Genome Editing As an Approach to the Study of in Vivo Transcription Reprogramming.

CDK8-mediated transcriptional reprogramming is essential for an extensive gene expression. Constitutive knockouts of the cdk8 gene are lethal at the morula stage. For modeling transcriptional reprogramming in an adult organism, we investigated the possibility to attenuate the CDK8 kinase activity with a F97G mutation in exon 3 of the cdk8 gene. According to preliminary experimental data, this mutation should lead to a decrease in CDK8 kinase activity. To edit the genome of laboratory mice, the CRISPR/Cas9 technology was used, in which the introduction of a double-stranded gap occurred at a distance of 128 nucleotide pairs from the planned site of the introduced mutation. To introduce the mutation, a matrix for homologous repair was used as part of plasmid DNA, with homologous arms 903 and 484 bp in the 5'-3' region from the point of double-stranded rupture, respectively. As a result, mice with site-specific target mutations in exon 3 of the cdk8 gene were obtained. We for the first time demonstrated a high efficacy of the mutation 128 bp apart from the site of double-strand break. Viable animals with the F97G mutation in the catalytic domain of CDK8 kinase were obtained for the first time. The resulting cdk8 mutant mice will be used in subsequent studies to simulate the processes involving transcription reprogramming.

Development of a Multiplex PCR Test System for the Determination of a Transgene Based on the pBC1 Plasmid and Its Derivatives for the Expression of Recombinant Proteins in Mus musculus Milk.

A multiplex PCR test system for identification of the regulatory sequences of genetic constructs for transformation (promotor, insulator, and terminator) in the Mus musculus genome and for transgenic animal selection by genotyping with horizontal agarose gel electrophoresis detection was developed. The proposed system was validated by genotyping mouse strains producing human lactoferrin, heat shock protein HSP 70, firefly luciferase, and lysozyme, which were obtained by microinjections of linearized DNA into murine zygote pronucleus with random transgene integration into the genome using the pBC1 plasmid for expression of the gene of interest in milk of transformed animals (milk expression vector kit).

[Differential diagnosis of severe forms of cerebral infarct (clinico-echoencephalographic and pathomorphologic study)]. / O differentsial'noi diagnostike tiazhelykh form infarkta mozga (kliniko-ékhoéntsefalograficheskoe i patomorfologicheskoe issledovanie).

Clinical, echoelectroencephalographic and pathomorphological study in 73 patients with grave ischemic insult in arteria cerebralis media region was performed. Brain infarctions caused by thrombosis were characterized by small M-echo displacement 12 hours after process beginning followed by displacement increase in 3-4 days. Brain infarctions caused by thromboembolic process were characterized by small M-echo displacement 6 hours after accident with subsequent fast increase of displacement till mean or great values in the second half of the first day. Supratentorial brain infarctions not connected with thrombosis were not accompanied by M-echo displacement.