Misfolded proteins serve as 'inherited memory' of toxic insults

Misfolded proteins serve as 'inherited memory' of toxic insults
The E. coli bacterium was used to test the effects of protein aggregates as a protection against toxic stresses. Credit: NIAID, Flickr, CC-BY

Protein aggregates have a bad reputation in conditions such as Alzheimer's disease and Parkinson's disease, but in bacteria, inheritance of aggregates by daughter cells may help protect against the same toxic stresses that triggered them in parental cells, according to a new study publishing 28 August in the open access journal PLOS Biology, by Sander Govers, Abram Aertsen, and colleagues at KU Leuven, Belgium. The aggregates thus serve as a kind of inherited memory, protecting offspring against the challenges experienced by their ancestors.

Protein misfolding is a risk for any cell, and is especially common when the cell is exposed to heat, oxidative stress, or other insults. Misfolded proteins that are not immediately disposed of often clump together to form long-lived aggregates. Such aggregates are seen in neurodegenerative diseases such as Alzheimer's disease and Parkinson's disease, where they are thought to contribute to the neurodegenerative process. Aggregates also form in bacteria such as Escherichia coli, found in the gut, and have been thought to be damaging to these as well. But some evidence suggests aggregates may also play a protective role, at least in , leading the authors to ask whether they might confer some benefit in .

To test this, they induced aggregates in E. coli by exposing the cells to heat, antibiotics, or peroxide. When a given bacterial cell subsequently divided, the aggregate it contained was segregated into only one of the two . After multiple generations, cells were again exposed to aggregate-inducing stressors. Those sibling cells containing inherited aggregates displayed improved survival and faster recovery than those without them. The same survival benefit could be induced by expression of an inert aggregation-prone protein, suggesting it was the presence of an aggregate, rather than its composition, that improved survival. The authors found that cells with aggregates inherited more of the proteins that protect against stresses, even before exposure to those stresses, which they suggest accounts for the increase in survival.

"Our findings indicate the potential of protein aggregates to improve cellular robustness, in contrast to the prevailing view that they are inevitably detrimental to cellular health," said Aertsen. "Moreover, because protein can persist and be inherited for many generations as a functional physical relic of an ancestral insult, they can serve as long-term epigenetic memory in prokaryotes."


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More information: Govers SK, Mortier J, Adam A, Aertsen A (2018) Protein aggregates encode epigenetic memory of stressful encounters in individual Escherichia coli cells. PLoS Biol 16(8): e2003853. doi.org/10.1371/journal.pbio.2003853
Journal information: PLoS Biology

Citation: Misfolded proteins serve as 'inherited memory' of toxic insults (2018, August 28) retrieved 4 April 2020 from https://phys.org/news/2018-08-misfolded-proteins-inherited-memory-toxic.html
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