黑料传送门

When a wound does not heal properly, it leaves a scar. Similarly, mutations 鈥� which are permanent changes to genetic code 鈥� are often the result of damaged DNA that has not been properly repaired. Mutations can impede the function of genes and lead to disease and aging, but they are also the source of genetic variety, which allows new traits to emerge and facilitates the evolutionary process. Scientists still do not fully understand why some damaged DNA segments are successfully repaired while others are not. In a new study , researchers from the Weizmann Institute of Science succeeded in identifying which DNA sequences and structures are the preferred targets for several of the most important DNA repair enzymes. The findings from the laboratory of Dr. suggest that these preferences shaped the human genome and could even help explain how cells become cancerous.

Every day, thousands of chemical reactions take place in every living cell, damaging the genome. 鈥淲hen DNA repair systems work properly, they repair most of the damage, but not all of it,鈥� Afek explains. 鈥淭herefore, the rate at which mutations accumulate is a balance between the rate of damage and the rate of repair. This balance varies across different areas of the genome, and we still do not understand why certain mutations manage to accumulate in specific regions. Most studies to date have focused on changes that leave a 鈥榮car鈥� 鈥� a mutation. But to fully understand these changes, we must also consider the genetic 鈥榳ounds鈥� themselves, including those that are repaired without leaving a trace.鈥�

In this new study, Afek鈥檚 team sought to characterize where in the genome repair enzymes succeed and where they are less effective. To do this, they developed a chip with thousands of short DNA molecules attached to it, all carrying the same genetic damage but different surrounding sequences.

“”When DNA repair systems work properly, they repair most of the damage, but not all of it”

鈥淲e discovered that, like a good editor examining every word in its context, the three repair enzymes we tested are sensitive to the exact combination of genetic letters, or bases, surrounding the error site,鈥� says doctoral student Noga Levy from Afek鈥檚 lab, who led the study. 鈥淓ven bases located five positions upstream or downstream on the ladder affect how likely the repair enzymes are to recognize the damage site and bind to it. When we delved into the preferred sequences, we found that they share common structural features. One of the enzymes, for example, preferred sequences that create an exceptionally narrow region in the helical ladder.鈥�

In order to understand why that enzyme prefers a specific structure, the Weizmann scientists joined forces with a research team headed by Prof. Brian P. Weiser from Rowan University in New Jersey to run a computer simulation. They found that one of the enzyme鈥檚 amino acids scans the area surrounding the damage site and is attracted to the negative electrical charge that characterizes narrow regions of the ladder.

Next, they tested whether the preferences of the repair enzymes affected how mutations accumulated in the genome over the course of evolution. A DNA molecule looks like a spiral staircase, in which each step is made of a pair of bases. Under normal conditions, there is a base-pairing match: Base A always pairs with T, and C with G. One of the most common forms of genomic damage occurs when a C base is replaced by a different base, disrupting this pairing. Several of the most important DNA repair enzymes are responsible for identifying and removing the incorrect base. The scientists hypothesized that regions where repair enzymes operate efficiently would retain more C bases, while unrepaired changes would accumulate in other regions. And indeed, they found a correlation of exactly that kind for one of the repair enzymes.

鈥淭his finding paves the way for a better understanding of the course of human evolution,鈥� Afek explains. 鈥淭o identify which genomic changes were adopted by humans to survive a changing environment, we must first understand which changes accumulate naturally due to the preferences of the repair mechanisms.鈥�

Mutations are not only a force driving momentous evolutionary changes over billions of years, but also changes that take place in the body of a single person over the years. Cancerous tumors, for example, stem from a single cell in the body whose accumulated mutations cause it to multiply uncontrollably. 鈥淲e found a correlation between the repair enzymes鈥� preferences and mutational signatures 鈥� patterns of mutations 鈥� in human tumors,鈥� Levy adds. 鈥淥ne possibility is that a process in the bodies of cancer patients damaged the repair enzymes, allowing mutations to pile up in areas that were previously protected. Alternatively, over the course of evolution, the repair enzymes may have adapted to target regions that are inherently more vulnerable. Either way, this reinforces our understanding that repair mechanisms play a key role in how cancer develops.鈥�

This study offers a fascinating new way of exploring the cell鈥檚 DNA repair system, and another project in Afek鈥檚 lab, led by graduate student Noga Carmon, has already expanded the scope to other repair mechanisms. 鈥淯nderstanding how repair mechanisms 鈥榗hoose鈥� their targets opens up all kinds of ways to harness them for our own needs,鈥� Afek says. 鈥淲e already use these enzymes as tools in gene editing. A deeper understanding will allow us to fine-tune these technologies and perhaps even engineer enzymes that provide better genetic protection. Since failures in repair mechanisms are a primary driver of cancer, my hope is that understanding them will pave the way for new, more targeted therapies.鈥�