Log-linear models for linked loci

A clarification is given of the difference between a multiplicative model (Haber, 1984, Biometrics 40, 189-198) and an additive model (Weir, 1979, Biometrics 35, 235-254) for association between genes at two loci. Although the parametrization of Haber contains both intergametic and intragametic linkage disequilibrium terms, there are problems in separating these terms when the two types of double heterozygote cannot be distinguished. An alternative formulation that contains the sum and product of these terms also contains measures of association between three or four genes at two loci, and a reexamination of data discussed by Haber shows that the inclusion of trigenic disequilibria can significantly improve the fit of the model.     

A comparison of the nodulation of diploid and tetraploid varieties of red clover inoculated with different Rhizobial strains

Summary The effectiveness of three different strains ofRhizobium trifolii on a diploid and a tetraploid variety of red clover (Trifolium pratense) grown in aseptic mineral-agar culture was compared. It was found that with two of the rhizobial strains tested, the tetraploid plants were slower to nodulate than the diploid plants, but that a hundred per cent nodulation was obtained in both cases. With the third strain, however, a sixty-six per cent nodulation of the diploid plants was reduced to an eight per cent nodulation of the tetraploids.In general, over a given period, fewer nodules were formed on the tetraploid plants, but these tended to be larger than on the diploids. The fresh weight of the tetraploid plants always exceeded that of the diploids, but less so in cases of poorly nodulated plants.     

Hemoglobin causes release of inositol trisphosphate from vascular smooth muscle

To test the hypothesis that oxyhemoglobin causes contraction of vascular smooth muscle by production of inositol 1,4,5-trisphosphate which results in a release of intracellular calcium, smooth muscle cells were exposed to oxyhemoglobin and inositol trisphosphate was measured. Oxyhemoglobin, but not methemoglobin which has much less contractile action, stimulated inositol trisphosphate production. The time course was consistent with an early role for this compound in the contraction produced by hemoglobin. The increase in production of inositol trisphosphate was inhibited by pertussis toxin and also by neomycin, an inhibitor of phospholipase C, although the actions of the latter compound cannot be attributed only to an inhibition of the enzyme responsible for the production of inositol trisphosphate.     

The design of potent, selective, non-covalent, peptide thrombin inhibitors utilizing imidazole as a S1 binding element.

Modeling of neutral or mildly basic functional groups in the S1 site of thrombin led to the targeting of imidazole as a S1 binding element and correctly predicted the optimal chain length for connecting this group with the S2 and S3 binding elements. Derivatives of 4-(3-aminopropyl)-imidazole can be selective inhibitors of thrombin demonstrating potent anticoagulant activity.