Biomedical subjects

A Bayev

Publications and source records attributed to A Bayev.

5 recordsLinked to original sources

PubMed1990

The 5'-flanking sequence of the loach oocyte 5S rRNA gene contains a signal for effective transcription.

Deletion mutants of loach oocyte 5S rRNA genes were injected and transcribed in vivo in the nuclei of loach (Misgurnus fossilis) and Xenopus laevis. A control region was found in the 5'-flanking sequence, the elimination of which greatly decreases in vivo transcription of 5S rRNA genes. This cis-acting element is located in the region between nt-18 and the transcription start point. We propose that the oocyte nucleus contains (a) specific transcriptional factor(s), NTFO, which interacts with the cis-acting element we described. We also propose that NTFO is inactivated in maturing oocytes when nucleoplasm interacts with oocyte cytoplasm after germinal vesicle breakdown. The residual activity of this factor(s) may be responsible for low-level synthesis of oocyte 5S rRNA at the beginning of embryogenesis. We consider the disappearance of NTFO during gastrulation to be responsible for the total inactivation of oocyte 5S rRNA genes in embryonic and somatic tissue.

Animals↗

PubMed1982

Organization of loach ribosomal genes (Misgurnus fossilis L.).

The organization of ribosomal genes in the genome and amplified nucleoli of loach (Misgurnus fossilis L.), a teleost fish, was studied. Ribosomal DNA (rDNA) was isolated by density gradient centrifugation, digested by EcoRI endonuclease and mapped with 18S and 28S rRNAs. The transcription unit of ribosomal genes in oocyte nucleoli was investigated by an electron-microscopic visualization technique. The repeat unit of loach rDNA was shown to be split by EcoRI into two fragments: a constant fragment (3 . 10(6) daltons) and heterogeneous one (11-13 . 10(6) daltons, major type, and 7-8 . 10(6) daltons, minor type). The average size of the transcription units was found to be 2.5 +/- 0.2 microm. The lengths of nontranscribed spacers varied from 2.4 to 2.9 microm; however, shorter ones of 1.2-1.4 microm were also noticed. The data indicate that loach rDNA is organized as tandem repeat units of two types: a major fraction of 20-25 kb (14-17 . 10(6) daltons) and a minor one 15-16 kb (10-11 . 10(6) daltons). The heterogeneous length of the repeat units was predetermined by the heterogeneity of nontranscribed spacers.

Animals↗

PubMed1981

The structure of the yeast ribosomal RNA genes. 3. Precise mapping of the 18 S and 25 S rRNA genes and structure of the adjacent regions.

The 5'-terminal of Saccharomyces cerevisiae 18 S and 25 S rRNA are precisely mapped within the sequence of the rDNA repeating unit. The 3'-terminal of 25 S rRNA and 37 S pre-rRNA are located within a 548 bp segment of the rDNA repeating unit by the use of a DNA polymerase I extension technique. The analysis of the rDNA sequences at the structural gene boundaries reveals the presence of oligonucleotide repeats which may be involved in transcription or processing control mechanisms. The sequence of rDNA in the transcription termination region is determined and possible mechanisms shaping the 3'-end of 25 S rRNA are discussed.

Base Sequence↗

PubMed1980

Complementation of T4 phage am mutations by hybrid phages lambda-T4.

EcoRI fragments of the T4 cytosine-containing DNA (dC-DNA) were cloned in the lambda XIII vector phage carrying the only restriction site for EcoRI in the repressor gene of lambda. 38 genes of T4 were identified in the cloned fragments by means of marker rescue technique. All cloned early genes and some late genes of T4 were able to complement a corresponding am mutations of T4 phage when nonpermissive cells of E.coli were simultaneously infected with hybrid phages lambda-T4 and am mutants of T4. An average burst size for am mutants from su- cells (when complemented by corresponding hybrid phage) was 20-70 pfu for early genes and 1-3 to 20 pfu for late ones. When the extract of cells infected with hybrid phage lambda-T4-22 containing T4 genes 57, 1, 2, 64 was mixed with the extract of cells infected with T4N51 mutant, the complementation in vitro was observed. So, it was shown that normal product of late gene 2 is synthesized in the cells infected with hybrid phage lambda-T4-22 in the absence of positive regulators of transcription coded by early T4 genes.

Bacteriophage lambda↗

PubMed1980

Functional analysis of hybrid plasmids carrying genes for lambda site-specific recombination.

A number of hybrid plasmids, carrying lambda genes involved in site-specific integrative recombination, have been constructed in vitro. Analysis of protein synthesis in Escherichia coli minicells has shown that Int protein is synthesized only when int gene is expressed constitutively. The plasmids RSF2124::lambda-CD, RSF2124::lambda-Cint-c57, and pInt lambda were able to integrate into the chromosome of E.coli at the attB. The integration of hybrid plasmids into the genome of bacteria has also been shown for polA1 strains restricting the autonomous replication of ColE1 type plasmids. Genetic markers of hybrid plasmids are maintained in polA1 bacteria for at least 50 generations under nonselective conditions. The Southern blotting experiments using [32P]pBR322 DNA and EcoRI fragments of E. coli polA1 chromosome carrying integrated plasmid pInt lambda demonstrated that in this strain hybrid plasmids can be observed only when integrated into the attB of the chromosome according to Campbell's model of integration. In the cells, where autonomous replication of plasmids is possible, they can be observed both in extrachromosomal and integrated states. The integration of the ColE1 replication origin into the chromosome of bacteria is not lethal for the cells. Only attP and the int gene of lambda are necessary for the integration of hybrid plasmids under conditions of effective int gene expression. If the level of Int protein synthesis is high enough, the prophage excision can be observed in the absence of Xis product. The six-fold decrease of Int protein concentration in the cell (in case of pInt lambda 2 as compared to pInt lambda 1) is critical both for integration and excision.

Bacteriophage lambda↗