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Each time a cell divides, its DNA is duplicated in order that the 2 daughter cells have the identical genetic materials as their father or mother. Which means thousands and thousands of instances a day a biochemical surprise takes place within the physique: the copying of the DNA molecule. It’s a high-precision job carried out by particular proteins and contains methods to guard towards potential errors that would result in illnesses comparable to most cancers.
Certainly one of these anti-failure methods has simply been found by researchers within the DNA Replication Group on the Spanish Nationwide Most cancers Analysis Centre (CNIO), led by Juan Méndez. It’s based mostly on a protein that ensures that DNA is copied solely as soon as, appropriately, and never twice or extra.
When a area of DNA is over-replicated, breaks are created within the molecule, and the chance of a cancer-related gene being over-expressed will increase (whether it is within the over-replicated area); its unfavorable affect on the functioning of the cell would then be better and it could possibly be the beginning of a most cancers.
Subsequently, avoiding extra replication “prevents DNA injury and reduces the possibilities of oncogenes being amplified,” says Méndez.
Copying a sequence of three billion components with out errors
The DNA molecule has a double-helix construction. To be copied, the 2 strands of the helix are first separated and every one serves as a template for the replication equipment to construct two new double helices. Finishing the method takes hours. In tissues that regenerate very regularly, such because the pores and skin or intestines, cells replicate (and duplicate DNA) virtually repeatedly.
It’s not a easy course of. A human DNA molecule has 3 billion chemical items, the bases-;the well-known letters A, T, C, G. The order through which these letters are organized makes up the genetic data, i.e. the directions that inform the cell to make this or that protein at any given second.
If the directions are wrong-;for instance, if there are mutations-;illness can happen. Subsequently, DNA copying is a essential course of for the organism, which has developed a number of molecular mechanisms to keep away from errors. The one which CNIO researchers have now found entails the RAD51 protein. Its mission, on this context, is to forestall DNA fragments which have already been copied as soon as from being copied once more.
Copying begins in 1000’s of locations directly
DNA copying begins at 1000’s of websites concurrently, that are known as origins within the jargon. The proteins liable for copying connect themselves to those origins and begin working, appearing like micro-machines.
An preliminary system for controlling extra replication was already recognized, which prevents origins from being activated greater than as soon as. Nonetheless, if a second copying course of is mistakenly began, the newly found anti-failure mechanism comes into play, based mostly on RAD51.
Researchers at CNIO noticed that RAD51 quickly binds to the newly synthesized DNA. If the copying course of is inadvertently reactivated, its presence on the brand new DNA (which now serves as a template for copying) turns into a bodily obstacle: the copying equipment can not proceed to advance.
A second brake on re-replication
We noticed that RAD51 acts as a second brake on DNA re-replication.”
Sergio Muñoz, first writer of the research
On this means, “RAD51 prevents genomic duplications that would come up from re-activated origins.”
Of their publication in The EMBO Journal, the authors write that “DNA re-replication may gas carcinogenesis by selling aneuploidy [an incorrect number of chromosomes in the cell] and the formation of heterogeneous cell populations that improve the adaptability of tumor cells.”
The protecting position of RAD51 could also be notably essential in pre-tumoral lesions, the place there’s an elevated danger of over-replication.
Researchers from the College of Zurich additionally participated within the research.
Supply:
Journal reference:
Muñoz, S., et al. (2024). RAD51 restricts DNA over-replication from re-activated origins. The EMBO Journal. doi.org/10.1038/s44318-024-00038-z.
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