Mechanism that restores cell function after genome damage

Date:
October 13, 2020
Source:
University of Cologne
Summary:
Researchers have found out how cells can recover their development
and longevity after damage by UV. The discovery may enable new
therapies against premature aging.



FULL STORY ==========================================================================
A research team from Cologne has discovered that a change in the DNA
structure -- more precisely in the chromatin -- plays a decisive role in
the recovery phase after DNA damage. The key is a double occupation by
two methyl groups on the DNA packaging protein histone H3 (H3K4me2). The discovery was made by scientists under the direction of Prof. Bjo"rn
Schumacher of the Cluster of Excellence for Aging Research CECAD, the
Center for Molecular Medicine Cologne (CMMC), and the Institute for Genome Stability in Aging and Disease at the University of Cologne. The specific change enables genes to be reactivated and proteins to be produced after damage: The cells regain their balance and the organism recovers. The protective role of H3K4me2 was identified in experiments with the nematode Caenorhabditis elegans. The study has now been published in the journal
Nature Structural & Molecular Biology.


==========================================================================
The genome in every human cell is damaged on a daily basis, for example in
the skin by UV radiation from the sun. Damage to the DNA causes diseases
such as cancer, influences development, and accelerates aging. Congenital malfunctions in DNA repair can lead to extremely accelerated aging in rare hereditary diseases. Therefore, preservation and reconstruction processes
are particularly important to ensure development and to maintain tissue function. DNA, which is rolled up on packaging proteins -- the histones --
like on cable drums, is regulated by methyl groups. Various proteins are responsible for placing methyl groups on histones or removing them. The
number of groups on the packaging proteins affects the activity of genes
and thus the protein production of the cell.

In experiments with the nematode, the research team showed that after
repairing damaged DNA, two methyl groups were increasingly found on the
DNA packages.

Furthermore, they found that errors in placing these two methyl groups
on the histones (H3K4me2) accelerated the damage-induced aging process,
while increased position of this histone alteration prolongs the lifespan
after DNA damage. By controlling the proteins that either set or remove
these methyl groups, the resistance to DNA damage -- and thus the aging
process of the animals -- could be influenced.

Further analysis of the role of these two methyl groups showed that the enrichment of H3K4 after genome damage with two methyl groups supports
the cells in restoring the balance after DNA damage.

'Now that we know the exact changes in chromatin, we can use this to
precisely limit the consequences of DNA damage,' said Schumacher. 'I hope
that these findings will enable us to develop therapies for hereditary
diseases characterized by developmental disorders and premature aging. Due
to the fundamental importance of DNA damage in the aging process, such approaches could also counteract normal aging and prevent age-related diseases.'

========================================================================== Story Source: Materials provided by University_of_Cologne. Note: Content
may be edited for style and length.


========================================================================== Journal Reference:
1. Siyao Wang, David H. Meyer, Bjo"rn Schumacher. H3K4me2 regulates the
recovery of protein biosynthesis and homeostasis following DNA
damage.

Nature Structural & Molecular Biology, 2020; DOI:
10.1038/s41594-020- 00513-1 ==========================================================================

Link to news story: https://www.sciencedaily.com/releases/2020/10/201013124105.htm

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