The story that features in NAR

Nucleic Acids Res, Volume 53, Issue 2, 27 January 2025, gkaf006, https://doi.org/10.1093/nar/gkaf006

A very curious part of my PhD work on Dictyostelium discoideum chromatin has been published in Nucleic Acid Research this week. My part was to design a 1D extrusion and polymer model that explains why the “bright dots” are happening at the convergent gene positions (CGPs)

After first seeing this fascinating pattern, I hypothesized that cohesin might be dragged to the CGPs by moving polymerase, following up ideas and findings in bacteria by Hugo and Aafke and in mammals by Ed and Aafke. Turns out, simulations only hold if cohesin is significantly slower than polymerase—a strong assumption that requires further confirmation! 

Although we found substitutions in ATP binding in the ATPase heads of the Dicty cohesin that might destabilize ATP binding and lead to a slower speed, I believe that further research and evidence will be essential to solving the puzzle.

I look forward to further research on Dicty and cohesin variants to determine whether my hypothesis holds.

Convergent gene pairs restrict chromatin looping in Dictyostelium discoideum, acting as directional barriers for extrusion. 

Irina V Zhegalova, Sergey V Ulianov, Aleksandra A Galitsyna, Ilya A Pletenev, Olga V Tsoy, Artem V Luzhin, Petr A Vasiluev, Egor S Bulavko, Dmitry N Ivankov, Alexey A Gavrilov, Ekaterina E Khrameeva, Mikhail S Gelfand, Sergey V Razin.

Nucleic Acids Research, Volume 53, Issue 2, 27 January 2025, gkaf006.
DOI: https://doi.org/10.1093/nar/gkaf006

Share the Post:

Related Posts

preprint: Deciphering the 3D genome organization across species from Hi-C data

I’m pleased to share the results of a project I started during my graduate studies, now beautifully completed by my colleagues.

The study applies a sophisticated method to construct joint embeddings of DNA sequences and Hi-C chromatin organization maps within a shared space. This framework allows for the exploration of chromatin structures with distinct functional characteristics, such as insulation domains, loops, and fountains. Intriguingly, it also enables us to identify DNA sequences associated with specific structural features and even modify chromatin maps by ‘adding’ these elements.

One particularly striking result is the construction of a ‘tree of life’ for chromatin spatial organization. While it bears some similarity to traditional phylogenetic trees based on DNA sequences, there are notable differences that reflect significant evolutionary shifts in mechanisms of chromatin folding.

https://www.biorxiv.org/content/10.1101/2024.11.14.623548v2

Read More