Summary Since the mid-1940's, barley cultivars grown in the northern Great Plains of the USA and Canada have been resistant to stem rust caused byPuccinia graminis f. sp.tritici. This durable resistance is largely conferred by a single gene,Rpg1, derived from a single plant selection of the cultivar Wisconsin 37 and an unimproved Swiss cultivar. At the seedling stage, barley genotypes withRpg1 generally exhibit low mesothetic reactions at 16–20° C and slightly higher mesothetic reactions at 24–28° C to many stem rust pathotypes. This resistance is manifested by a low level of rust infection and mostly incompatible type uredia on adult plants.Rpg1 reacts in a pathotype-specific manner since some genotypes ofP. g. f. sp.tritici are virulent on cultivars carrying this gene in the field. Several factors may have contributed to the longevity of stem rust resistance in barley, a) since barley is planted early and matures early, it can sometimes escape damage from stem rust inoculum carried from the south; b) one or more minor genes may augment the level of resistance already provided byRpg1; c) the cultivation of resistant wheat cultivars and eradication of barberry have reduced the effective population size and number of potential new pathotypes ofP. g. f. sp.tritici, respectively; and d) virulent pathotypes ofP. g. f. sp.tritici andP. g. f. sp.secalis have not become established. This situation changed in 1989 when a virulent pathotype (Pgt-QCC) ofP. g. f. sp.tritici became widely distributed over the Great Plains. However,Rpg1 may still confer some degree of resistance to pathotype QCC because stem rust severities have been low to moderate and yield losses light on barley cultivars carrying the gene during the last four seasons (1989–1992). Several sources of incomplete resistance to pathotype QCC have been identified in barley. To facilitate the transfer of resistance genes from these sources into advanced breeding lines, molecular marker assisted selection is being employed. 相似文献
A review of research at the Scottish Crop Research Institute (SCRI) on the effects of semi-dwarfing genes on salt tolerance
in barley is given. Work began in1993 with the fortuitous and unexpected result that the cultivar ‘Golden Promise’ showed
considerable tolerance to salt. Golden Promise is a gamma-ray induced semi-dwarf mutant of the cultivar ‘Maythorpe’. The parent
and mutant cultivars are presumed to be isogenic, but show significant differences in their responses to salt stress. The
positive and pleiotropic effects of the mutant gene, commonly known as GPert were found to be effective in a number of genetic backgrounds. Earlier, in 1991 Frackowiak showed that the GPert mutation was allelic to the ari-e mutants in barley. The ari-emutants were salt tested and found to show the same positive responses to salt stress as Golden Promise. This supported the
allelism tests, and consequently the GPert symbol was changed to ari-e.GP. The semi-dwarf mutant sdw1 (also known as denso) and the erectoides semi-dwarf mutant,ert-k32 were also tested for their effects on tolerance to salt, but did not show any positive effects. Salt tolerance was therefore
not a general phenomenon of semi-dwarf stature but specific to mutations at the Ari-e locus in these lines. Genetic markers (RAPDs, AFLPs and SSRs) have been used for fingerprinting, genetic mapping, and QTL
analysis. The markers have helped 1) confirm the isogenic relationship between Maythorpe and Golden Promise, 2)clarify the
confusion over the pedigree of Golden Promise, and 3) genetically map the ari-e.GPlocus and examine its pleiotropic effects.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献
Hexaploid triticale (X Triticosecale Wittmack) (2n= 6x= 42, AABBRR) and wheat (Triticum aestivum L.) (2n= 6x= 42, AABBDD) differ in their R and D-genomes. This produces differences in both agronomic and end-use quality characteristics. Our objective was to determine how introgressions of individual chromosomes from the D-genome of wheat affect these characteristics of a winter triticale 'Presto'. We studied the effects of 18 D-genome chromosome substitution lines, 15 sib-lines as controls, and five check cultivars at Lincoln, NE in 1996, using a randomized complete block design with two replications. The experiment was repeated at Lincoln and Mead, NE in 1997 and 1998 with 15 substitution lines that survived the first winter in Lincoln, along with their 12 control sibs and five check cultivars. Few D-genome chromosomes had positive effects. Chromosomes 2D, 4D, and 6D significantly reduced plant height when substituted for 2R, 4B, and 6R, respectively. No grain yield increases were associated with any of the D-genome chromosomes tested, but three substitutions decreased the grain yield. Depending on the allele of the hardness gene present, chromosome 5D increased or decreased kernel hardness when substituted for 5R or 5A, respectively. Introgressions of chromosomes 1D and 6D improved end-use quality characteristics of Presto. These results suggest that apart from beneficial effects of individual loci located on the D-genome chromosomes, no major benefit can be expected from D-genome chromosome substitutions. 相似文献
Douglas fir (Pseudotsuga menziesii (Mirb.) Franco) needle-litter was given treatments of varying biocidal severity including air-drying, oven-drying, fumigation with methyl bromide plus chloropicrin. autoclaving, and a control. The litter was inoculated with a small amount of fresh litter homogenate and monitored for CO2 evolution rate and extractable enzymatic activity during a 77-day incubation. Enzymatic activities assayed included cellulase. xylanase, mannase, amylase. invertase, β-glucosidase, protease, polyphenoloxidase and peroxidase. The concentrations of extractable ninhydrin-reactive compounds, glucose, and reducing substances were also determined.
Air-drying produced a small, initial stimulation in respiration but had no effect on any enzymatic activity throughout the 77-day incubation except for an initial decrease in polyphenoloxidase and peroxidase activities. Oven-drying produced a substantial loss of all enzymatic activities initially but all carbohydrase and protease activities recovered to greater than control levels by 7 days; after a 1-day lag, oven-drying produced a pronounced stimulation in the rate of CO2 evolution. Autoclaving produced a 2-day lag in a less pronounced (compared to oven-drying) respiratory stimulation: initially all enzymatic activities were destroyed and only protease and β-glucosidase activities recovered to control levels. Fumigation produced a respiratory stimulation after a 9-day lag (probably due to residual chloropicrin) which coincided with a pronounced increase in cellulase. xylanase, mannase and amylase activities: initially, no activities except polyphenoloxidase and peroxidase were adversely affected by fumigation.
During the entire incubation, the activities of cellulase. xylanase. mannase. amylase and invertase were highly correlated with each other regardless of treatment. After 77 days, the rates of CO2 evolution of all samples were correlated with the level of amylase and cellulase activity (r = 0.86 and 0.83, respectively). This observation points to the value of enzymatic assays for following the processes which release substrate for microbial assimilation from plant litter. The close association of polysaccharidase and protease activities with the flush of CO2 evolution following biocidal treatment, particularly oven-drying, indicates that the decomposition of carbohydrates and proteins released from microbial biomass or plant litter is a mechanism for this often-observed respiratory stimulation. 相似文献
