Abstract
In husk tomato, Physalis ixocarpa Brot., a wide range of self-incompatibility phenotypes was observed upon self-pollination. Self-incompatibility seems to be a polygenic trait of low heritability, affected by inbreeding depression and by environment. Organ coloration and leaf serration also were found to be polygenic traits. The chromosomes of this species are characterized by conspicuous heterochromatic knobs which would facilitate identification of each pair. Attempts to hybridize P. ixocarpa with P. floridiana L. and P. peruviana L. were unsuccessful. Propagation by cuttings is readily attainable in P. ixocarpa and might be useful for growing and intercrossing field selections in isolation plots.
Abstract
F2 and backcross segregation for heat tolerant × heat sensitive crosses in Chinese cabbage (Brassica campestris L. Group Pekinensis) indicated that heat tolerance was controlled by a single recessive gene.
Resistance to mites and small insects in geranium results from the production of a viscous exudate on tall glandular trichomes present on the plant surface. This exudate exhibits sticky-trap properties immobilizing pests and reducing feeding and fecundity. The exudate is composed of long-chain 6-alkyl salicylic acids known as anacardic acids. The exudate of resistant plants contains 86% unsaturated anacardic acids. Susceptible genotypes possess fewer tall glandular trichomes and a trichome exudate which is dry and ineffective in trapping pests. The exudate from susceptible plants contains 70% saturated anacardic acids, thus explaining the physical state of the exudate. A single dominant locus controls the production of predominantly unsaturated versus saturated anacardic acids and thus resistance versus susceptibility. Other loci condition the ratio of C22:C24 unsaturated anacardic acids and the density of tall glandular trichomes. Current research involves the elucidation of the enzymatic pathway(s) involved in anacardic acid biosynthesis, identification of the regulatory enzymes and isolation of the mRNA transcripts associated with pertinent genes.
In a study of chilling requirement in Malus, broad-sense heritability estimates for the length of vegetative bud dormancy in 43 clones growing under simulated subtropical winter conditions were 0.76 ± 0.04 in 1986 and 0.81 ± 0.04 in 1987. Narrow-sense heritability estimates were 0.66 ± 0.13 in 1986 and 0.69 ± 0.13 in 1987. Seedlings with low chilling requirements (CR) were not observed in crosses where both parents had high bud-chilling requirements. `Koningszuur' did not transmit its long CR to its seedlings. Open-pollinated (OP) seedling populations from the Malus × domestics Borkh. cultivars Anna, Dorsett Golden, Ein Shemer, Khashabi, Winter Banana, and Zabaoani, and the species and interspecific hybrids M. baccata L. DE#98, M. brevipes Rehd., M. ×robusta (Carr.) Rehd. DE#485, M. × robusta No. 5 (`R5'), M. rockii, M. turesi Rehd. PI 34143, and `Rosedale' had at least 5% of their descendants in the lower CR classes. In all but one instance, 50% or more of `Anna' descendants had low CR. Many of these seedlings were within a few classes of the extreme low CR. It is postulated that the low-CR character present in `Anna' is controlled by at least one major dominant gene and that minor genes interact to modulate its effects. Very low-CR cultivars have a shallow bud dormancy. This highly heritable component for low bud CR is related to a failure to develop a deep dormancy state, rather than to acceleration of the termination of the dormancy process.
Abstract
The polymorphism in nine enzyme systems in apple (Malus domestica Borkh.) was analyzed using horizontal starch gel electrophoresis. The systems studied included aspartate aminotransferase, diaphorase, glucosephosphate isomerase, isocitrate dehydrogenase, phosphoglucomutase, and triosephosphate isomerase. The products of at least 27 loci could be distinguished in these systems, 19 of which displayed polymorphism. Joint segregation analysis in populations derived from crosses between highly heterozygous cultivars revealed four multilocus linkage groups: Aat-c–Idh-1, Dia-2–Mdh-4, Gpi-c2-Aat–p, and (Dia-5, Pgm-p1)–(Mdh-2, Tpi-c2). Although several of the populations investigated had been prescreened for resistance to apple scab, cedar-apple rust, or fire blight, no correlation could be established between the inheritance of an allozyme and a resistant phenotype. The high frequency of duplicate loci encountered is in accordance with the postulated tetraploid nature of the genome.
Genetically characterized isozyme loci are useful for taxonomic studies. In an initial study a few Ananas genotypes were used to determine which enzyme systems would give well-resolved banding patterns on starch gels. The enzyme-staining systems that resulted in well-resolved banding patterns were used to survey more Ananas genotypes to identify and characterize isozyme polymorphism. Genetic studies were performed using seedling populations to determine the basis of variability observed among genotypes. Two peroxidase loci and three phosphoglucomutase loci were identified and characterized. Information from these studies, was used to formulate a system by which species and plant introductions could be identified and distinguished.
Abstract
In growth chambers at 26°±2°C (day) and 21°±2° (night), a 15 hour photoperiod delayed flowering on ‘Great Northern (GN) Nebraska #1 sel. 27’ by 47 days and in Plant Introduction (PI) 207262 by 48 days over a 10 hour photoperiod. The cultivars ‘GN 1140’ and ‘GN Nebraska #1’ and a near-isogenic determinate ‘GN Nebraska #1’ flowered at the same time under both photoperiods. Both near-isogenic lines, determinate and the early flowering ‘GN Nebraska #1 sel. 27’ flowered earlier than ‘GN Nebraska #1 sel. 27’ in all field experiments. The near-isogenic determinate ‘GN Nebraska #1’ flowered earlier than the ‘GN Nebraska #1 cultivar in 2 out of 3 field experiments. The delay in flowering of ‘GN Nebraska #1 sel. 27’ was much greater at higher night temperatures at Lincoln than under lower temperatures at Scottsbluff when the photoperiod was the same. Delayed flowering of PI 207262 under long photoperiod was controlled by a single recessive gene.
Early blight (EB), caused by the fungus Alternaria solani, is a destructive disease of tomato (Lycopersicon esculentum) worldwide. Sources of genetic resistance have been identified within related wild species, including green-fruited L. hirsutum and red-fruited L. pimpinellifolium. We have employed traditional protocols of plant breeding and contemporary molecular markers technology to discern the genetic basis of EB resistance and develop tomatoes with improved resistance. Backcross breeding has resulted in the development of germplasm with improved resistance; however, linkage drag has been a major obstacle when using L. hirsutum as a donor parent. To identify and map QTLs for EB resistance, we used several filial and backcross populations derived from interspecific crosses between L. esculentum and either L. hirsutum or L. pimpinellifolium. In each population, an average of seven resistance QTLs were detected. While similar QTLs were detected in different generations of the same cross, generally different QTLs were identified in populations derived from different crosses. The results suggested stability of QTLs across environments and generations but variation in QTLs in different interspecific populations. It is expected that marker-assisted pyramiding of QTLs from different sources results in development of germplasm with strong and durable resistance. Further inspection of the results led to the identification and selection of six QTLs with stable and independent effects for use in marker–assisted selection (MAS). However, to facilitate “clean” transfer and pyramiding of these QTLs, near-isogenic lines (NILs) containing individual QTLs in a L. esculentum background should be developed.
Differences in structural gene expression are responsible for a wide range of responses from human cancer to patterned flowers. Gene silencing is one of the ways in which gene expression is controlled. We have developed a model system to study gene silencing using a gene silencing mutation in Petunia ×hybrida (Star mutation) and the ability of certain viruses to reverse the silencing mutation. This model system was used to characterize how the Star flower color pattern was controlled.
Abstract
A program is described which stores, lists, searches, corrects, appends, and duplicates pedigree records.