Lysine Suppressor in Escherichia coli

Head amber mutant of phage T4D was used to determine the efficiency of suppression and the amino acid inserted by Escherichia coli CA273 (sup-273 formerly Su(+) (beta)). The level of suppression determined was 8%, and the amino acid inserted was shown to be lysine.     

Analysis of EEG Structural Synchrony in Adolescents with Schizophrenic Disorders

A total of 39 healthy adolescents and 45 adolescents with schizophrenic disorders (mean age 12.3 years) were examined to study the EEG structural synchrony as reflecting temporal synchronization of the operational activity of neuronal networks. A significant decrease in the EEG structural synchrony was observed in the adolescents with schizophrenic disorders as compared to the healthy adolescents. The decrease was detected predominantly in the interhemispheric pairs of EEG derivations, as well as in the pairs related to the frontal, temporal (predominantly on the left), and right parietocentral regions. The findings provide evidence in favor of Friston’s hypothesis of disintegration of cortical electrical activity in schizophrenia and extend the hypothesis in that it is the operational synchrony of cortical activity that might suffer first in schizophrenia.__________Translated from Fiziologiya Cheloveka, Vol. 31, No. 3, 2005, pp. 16–23.Original Russian Text Copyright © 2005 by Borisov, Kaplan, Gorbachevskaya, Kozlova.     

Internal EcoRI-generated deletion in prophage Mu DNA

The hybrid plasmid consisting of the plasmid pRP1.2 (derivative of RP4) genome and deleted prophage Mucts 62 genome which lost the central EcoRI fragment of DNA was constructed. The ability of deleted Mu phage to carry out E. coli chromosomal genes transposition was still retained.     

A statistical test for detecting geographic subdivision.

A statistical test for detecting genetic differentiation of subpopulations is described that uses molecular variation in samples of DNA sequences from two or more localities. The statistical significance of the test is determined with Monte Carlo simulations. The power of the test to detect genetic differentiation in a selectively neutral Wright-Fisher island model depends on both sample size and the rates of migration, mutation, and recombination. It is found that the power of the test is substantial with samples of size 50, when 4Nm less than 10, where N is the subpopulation size and m is the fraction of migrants in each subpopulation each generation. More powerful tests are obtained with genes with recombination than with genes without recombination.     

The first seven amino acids encoded by the v-src oncogene act as a myristylation signal: lysine 7 is a critical determinant.

The transforming protein of Rous sarcoma virus, pp60v-src, is covalently coupled to myristic acid by an amide linkage to glycine 2. Myristylation promotes the association of pp60v-src with cellular membranes, and this subcellular location is essential for transforming activity. The findings presented here, in conjunction with the previous reports of others, imply that the seventh amino acid encoded by v-src might be important in the myristylation reaction. Replacement of lysine 7 by asparagine greatly reduced the myristylation, membrane association, and transforming activity of pp60v-src. In contrast, substitution of arginine at residue 7 had no effect on any of these properties of pp60v-src. Addition of amino acids 1 to 7 encoded by v-src was sufficient to cause myristylation of a src-pyruvate kinase fusion protein. We conclude that the recognition sequence for myristylation of pp60v-src comprises amino acids 1 to 7 and that lysine 7 is a critical component of this sequence.