Sorbitol dehydrogenase in Anas platyrhynchos and Zenaida auriculata auriculata during development.

Sorbitol dehydrogenase (E.C.N. 1.1.1.14) was studied in liver, kidney and gonads of Zenaida auriculata auriculata (golden pigeon) and of Anas platyrhynchos (creole domestic duck) from South American faunes. The specific activity of SDH increased from embryonic to adult stage and is higher in the Anas platyrhynchos tissues. The electrophoretic studies performed in liver and kidney of both species during development showed variations in the number and intensity of the bands in accordance with the age and the species.     

Synapse-like profiles in regenerating sensory nerve fibres of Herbst corpuscles.

During regeneration sequences of Herbst corpuscles, the synapse-like structures are described between pairs of non-myelinated sensory profiles. The probable significance of this unusual for sensory corpuscles finding is discussed.     

Colchicine-estrogen interactions

Summary Colchicine does not block estrogen-induced recognition of uterine blood vessel surface by eosinophils, but interfers with their migration through endothelial lining and therefore blocks estrogen-induced uterine eosinophilia and edema.Acknowledgments. This work was supported by grant 4002 from the Servicio de Desarrollo Científico y Creación Artística of the University of Chile. Technical help of Mr D. Sáez is appreciated.     

Uncoupling of the recombination and topoisomerase activities of the gamma delta resolvase by a mutation at the crossover point

In several well-characterized site-specific recombination systems it has been shown that, for efficient recombination, the two recombining sites must have identical DNA sequences across the region between the staggered points of exchange. The precise DNA sequence of this overlap region, however, appears to be of little importance (with the exception of one position in the loxP site of bacteriophage P1 (ref. 6]. In this report we characterize a mutant recombination site for the site-specific recombination enzyme gamma delta resolvase (encoded by the gamma delta transposon), in which the dinucleotide at the crossover point is changed from AT to CT. Our results indicate that identity of the two overlap regions is not sufficient for recombination. Although resolvase binds normally to the mutant site and induces the structural deformation characteristic of the wild-type recombination site, catalysis at the crossover point (cutting and rejoining of DNA strands) is effectively limited to just one of the two strands, allowing resolvase to act as a topoisomerase but not as a recombinational enzyme.