Universiteit Leiden

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Michelle Willebrands

Leiden chemists discover new ways in which single-celled organisms organise their DNA

It has only recently been discovered that single-celled organisms (bacteria and archaea) also have histones—proteins that structure DNA. Now, Leiden PhD candidate Samuel Schwab has found that the histones in these organisms are much more diverse than previously thought. Schwab and his colleagues describe no fewer than seventeen different groups, each with unique structures and functions. The discovery has been published in Nature Communications.

‘DNA is such a large molecule that it technically doesn’t fit inside a cell,’ explains Samuel Schwab. He is a PhD candidate in the Dame group at the Leiden Institute of Chemistry. ‘That’s why there are proteins that compact the DNA. The most well-known are histones.’ For a long time, it was believed that only complex life forms had histones, until scientists discovered them in archaea and eventually in bacteria (both single-celled organisms without a nucleus). Histones form small spheres, called nucleosomes, around which the DNA wraps.

Structure of a spherical structure of histones (nucleosome; Luger et al. 1997). In blue, the nucleosome; in green, the DNA strands wrapped around it

Unraveling histones with the help of computing power

The DNA of archaea and bacteria, appeared to hold numerous ‘recipes’ that closely resembled those for known histones but, with slight differences. ‘We were very eager to find out what kind of histones these recipes would produce,’ says Schwab. ‘This is quite difficult to do in the lab, but fortunately, three years ago, a smart AI algorithm was introduced: AlphaFold. This programme is very good at predicting protein structures based on the corresponding sequences (recipes) in DNA.’ From an enormous protein database, Schwab collected no fewer than 6,000 DNA sequences that could serve as recipes for yet undiscovered histones in archaea and bacteria. ‘With the help of AlphaFold and the Leiden supercomputer facility ALICE, we predicted the structure of the corresponding histones for all these sequences.’

Simple life forms with unexpected diversity

The histones in archaea and bacteria turned out to be much more diverse than previously thought. Schwab identified a total of seventeen different groups. Some of these were already known, but there were also entirely new structures. The researchers then tested whether the computer was correct. ‘We determined the structure of one of these new groups of histones in the lab,’ says Schwab. ‘It turned out to be almost exactly as the computer had predicted!’

One of the new histone structures. This structure, in blue, can bind to a DNA strand (in green) on both sides. By bridging different sections of the DNA strand, loops can form.

Not just wrapping, but also folding or bridging

Based on the predicted structures, the researchers were able to form hypotheses about how these proteins behave and what they might do with the DNA. Schwab: ‘We saw that there are not only spheres that wrap the DNA, but also other structures that, for example, can fold the DNA or bridge different sections of DNA strands, creating loops.’

‘Also fascinating,’ adds supervisor Remus Dame, ‘was the discovery that some histones don’t seem to bind to DNA, but to membranes. So, they have a function other than DNA organisation. But we still need to investigate that further.’

‘We still know very little about what actually happens inside the cell.’

A glimpse behind the curtain

The research by the Dame group contributes to a better understanding of the evolution of DNA organisation and how different organisms manage their genetic material. Dame: ‘Additionally, this knowledge helps us interpret DNA data and measurements. We still know very little about what actually happens inside the cell.’ Schwab agrees: ‘There’s still much to learn about the role of these histones. Discovering these new variants is just the beginning.’

Further reading

Schwab, S., Hu, Y., van Erp, B. et al. Histones and histone variant families in prokaryotes. Nat Commun 15, 7950 (2024). https://doi.org/10.1038/s41467-024-52337-y

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