A DNA insertion in the apolipoprotein A-I gene of patients with premature atherosclerosis

Apolipoprotein A-I (apo A-I) is the major protein constituent of high-density lipoprotein (HDL). The study of the apo A-I gene is of interest because plasma levels of HDL have been inversely correlated with the development of coronary artery disease and because polymorphisms related to this gene have been associated with hypertriglyceridaemia and premature atherosclerosis. We have recently isolated and characterized the human apo A-I gene and have shown that apo A-I and apolipoprotein C-III (apo C-III) genes are physically linked and that a polymorphism (of unknown frequency in the general population) of the apo A-I gene is inherited as a mendelian trait linked to premature atherosclerosis in an affected family (not the same polymorphism as has previously been reported to be associated with hypertriglyceridaemia). Here we report that this polymorphism is due an at least 6.5-kilobase (kb) DNA insertion in the coding region of the apo A-I gene and that there is no detectable alteration (as determined by limited genomic blotting analysis) of the apo C-III gene of these patients.     

Characterization and antithrombotic action of tissue plasminogen activator

Summary An extractive fibrinolytic enzyme has been characterized and found to belong to the class of vascular plasminogen activators. The agent has been found to have an antithrombotic action in the rabbit.Provided by Dr L. Dussourd d'Hinterland, Laboratoires Pierre Fabre, Castres, France. 1000 units have a fibrinolytic activity of about 15 PU urokinase.     

Aktivität einiger Transaminasen in den mit SO2 behandelten Erbsen-Keimpflanzen

Summary Fifteen-day-old green pea seedlings were intoxicated 48 h by 1% gaseous sulphur dioxide and in their individual organs the activity of glutamate-oxalacetate (l-aspartate: 2-ketoglutarate-aminotransferase) and aspartate-pyruvate (l-alanine: oxalacetate-aminotransferase) transaminases estimated. The activity of glutamate-oxalacetate transaminase in the intoxicated seedlings was lowered in shoots by 77.8% and in roots by 78,9% as compared with the control plants. The activity of aspartate-pyruvate transaminase was lowered in shoots by 33.5%, in roots by 76% and in cotyledons by 54.5% in comparison with the control plants.