Homeologous proteins synthesis controlled by homeologous chromosomes in wheat

Two homeologous proteins have been isolated from the endosperm of common wheat (genomes ABD). Synthesis of these two proteins is controlled by the homeologous chromosomes 7B and 7D respectively. However, Aegilops speltoides, the more generally accepted B genome donor, does not synthesize the 7B protein

Chromosomal location of a gene that controls sterol esterification in Triticum aestivum L.

A previously described D genome locus (Pln) that controls sterol esterification in the wheat kernel has been assigned to the short arm of chromosome 7 D by comparison of the steryl ester phenotype of euploid kernels of Triticum aestivum variety Chinese Spring with those of the compensated nulli-tetrasomic lines and the 7 D S ditelosomic. Palmitate is the predominant ester in all but the 7 D nullisomic combinations, which have linoleate as the main ester. These lines also show a marked decrease in sterol esterification and a two-fold increase in free sterol, indicating that chromosomes 7 A and 7 B do not compensate for the loss of esterification capacity associated with 7 D

Effects of n-butanol and filipin on membrane permeability of developing wheat endosperm with different sterol phenotypes.

Sterols are considered structural components of higher plant membranes on the basis of their presence in membrane-containing subcellular fractions [1—3], their effect on plant membrane permeability when added exogenously [4,5] and the sensitivity of plant cells to the polyene antibiotic filipin [6—8], which action is known to depend on the presence of sterols in the membrane (see [8]). Our recent finding of a gene that controls the free sterol level of developing wheat endosperm [9—11 ] allows to investígate whether endogenous sterol modifies membrane permeability in the same way as that added externally. We report here on the effect of «-butanol and filipin on the leakage properties of developing wheat endosperms with different genetically determined free sterol levéis

Eyespot resistance gene Pch-1 from Aegilops ventricosa is associated with a different chromosome in wheat line H-93-70 than the resistance factor in "Roazon" wheat

The hexaploid wheat line H-93-70 carries a gene (Pch-1) that has been transferred from the wild grass Aegilops ventricosa and confers a high degree of resistance to eyespot diesease, caused by the fungus Pseudocercosporella herpotrichoides. Crosses of the resistant line H-93-70 with the susceptible wheat Pané 247 and with a 7D/7Ag wheat/Agropyron substitution line were carried out and F2 kernels were obtained. The kernels were cut transversally and the halves carrying the embryos were used for the resistance test, while the distal halves were used for genetic typing. Biochemical markers were used to discriminate whether the transferred Pch-1 gene was located in chromosome 7D, as is the case for a resistance factor present in Roazon wheat. In the crosses involving Pané 247, resistance was not associated with the 7D locus Pln, which determines sterol ester pattern (dominant allele in H-93-70). In the crosses with the 7D/7Ag substitution line, resistance was neither associated with protein NGE-11 (7D marker), nor alternatively inherited with respect to protein C-7 (7Ag marker). It is concluded that gene Pch-1 represents a different locus and is not an allele of the resistance factor in Roazon whea

Loss of redundant gene expression after polyploidization in plants

Based on chromosomal location data of genes encoding 28 biochemical systems in allohexaploid wheat,Triticum aestivum L. (genomes AABBDD), it is concluded that the proportions of systems controlled by triplicate, duplicate, and single loci are 57%, 25%, and 18% respectively

Resistance to eyespot (Pseudocercosporella herpotricoides) and distribution of biochemical markers in hexaploid lines derived from double cross (Triticum turgidum x Aegilops ventricosa) x T. aestivum

There are not good intraspecific sources of resistance to the eyespot disea se of wheat, aaused by Cercosporella herpotrichoides Fvon . The -ínterspecifia transfer of genes for resistanoe from Aegitops ventricosa into hexaploid wheat has been only partially achieved, because the degree of resistanoe attained is not as high as that of the donor. We report here on the transfer of resistanoe in a double oross (Triticum turgidum var. rubroatrwv H-1-1 x Ae.ventricosa AP-D x T.aestivum cv. Almatense H-10-15. The high level of resistanoe in a high proportion of the lines strongly suggests a simple genetic control for this oharacter (possibly by one major gene). The gene(s) responsible for resistanoe in the selected lines must be associa ted with the D genome of Aegilops ventricosa on the basis of a detailed study of the distribution of biochemioal markers in the H-93 lines. These results do not exelude that genes with similar effeets might be looated in the M° genome

Dithiothreitol increases f3-glucuronidase accumulation in transformed tobacco (Nicotiana tabacum) protoplasts without altering their viability or the synthesis and export of cellular proteins

The effect of dithiothreitol (DTT) on the expression of the β-glucuronidase (GUS) reporter gene under the control of the CaMV-35 S promoter has been investigated by radioactive labelling and immunoprecipitation of the enzyme in protoplasts from stably transformed tobacco plants and compared with that observed in protoplasts transiently expressing the same gene construct. An increase in net accumulation of GUS during the culture period in response to externally added DTT (2 mm) was observed both in protoplasts from transformed tobacco plants and in electroporated protoplasts. DTT had no effect on rate of degradation of the mature GUS protein, as shown in a pulse-chase experiment. Relevant aspects of protoplast physiology, such as viability, synthesis of 35S-labelled cellular proteins, or synthesis and export of pathogenesis-related proteins (one putative chitinase and two 1,3-β-glucanases) were not affected by the reducing reagen

Genetic transfer of resistance to powdery mildew and of an associated molecular marker from Aegilops ventricosa to hexaploid wheat.

Resistance to powdery mildew, caused by the fungus Erysiphe graminis f.sp. tritici, has been transferred from Aegilops ventricosa (genomes DvMv) to hexaploid wheat (Triticum aestivum, ABD). In two transfer lines, H-93-8 and H-93-35, the resistance gene was linked to a gene encoding protein U-1, whereas one line, H-93-33, was resistant but lacked the molecular marker, and another line, H-93-1, was susceptible but carried the gene for U-1, indicating that the original Mv chromosome from Ae. ventricosa, carrying the two genes, had undergone recombination with a wheat chromosome in the last two lines

Biochemical and cytological characterization of wheat/Aegilops ventricosa addition and transfer lines carrying chromosome 4MV

The gene encoding a variant of alcohol dehydrogenase, Adh-, has been found to be associated with the chromosome of the Mv genome which is present in type 9 wheat/Aegilops ventricosa addition line, to which the genes for protein CM-4 and for a phosphatase variant, Aph-v, had been previously assigned. Transfer line H-93-33, which has 42 chromosomes and has been derived from the cross (Triticum turgidum x Ae. ventricosa) x T. aestivum, carries genes encoding all three biochemical markers. Linkage between these genes has been demonstrated by analysis of individual kernels of the F2 (H-93-33 x T. aestivum cv. Almatense H-10-15). A study of the hybrids of line H-93-33 with T. aestivum H-10-15 and with the 4DS ditelosomic line has confirmed that, as suspected, the linkage group corresponds to chromosome 4Mv from Ae. ventricosa. Additionally, it has been found that the previously reported resistance of line H-93-33 to powdery mildew (Erysiphe graminis) is also linked to the biochemical markers; this indicates that either the gene responsible for it is different from that in lines H-93-8 and H-93-35, or that a translocation between two different Mv chromosomes has occurred in line H-93-33

Morocco as a possible domestication center for barley: biochemical and agromorphological evidence.

The distribution of genetic variants of a group of low molecular weight, chloroform-methanol soluble proteins (CM proteins), among Moroccan and non-Moroccan accessions of Hordeum spontaneum and among selections from several Moroccan landraces of H. vulgare and cultivars of the same species with widespread European origin, suggests that domestication of barley might have taken place in Morocco. An agromorphological characterization of the H. spontaneum accessions further supports this hypothesis. The possible Moroccan origin of the French cultivar Hatif de Grignon and of several Spanish 6-rowed barleys is also presented