106 results match your criteria: "Center for Molecular and Cellular Biology[Affiliation]"

Using BW25113 as a host, we isolated a novel lytic phage from the commercial poly-specific therapeutic phage cocktail Sextaphage (Microgen, Russia). We provide genetic and phenotypic characterization of the phage and describe its host range on the ECOR collection of reference strains. The phage, hereafter named Sxt1, is a close relative of classical coliphage T3 and belongs to the genus, yet its internal virion proteins, forming an ejectosome, differ from those of T3.

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In our large-scale search for antimicrobial-producing bacteria, we isolated an actinomycete strain from rhizospheric soil of . The strain designated BP-8 showed noticeable antibacterial activity. BP-8 was subjected to a whole-genome analysis via a polyphasic taxonomy approach, and its antibacterial metabolite was identified by HRLS-MS.

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Antibiotic resistance has been and remains a major problem in our society. The main solution to this problem is to search and study the mechanisms of antibiotic action. Many groups of secondary metabolites, including antimicrobial ones, are produced by the phylum.

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Aminoglycosides are one of the first classes of natural antibiotics which have not lost relevance due to their broad spectrum of action against Gram-positive, Gram-negative bacteria and mycobacteria. The high growth rate of antimicrobial resistance (AMR) together with the severe side effects of aminoglycosides increase the importance of developing improved semisynthetic derivatives. In this work, we proposed a synthetic route to new tobramycin derivatives modified at the 6″-position with aminoalkylamine or guanidinoalkylamine residues.

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Puromycin (Puro) is a natural aminonucleoside antibiotic that inhibits protein synthesis by its incorporation into elongating peptide chains. The unique mechanism of Puro finds diverse applications in molecular biology, including the selection of genetically engineered cell lines, in situ protein synthesis monitoring, and studying ribosome functions. However, the key step of Puro biosynthesis remains enigmatic.

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Eukaryotic cells express a large number of transcripts from a single gene due to alternative splicing. Despite hundreds of thousands of splice isoforms being annotated in databases, it has been reported that the current exon catalogs remain incomplete. At the same time, introns of human protein-coding (PC) genes contain a large number of evolutionarily conserved elements with unknown function.

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RE-1 silencing transcription factor (REST) is a key repressor of neural genes. REST is upregulated under stress signals, aging and neurodegenerative diseases, but although it is upregulated, its function is lost in Alzheimer's Disease. However, why it becomes inactive remains unclear.

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Article Synopsis
  • Argonaute proteins are versatile nucleases present in all life forms, with eukaryotic versions involved in gene regulation and defense against viruses, while their prokaryotic counterparts help bacteria fend off invading genetic material.
  • Recent research indicates that prokaryotic argonautes (pAgos) may protect bacteria from the antibiotic ciprofloxacin, suggesting a potential role in DNA replication and repair.
  • The authors propose models for how pAgos could contribute to ciprofloxacin resistance, including assisting with DNA decatenation, processing DNA repair intermediates, or triggering the SOS response that enhances overall DNA repair and antibiotic resistance.
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Enzymatic tools for mitochondrial genome manipulation.

Biochimie

October 2024

Center for Molecular and Cellular Biology, Skolkovo Institute of Science and Technology, Moscow, 143026, Russian Federation; Department of Biology and Genetics, Petrovsky Medical University, Moscow, 117418, Russian Federation. Electronic address:

Mutations in mitochondrial DNA (mtDNA) can manifest phenotypically as a wide range of neuromuscular and neurodegenerative pathologies that are currently only managed symptomatically without addressing the root cause. A promising approach is the development of molecular tools aimed at mtDNA cutting or editing. Unlike nuclear DNA, a cell can have hundreds or even thousands of mitochondrial genomes, and mutations can be present either in all of them or only in a subset.

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Telomeres-special DNA-protein structures at the ends of linear eukaryotic chromosomes-define the proliferation potential of cells. Extremely short telomeres promote a DNA damage response and cell death to eliminate cells that may have accumulated mutations after multiple divisions. However, telomere elongation is associated with the increased proliferative potential of specific cell types, such as stem and germ cells.

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Modified (2'-deoxy)adenosines activate autophagy primarily through AMPK/ULK1-dependent pathway.

Bioorg Med Chem Lett

November 2024

Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Russian Academy of Sciences, 117997 Moscow, Russia; RUDN University, 117198 Moscow, Russia. Electronic address:

Article Synopsis
  • * Scientists think that by activating autophagy, we can help treat diseases like cancer, obesity, and neurodegenerative diseases.
  • * A study tested some new compounds to see if they could activate autophagy better than a common drug called AICAr, and found some that worked well even without needing a specific protein called AMPK.
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Genetically encoded epigenetic sensors for visualization of H3K9me3, H3K9ac and H3K4me1 histone modifications in living cells.

Biochem Biophys Res Commun

November 2024

Center for Molecular and Cellular Biology, Skolkovo Institute of Science and Technology, Bolshoi Blvd. 30, Bld. 1, 121205, Moscow, Russia; Shemyakin-Ovchinnikov Institute of Bioorganic Chemistry, Miklukho-Maklaya 16/10, 117997, Moscow, Russia; Pirogov Russian National Research Medical University, Ostrovityanova 1, 117997, Moscow, Russia. Electronic address:

Post-translational modifications of histones play a crucial role in chromatin structure maintenance and epigenetic regulation. The LiveMIEL (Live-cell Microscopic Imaging of Epigenetic Landscape) method represents a promising approach for tracking histone modifications. It involves visualization of epigenetic modifications using genetically encoded fluorescent sensors and further analysis of the obtained intranuclear patterns by multiparametric image analysis.

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Article Synopsis
  • Expansion of CAG repeats in certain genes is linked to neurodegenerative diseases, but the mechanisms are not well understood; this study investigates how these repeats interact with RNA editing enzymes like ADAR.
  • Researchers used induced pluripotent stem cells (iPSCs) and brain organoids from Huntington's disease and ataxia type 17 patients to analyze RNA editing via next-generation sequencing.
  • Results showed that while some brain organoids with specific CAG repeats had decreased RNA editing, most cultures did not support the hypothesis that CAG repeats affect editing levels significantly.
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Viruses compete with each other for limited cellular resources, and some deliver defence mechanisms that protect the host from competing genetic parasites. The phage antirestriction induced system (PARIS) is a defence system, often encoded in viral genomes, that is composed of a 55 kDa ABC ATPase (AriA) and a 35 kDa TOPRIM nuclease (AriB). However, the mechanism by which AriA and AriB function in phage defence is unknown.

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Article Synopsis
  • Plasmid-borne Type II restriction-modification (RM) systems cause post-segregational killing (PSK) due to the loss of restriction and modification enzymes during cell division, leading to the breakdown of unmethylated DNA.
  • A CRISPR interference method was developed to investigate PSK and found that different RM systems have distinct stability and recovery behaviors upon plasmid loss, particularly noting the Esp1396I system's limited duration of activity.
  • This research suggests that the dynamics of RM systems and host cell growth rates are crucial for understanding PSK, highlighting the need to consider the lifetimes of system components in modeling these processes.
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  • - Elys/Mel-28 is a nucleoporin (Nup) that connects decondensing chromatin with nuclear pore complexes (NPCs) after mitosis, but its role during interphase is unclear.
  • - Research using DamID-seq in Drosophila embryos identified different Elys binding sites within active or inactive chromatin, revealing its interaction with nucleoplasmic and NPC-linked forms.
  • - Knocking down Elys in S2 cells causes chromatin to move away from the nuclear envelope, leading to gene derepression, while also compacting active chromatin regions, suggesting Elys helps anchor peripheral chromatin to the nuclear envelope.
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The orchid genus comprises three species, all discovered in the 21 century. Each of these species is achlorophyllous, mycoheterotrophic and is known to be endemic to Vietnam. The type species of the genus, , occurs in a single location in northern Vietnam within a lowland limestone karstic area.

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Amino acid preferences at a protein site depend on the role of this site in protein function and structure as well as on external constraints. All these factors can change in the course of evolution, making amino acid propensities of a site time-dependent. When viral subtypes divergently evolve in different host subpopulations, such changes may depend on genetic, medical, and sociocultural differences between these subpopulations.

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From compartments to loops: understanding the unique chromatin organization in neuronal cells.

Epigenetics Chromatin

May 2024

Center for Molecular and Cellular Biology, Skolkovo Institute of Science and Technology, Bolshoy Boulevard 30, Build.1, Moscow, 121205, Russia.

The three-dimensional organization of the genome plays a central role in the regulation of cellular functions, particularly in the human brain. This review explores the intricacies of chromatin organization, highlighting the distinct structural patterns observed between neuronal and non-neuronal brain cells. We integrate findings from recent studies to elucidate the characteristics of various levels of chromatin organization, from differential compartmentalization and topologically associating domains (TADs) to chromatin loop formation.

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Type VI CRISPR-Cas systems are among the few CRISPR varieties that target exclusively RNA. The CRISPR RNA-guided, sequence-specific binding of target RNAs, such as phage transcripts, activates the type VI effector, Cas13. Once activated, Cas13 causes collateral RNA cleavage, which induces bacterial cell dormancy, thus protecting the host population from the phage spread.

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The Siberian frog Rana amurensis has a uniquely high tolerance to hypoxia among amphibians, as it is able to withstand several months underwater with almost no oxygen (0.2 mg/liter) vs. several days for other studied species.

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Article Synopsis
  • Chromatin structure plays a crucial role in determining gene expression and cell identity, especially in neurons, through the action of polycomb group (PcG) proteins.
  • A study mapping the 3D genome in neuronal and non-neuronal cells from the Wernicke's area shows that neurons have less separation between active and inactive gene regions compared to other brain cells.
  • Neuronal cells display unique chromatin interactions, including a specific network of PcG contacts linked to genes that control development, with a distinct pattern of histone modifications that suggest a functional significance of these interactions for neuron identity.
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Posttranslational modifications in fibrinogen resulting from induced oxidation or oxidative stress in the organism can have deleterious influence on optimal functioning of fibrinogen, causing a disturbance in assembly and properties of fibrin. The protective mechanism supporting the ability of fibrinogen to function in ROS-generating environment remains completely unexplored. The effects of very low and moderately low HOCl/OCl concentrations on fibrinogen oxidative modifications, the fibrin network structure as well as the kinetics of both fibrinogen-to-fibrin conversion and fibrin hydrolysis have been explored in the current study.

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The study of urinary peptidome is an important area of research, which concerns the characterization of endogenous peptides, as well as the identification of biomarkers for a wide range of socially significant diseases. First of all, this relates to renal and genitourinary pathologies and/or pathologies associated with proteinuria, such as kidney diseases, bladder, prostate and ovarian cancers, diabetic nephropathy, and pre-eclampsia. Unlike proteins, peptides do not require proteolytic hydrolysis, can be analyzed in their native form and can provide certain information about occurring (patho)physiological processes.

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