Influence of certain soil factors on chocolate spot of beans

In the summer of 1941 chocolate spot of beans was widespread in the South-Eastern Agricultural Province and caused much damage to the crop. Soil samples were collected from forty-nine affected fields on a variety of soil types, and the relation between the severity of attack by chocolate spot and the texture, pH, available potassium and available phosphorus determined. Severity of attack was classified into three grades: 'slight', in which only spotting of the foliage occurred; 'moderate', in which death of leaves and blossoms on the three or four lowest nodes occurred; and 'severe', in which there was generally a total loss of crop. No significant relation between severity of attack and soil texture, pH or available potassium was found. A highly significant relation was found to exist between the severity of attack and the amount of available phosphorus in the soil as determined by the method of soil analysis used in this Province. Damage by chocolate spot was generally slight on soils containing 'medium to medium high' or higher amounts of available phosphorus, and generally severe on soils containing low amounts of available phosphorus.     

A technique for hypophysectomy of neonatal rats

A new technique for hypophysectomy of 4 to 6 day old neonatal rats is described. A success rate of 82% was obtained on 6 day old neonates, and they showed a 50% reduction in growth rate. The advantages of this new technique are discussed. It provides a method for directly studying the pituitary contribution to development in the preweaned rat pup.     

Experiments to determine the effect of certain wood preservatives on the growth and cropping of the cultivated mushroom (Psalliota campestris)

A small-scale laboratory method of determining the effect of wood preservatives on growth and cropping of the cultivated mushroom is outlined. Experiments with a number of well-known wood preservatives are described. According to these experiments wood treated with the following preservatives had no adverse effect on mycelial growth or on croppings: 5 % copper sulphate solution, green Cuprinol, 5 % Celcure solution, 2 % Triolith (Wolman salts) solution. On the other hand, wood treated with 2 % Chromel salt and coal-tar creosote reduced the vigour of growth of mushroom mycelium to a depth of 1/2 in. in compost that was in contact with it. Under these conditions, however, the mycelium was not killed nor was the cropping reduced even when the treated wood was only 1 1/2 in in. below the casing soil. As in all experiments the treated wood was covered with compost, the chance of vapours from the preservatives coming into contact with sporophores was very small, and the possibility of harmful effect in mushroom houses from such vapours should not be ignored.
The experiments indicate that full-scale trials in commercial mushroom houses could be undertaken with copper sulphate, green Cuprinol, Celcure and Triolith with negligible risk to the crop, but that it is advisable to carry out trials on a smaller scale with Chromel and coal-tar creosote of known composition to determine whether these preservatives have any adverse effect on cropping. Owing to the great range in composition shown by coal-tar creosote it is most important that the conclusions reached with the particular sample used in the above experiments should not be applied to creosotes in general.     

Drosophila couch potato mutants exhibit complex neurological abnormalities including epilepsy phenotypes

RNA-binding proteins play critical roles in regulation of gene expression, and impairment can have severe phenotypic consequences on nervous system function. We report here the discovery of several complex neurological phenotypes associated with mutations of couch potato (cpo), which encodes a Drosophila RNA-binding protein. We show that mutation of cpo leads to bang-sensitive paralysis, seizure susceptibility, and synaptic transmission defects. A new cpo allele called cpo(EG1) was identified on the basis of a bang-sensitive paralytic mutant phenotype in a sensitized genetic background (sda/+). In heteroallelic combinations with other cpo alleles, cpo(EG1) shows an incompletely penetrant bang-sensitive phenotype with approximately 30% of flies becoming paralyzed. In response to electroconvulsive shock, heteroallelic combinations with cpo(EG1) exhibit seizure thresholds less than half that of wild-type flies. Finally, cpo flies display several neurocircuit abnormalities in the giant fiber (GF) system. The TTM muscles of cpo mutants exhibit long latency responses coupled with decreased following frequency. DLM muscles in cpo mutants show drastic reductions in following frequency despite exhibiting normal latency relationships. The labile sites appear to be the electrochemical GF-TTMn synapse and the chemical PSI-DLMn synapses. These complex neurological phenotypes of cpo mutants support an important role for cpo in regulating proper nervous system function, including seizure susceptibility.     

The mei-P26 gene encodes a RING finger B-box coiled-coil-NHL protein that regulates seizure susceptibility in Drosophilia

Seizure-suppressor mutations provide unique insight into the genes and mechanisms involved in regulating nervous system excitability. Drosophila bang-sensitive (BS) mutants present a useful tool for identifying seizure suppressors since they are a well-characterized epilepsy model. Here we describe the isolation and characterization of a new Drosophila seizure-suppressor mutant that results from disruption of the meiotic gene mei-P26, which belongs to the RBCC-NHL family of proteins. The mei-P26 mutation reduces seizures in easily shocked (eas) and slamdance (sda) epileptic flies following mechanical stimulation and electroconvulsive shock. In addition, mutant mei-P26 flies exhibit seizure thresholds at least threefold greater than those of wild type. The mei-P26 phenotypes appear to result from missense mutation of a critical residue in the NHL protein-protein interaction domain of the protein. These results reveal a surprising role for mei-P26 outside of the germline as a regulator of seizure susceptibility, possibly by affecting synaptic development as a ubiquitin ligase.     

PCR-based microsatellite analysis for differentiation and genetic monitoring of nine inbred SENCAR mouse strains

Sixteen DNA microsatellites or simple sequence length polymorphisms (SSLPs), generated by polymerase chain reaction (PCR) were selected for use in the genetic quality control of the nine inbred SENCAR strains currently available. The SENCAR strains constitute a powerful tool for mechanistic studies of multi-stage skin carcinogenesis, as well as for studies to understand the underlying genetic basis of resistance to tumour promotion and progression. SSLP analysis is a fast and economical way for detecting genetic contamination (unexpected outcrosses) among these closely-related albino strains, where standard immunological and biochemical markers have been shown to be insufficient.     

Whole-genome sequencing and variant discovery in C. elegans

Massively parallel sequencing instruments enable rapid and inexpensive DNA sequence data production. Because these instruments are new, their data require characterization with respect to accuracy and utility. To address this, we sequenced a Caernohabditis elegans N2 Bristol strain isolate using the Solexa Sequence Analyzer, and compared the reads to the reference genome to characterize the data and to evaluate coverage and representation. Massively parallel sequencing facilitates strain-to-reference comparison for genome-wide sequence variant discovery. Owing to the short-read-length sequences produced, we developed a revised approach to determine the regions of the genome to which short reads could be uniquely mapped. We then aligned Solexa reads from C. elegans strain CB4858 to the reference, and screened for single-nucleotide polymorphisms (SNPs) and small indels. This study demonstrates the utility of massively parallel short read sequencing for whole genome resequencing and for accurate discovery of genome-wide polymorphisms.     

Mutational spectrum in the neurofibromatosis type 2 gene in sporadic and familial schwannomas

Using a heteroduplex approach and direct sequencing, we have completed the screening of approximately 88% of the neurofibromatosis type 2 (NF2)-coding sequence of DNA extracted from 33 schwannomas from NF2 patients and from 29 patients with sporadic schwannomas. The extensive screening has resulted in the identification of 33 unique mutations. Similarly to other human genes, we have shown that the CpG sites are more highly mutable in the NF2 gene. The frequency, distribution, and types of mutations were shown to differ between the sporadic and familial tumors. The majority of the mutations resulted in protein truncation and were consistent with more severe phenotype, however three missense mutations were identified during this study and were all associated with milder manifestations of the disease. Received: 25 September 1995 / Revised: 19 December 1995