Biology subjects

Gaginskaya, E.

Publications and source records attributed to Gaginskaya, E..

3 recordsLinked to original sources

bioRxiv2026

Evidence of two centromeres in the germline-restricted chromosome (GRC): insights from zebra finch lampbrush chromosomes

The germline-restricted chromosome (GRC) of the zebra finch Taeniopygia guttata represents a well-established model of programmed DNA elimination in vertebrates. Although the DNA composition of the GRC, as well as elimination processes during spermatogenesis and early embryogenesis, have been characterised previously, little is known about the cytogenetic features underlying its unusual behaviour, including its stable transmission through the maternal germline. Here, we provide a detailed characterisation of the zebra finch GRC at the diplotene stage of female meiosis, when chromosomes are actively transcribed and acquire the form of giant lampbrushes. We identified a transcriptionally repressed region on the GRC, which we term the belt. Microdissection and sequencing of the belt revealed that it is predominantly composed of a tandem repeat derived from the dph6 gene, robo1 gene fragments, and ERVs. Notably, the terminally located functional centromere of the GRC lacks typical zebra finch centromeric satellites and, conversely, consists of the newly identified GRC-specific tandem repeats Tgut16-201 and Tgut17-167. The canonical centromeric repeat Tgut716 was observed in the GRC belts. Moreover, belts, like the terminal GRC centromere, were associated with coilin-containing nuclear bodies, which serve as markers of centromeric regions on zebra finch lampbrush chromosomes. Together, our findings provide evidence for the presence of one functional and one putative centromeric region on the zebra finch GRC, suggesting their role in non-Mendelian inheritance of the GRC. Author summaryGermline-restricted chromosomes (GRCs) are unusual chromosomes that are retained in germ cells but eliminated from somatic cells during early development. They have evolved independently in several groups of organisms, but are particularly notable in passerine birds, a large monophyletic vertebrate clade ([~]6,700 species) in which GRCs have persisted for at least 44 million years. Passerine GRCs are normally transmitted to the next generation through the maternal germ cell, however, the mechanisms ensuring their inheritance remain unknown. To address this question, we examined the structure of the zebra finch GRC during female meiosis. We found that the GRC differs from all other chromosomes in possessing two distinct centromeric regions: a functional terminal centromere and an extended heterochromatic region exhibiting centromeric properties. These unusual features suggest a mechanism by which the GRC may achieve its preferential transmission through the female germline. Our findings substantially advance the understanding of the zebra finch GRC and the general biology of passerine GRCs. By revealing chromosome features that may underlie their non-Mendelian inheritance, this work provides new insights into the evolution and behaviour of GRCs and other selfish chromosomes that bias their own transmission.

genetics↗

bioRxiv2019

Amyloid conformers of the FXR1 protein prevent mRNA degradation in cortical neurons

Functional amyloids regulate vital processes in a variety of organisms from bacteria to higher eukaryotes. The development of methods enabling large-scale screening for amyloids opens up opportunity for systemic analysis of the prevalence of amyloids in nature. Using an original proteomic approach, we identified several proteins forming amyloid-like detergent-resistant aggregates in the rat brain. One of them is the FXR1 protein, which is known to regulate memory and emotions (1, 2). We demonstrated that in brain FXR1 forms amyloid oligomers and insoluble detergent-resistant aggregates that strongly colocalize with amyloid-specific dye Thioflavin S and bind mRNA molecules. Moreover, we demonstrated that mRNAs colocalized with FXR1 amyloid particles are completely resistant to treatment with RNAse A. Taking into consideration that the members of ribonuclease A superfamily function in neurons (3) we can conclude that amyloid conformers of FXR1 control RNA stability in brain. Thus, in contrast to pathological amyloids that cause neurodegeneration, FXR1 is the functional amyloid in forebrain. We showed that amyloid properties of FXR1 depend on its N-terminal part from 1 to 379 amino acids. This fragment forms amyloid fibrils in vitro that bind Congo red and manifest apple-green birefringence when assayed by polarization microscopy. The amyloid-forming region of FXR1 is highly conserved in mammals. These data suggest that the ability of amyloid conformers of FXR1 to protect mRNAs is characteristic of different mammalian species, including humans. Significance StatementAmyloids are highly ordered cross-{beta} sheet protein fibrils associated with many neurodegenerative diseases including Alzheimers disease. However, some amyloid proteins regulate vital processes. We identified a set of proteins that form amyloid-like aggregates in the brain of healthy rats. One of them - the FXR1 protein is known to regulate memory and emotions. FXR1 forms amyloid fibrils that bind RNA molecules and prevent their degradation in brain cortex neurons. Amyloid-forming sequence of FXR1 is highly conserved across mammals including human. Discovery of functional amyloids in mammalian brain shows that strategy aimed at the development of universal anti-amyloid drugs is unpromising. Such potential drugs should prevent or suppress formation of pathological aggregates of a certain protein, but not affect functional amyloids.

neuroscience↗

bioRxiv2017

Evolution of ribosomal internal transcribed spacers in Deuterostomia

Sequences of ribosomal internal transcribed spacers (ITSs) are of great importance to molecular phylogenetics and DNA barcoding, but remain unstudied in some large taxa of Deuterostomia. We have analyzed complete ITS1 and ITS2 sequences in 62 species from 16 Deuterostomia classes, with ITSs sequences in 24 species from 11 classes initially obtained using unannotated contigs and raw read sequences. A general tendency for both ITS length and GC-content increase from interior to superior Deuterostomia taxa, a uniform GC-content in both ITSs within the same species, thymine content decrease in sense DNA sequences of both ITSs are shown. A possible role of GC-based gene conversion in Deuterostomia ITSs evolutionary changes is hypothesized. The first example of non-LTR retrotransposon insertion into ITS sequence in Deuterostomia is described in turtle Geochelone nigra. The roles of mobile genetic element insertions in the evolution of ITS sequences in some Sauropsida taxa are discussed as well.

molecular biology↗