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Biology subjects

Dountcheva, V.

Publications and source records attributed to Dountcheva, V..

3 recordsLinked to original sources

Directionality bias in T/A cloning

T/A cloning is a popular method for generating recombinant DNA plasmids. This method relies on single A:T nucleotide base pairs between PCR product ends and vector. Theoretically, the directionality of insert ligation with relation to the vector is random. However, we have continuously observed directionality bias using the pGEM-T Vector System for T/A cloning in a Course-based Undergraduate Research Experience (CURE). Cloning of over 400 inserts has shown directional bias higher than 74% (p-value < 0.0005) "sense" to the T7 promoter of the vector. Awareness of biased insertion in our applications reduces time and cost in cloning and downstream analyses.

molecular biology↗

Acridine Orange dye for long-term staining and live imaging of cnidarian development and regeneration

As the sister phylum to Bilateria, Cnidaria, holds a phylogenetic position that is crucial in evolutionary studies of animal development. However, the analysis of cnidarian species, as well as other emerging models, is limited by the scarcity of tools that are readily available and applied with ease. Commercial fluorescent dyes are an accessible option to increase visibility when transgenic approaches are out of reach. In this study, the commercial dye Acridine Orange (AO) was found to be suitable for long-term staining and live imaging of the cnidarian model Nematostella vectensis. Temporary incubation in media containing AO resulted in broad cellular labeling. Individuals stained with AO as zygotes retained the dye throughout embryogenesis, metamorphosis, and for longer than three months of growth, at which point the signal became restricted to subsets of cells. In contrast, staining of zebrafish zygotes with AO resulted in signal decay within the first couple of days of development and preferential accumulation in the yolk sac. AO is retained in N. vectensis adults after amputation and inherited by new tissue during regeneration. Surprisingly, AO was not found suitable for cell tracking via microinjection, as the dye dissipated within minutes of being injected into the cytoplasm of zygotes and blastomeres. Surprisingly, the subcellular distribution of AO signal did not match the pattern expected from it use in mammalian cell lines, where green fluorescence is observed when associated with cellular DNA and red fluorescence when bound to RNA. Instead, long-lived green fluorescence was observed throughout the cell surface and/or in the cytoplasm of N. vectensis stained with AO, whereas red emission was similarly distributed but short lived. Expanding the use of AO as a visualization tool will facilitate future studies of cnidarians and other underexplored animal models.

developmental biology↗

Cytoplasmic polyadenylation is an ancestral hallmark of early development in animals

Differential regulation of gene expression has produced the astonishing diversity of life on Earth. Understanding the origin and evolution of mechanistic innovations for control of gene expression is therefore integral to evolutionary and developmental biology. Cytoplasmic polyadenylation is the biochemical extension of polyadenosine at the 3-end of cytoplasmic mRNAs. This process regulates the translation of specific maternal transcripts and is mediated by the Cytoplasmic Polyadenylation Element Binding Protein family (CPEBs). Genes that code for CPEBs are amongst a very few that are present in animals but missing in non-animal lineages. Whether cytoplasmic polyadenylation is present in non bilaterian animals (i.e., sponges, ctenophores, placozoans, cnidarians) remains unknown. We have conducted phylogenetic analyses of CPEBs and our results show that CPEB1 and CPEB2 subfamilies originated in the animal stem lineage. Our assessment of expression in the sea anemone, Nematostella vectensis (Cnidaria), and the comb jelly, Mnemiopsis leidyi (Ctenophora), demonstrates that maternal expression of CPEB1 and the catalytic subunit of the cytoplasmic polyadenylation machinery (GLD2) is an ancient feature that is conserved across animals. Furthermore, our measurements of poly(A)-tail elongation reveal that key targets of cytoplasmic polyadenylation are shared between vertebrates, cnidarians, and ctenophores, indicating that this mechanism orchestrates a regulatory network that is conserved throughout animal evolution. We postulate that cytoplasmic polyadenylation through CPEBs was a fundamental innovation that contributed to animal evolution from unicellular life.

evolutionary biology↗