Lab News

     

04 December 2023

Eryk Duński, MSc, was granted an NCN Preludium 22 grant.

In this project, we plan to employ CRISPR-based enhancer perturbation techniques, which will allow us to verify function of the selected evolutionarily gained putative regulatory elements. This knowledge will shed a new light in the mechanisms that orchestrate gene expression in the evolution of astrocytes. 

For description (PL) click here

     

     

24 May 2024

Katarzyna Ciuba, PhD, was granted an NCN Sonata 19 grant.

In contrast to non-human primates, the human brain is equipped with unique abilities, such as speech or abstract thinking. Proper development and function of the brain require coordinated communication between its cells. Extracellular vesicles (EVs)–small, lipid-made structures, that carry biological cargo, that is produced in the “sender cells” and transported inside EVs to the “recipient cells”, where they control particular processes.


In this project, I am going to explore how astrocytic extracellular vesicles and their content changed in primate evolution. I will combine iPS-based models (iAstrocytes and cortical organoids) with gene editing and transcriptomics to uncover the  differences in exosome cargo between the species and their impact on neuronal development. 


For description (PL) click here

     

07 June 2024

Małgorzata Milewska-Puchała, MSc, was granted an NCN Preludium 22 grant.

The mammalian genome is divided into domains of strong self-contact called topologically associating domains (TADs). The boundaries of TADs are defined by the binding sites of a protein named Ctcf and frequently interact with each other forming a three-dimensional architectural chromatin loops. Deletion of the Ctcf protein, abolish formation of TADs and loops, resulting in disruption of gene expression. The mechanisms underlying the architectural functions of Ctcf are not fully understand and are currently under intense investigation.

Our latest data showed that Ctcf interacts with a panel of specific RNA-binding proteins, in an RNA-dependent manner. The goal of this project is to determine, which RNAs contribute to the consolidation of archritectural chromatin structure during mammalian development. In our project, using biochemistry and molecular biology techniques, we aim to identify the role of selected ncRNAs, in Ctcf biology during cellular development. Our results will provide a better understanding of how three-dimensional genome structure and gene expression are regulated during development.

For description (PL) click here