Grygoriy Zolotarov

Grygoriy Zolotarov
Centre for Genomic Regulation | CRG · Systems Biology

M.D.

About

10
Publications
1,914
Reads
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97
Citations
Additional affiliations
October 2019 - October 2020
Max Delbrück Center
Position
  • Intern
Description
  • Mapping and understanding RNA biology in a common octopus.
July 2019 - September 2019
Centre for Genomic Regulation
Position
  • Intern
Description
  • During this internship, I have been analyzing single-cell RNAseq data from a sea anemone Nematostella to learn how it builds up its nervous system.
July 2017 - August 2017
Weizmann Institute of Science
Position
  • Intern
Description
  • Short stay in Ravid Strausmann lab.
Education
October 2017 - October 2021
Charles University in Prague
Field of study
  • Biology
October 2014 - October 2021
Charles University in Prague
Field of study
  • General Medicine

Publications

Publications (10)
Preprint
Full-text available
A prevailing problem in evolutionary biology is elucidating the genotype-phenotype map that characterizes how genomic activities regulate different aspects of organismal morphology and their variability in both space and time. Here, we explore potential causality between genome content and both morphological complexity and disparity by compiling th...
Article
The circular RNA (circRNA) Cdr1as is conserved across mammals and highly expressed in neurons, where it directly interacts with microRNA miR-7. However, the biological function of this interaction is unknown. Here, using primary cortical murine neurons, we demonstrate that stimulating neurons by sustained depolarization rapidly induces two-fold tra...
Preprint
Full-text available
Incomplete gene models can negatively impact single-cell gene expression quantification. This is particularly true in non-model species where often 3' ends are inaccurately annotated, while most single-cell transcriptomics methods only capturing the 3' transcript region. As a result, many genes are incorrectly quantified or not detected at all. Her...
Preprint
Full-text available
The circular RNA (circRNA) Cdr1as is conserved across mammals and highly expressed in neurons, where it directly interacts with microRNA miR-7. However, the biological function of this interaction is unknown. Here, using primary forebrain murine neurons, we demonstrate that stimulating neurons by sustained depolarization rapidly induced two-fold tr...
Article
Full-text available
Octopuses are mollusks that have evolved intricate neural systems comparable with vertebrates in terms of cell number, complexity and size. The brain cell types that control their sophisticated behavioral repertoire are still unknown. Here, we profile the cell diversity of the paralarval Octopus vulgaris brain to build a cell type atlas that compri...
Article
Full-text available
Soft-bodied cephalopods such as octopuses are exceptionally intelligent invertebrates with a highly complex nervous system that evolved independently from vertebrates. Because of elevated RNA editing in their nervous tissues, we hypothesized that RNA regulation may play a major role in the cognitive success of this group. We thus profiled messenger...
Preprint
Soft-bodied cephalopods such as the octopus are exceptionally intelligent invertebrates with a highly complex nervous system that evolved independently from vertebrates. Because of elevated RNA editing in their nervous tissues, we hypothesized that RNA regulation may play a major role in the cognitive success of this group. We thus profiled mRNAs a...
Preprint
Full-text available
Octopuses are mollusks that have evolved intricate neural systems comparable with vertebrates in terms of cell number, complexity and size. The cell types within the octopus brain that control their amazingly rich behavioral repertoire are still unknown. Here we profile cell diversity of the paralarval Octopus vulgaris brain to build a comprehensiv...
Article
Full-text available
Transposable elements (TEs) have been seen as selfish genetic elements that can propagate in a host genome. Their propagation success is however hindered by a combination of mechanisms such as mutations, selection, and their epigenetic silencing by the host genome. As a result, most copies of TEs in a given genome are dead relics: their sequence is...

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