponticum.

Chromosome 7E from Lophopyrum ponticum carries a valuable leaf rust resistant gene designated Lr19. This gene has not been widely used in common wheat breeding because of linkage with the yellow pigment gene Y. This gene tints flour yellow, reducing its appeal in bread making. However, a high level of yellow pigment is desirable in durum wheat breeding. We produced 97 recombinant chromosomes between L. ponticum transfer 7D.7E#1 and its wheat homoeologues, using the ph1b mutation that promotes homoeologous pairing. We characterized a subset of 37 of these lines with 11 molecular markers and evaluated their resistance to leaf rust and the abundance of yellow pigment. The Lr19 gene was mapped between loci Xwg420 and Xmwg2062, whereas Y was mapped distal to Xpsr687, the most distal marker on the long arm of chromosome 7. A short terminal 7EL segment translocated to 7A, including Lr19 and Y (line 1-23), has been transferred to durum wheat by backcrossing. The presence of this alien segment significantly increased the abundance of yellow pigment. The Lr19 also conferred resistance to a new durum leaf rust race from California and Mexico that is virulent on most durum wheat cultivars. The new durum lines with the recombinant 7E segment will be useful parents to increase yellow pigment and leaf rust resistance in durum wheat breeding programs. For the common wheat breeding programs, we selected the recombinant line 1-96, which has an interstitial 7E segment carrying Lr19 but not Y. This recombinant line can be used to improve leaf rust resistance without affecting flour color. The 7EL/7DL 1-96 recombinant chromosome did not show the meiotic self-elimination previously reported for a 7EL/7BL translocation.

Basidiomycota↗

[Studies of the genetic characters of four isonucleus-alloplasmic lines of common wheat] [In Process Citation]

NC-hybird D2-CA8057 with D2-type cytoplasm and the nucleus of common wheat CA8057, cytoplasmic male-sterile (CMS) line msD2-CA8057 resulting from the variation of D2-type cytoplasm and CMS line msA-CA8057 resulting from the variation of CA8057 cytoplasm were bred. The genetic characters of the four isonucleus-alloplasmic line were studied, and the main results are as follows: (1) there were good genetic effects of cytoplasms on productive and qualitative characters of common wheat, the alloplasmic lines had the potential of NC-heterosis. (2) CMS line msD2-CA8057 and msA-CA8057 had different degenerative characters of anthers and pollen grains, msD2-CA8057 degenerated from the later uninucleus-pollen stage to the binucleus-pollen stage and the pollen grains had starch grains, msA-CA8057 degenerated at the later uninucleus-pollen stage and the pollen grains had no starch grains. (3) msD2-CA8057 and msA-CA8057 were easily maintained but different in the fertility behaviors, the former had wider restoring sources and high digree of restoing, the latter had few restoring sources but there were strains with high restoring ability. The application value of alloplasmic lines and the two new CMS-patterns were evaluated from various aspects, the possible reasons of cytoplasmic variation and the relativity between degenerative pattern of pollen grain and the fertility behavior were discussed.

Journal Article↗

Inheritance of the light intensity response in spring cultivars of common wheat.

The effects of low/high light intensities and day length on ear emergence time in climatic chambers were studied in 12 common wheat (Triticum aestivum L.) cultivars of different ecogeographical origin. Low light intensity (LI) affected the time to ear emergence in all the wheat cultivars of both the photoperiod sensitive and insensitive genotypes, increasing the number of days to ear emergence (DEE). Based on the increase in DEE, we chose samples with different light intensity responses among the cultivars and analyzed their F2 hybrids to see if they were segregating. Taken together, the data for the F2 plants and test cross showed that the strong response to light intensity is a recessive trait and that the parental cultivars differ by the two genes controlling the LI response in common wheat. Besides heading time, low LI increased the number of days to tillering in all the cultivars except Pitic 62, but short day affected the period to tillering less than low LI. The symbol Rli (the response to light intensity) is suggested to designate the genetic control of the response to LI in wheat. Thus, the response to LI may influence the adaptability to changing environmental conditions and yield of wheat cultivars.

Genes, Plant↗

Chromosome painting in plants: in situ hybridization with a DNA probe from a specific microdissected chromosome arm of common wheat.

We report here on the successful painting of a specific plant chromosome within its own genome. Isochromosomes for the long arm of chromosome 5 of the wheat B genome (5BL) were microdissected from first meiotic metaphase spreads of a monoisosomic 5BL line of the common wheat Triticum aestivum cv. Chinese Spring. The dissected isochromosomes were amplified by degenerate oligonucleotide-primed PCR in a single tube reaction. The amplified DNA was used as a complex probe mixture for fluorescent in situ hybridization on first meiotic metaphase spreads of lines carrying 5BL as a distinctive marker. Hybridization signals were observed, specifically, along the entire 5BL. In some of the cells, labeling was also detected in two bivalents, presumably those of the 5B "homoeologues" (partial homologues) found in common wheat (5A and 5D). The probe also revealed discrete domains in tapetal nuclei at interphase, further supporting the probe's high specificity. These data suggest that chromosome and homoeologous group-specific sequences are more abundant in 5BL than genome-specific sequences. Chromosome-painting probes, such as the one described here for 5BL, can facilitate the study of chromosome evolution in polyploid wheat.

Base Sequence↗

Isolation and characterization of SSR sequences from the genome and TAC clones of common wheat using the PCR technique.

We have developed the 2-step PCR method, a kind of suppression PCR procedure, to isolate simple sequence repeats (SSRs) from common wheat (Triticum aestivum L.) in a more convenient manner. This system requires neither genomic library screening nor the SSR-enrichment procedure. As a result, we designed 131 primer pairs based on isolated SSRs from not only genomic DNA, but also transformation-competent artificial chromosome (TAC) clones. It has been demonstrated that 34 of the 131 SSR markers developed were polymorphic among 8 wheat lines. Four of 34 polymorphic SSR markers were derived from TAC clones, indicating that this method could be applied to the targeted development of unique SSR markers in large genomic DNA libraries such as those composed of bacterial artificial chromosomes (BACs). A considerable number of isolated SSR clones had similarities with part of several long terminal repeats of retrotransposons (LTR-RTs) identified in various Triticeae genome sequences. Most of those SSRs showed smear amplification profiles, suggesting that a considerable number of dysfunctional SSRs originating from repetitive DNA components, especially LTR-RTs, might exist in the common wheat genome.

Base Sequence↗

Characterization of two non-homoeologous nuclear genes encoding mitochondrial alternative oxidase in common wheat.

Mitochondrial alternative oxidase (AOX) is the terminal oxidase responsible for cyanide-insensitive and salicylhydroxamic acid-sensitive respiration. We have isolated two non-homoeologous genes (Waox1a and Waox1c) encoding AOX proteins from common wheat (Triticum aestivum L.). These two genes were orthologous to rice AOX1a and AOX1c, and their exon/intron structure was conserved, as it is in most other plant AOX genes. Southern blot analysis indicated that both Waox1a and Waox1c were located in at least three homoeologous loci and that additional AOX genes with lower homology were present in the genome of common wheat. The Waox1a and Waox1c loci were respectively assigned to the homoeologous group 2 and 6 chromosomes. The steady-state level of Waox1a and Waox1c transcripts increased under cold stress, while only that of Waox1a was increased by cyanide treatment.

Amino Acid Sequence↗