Viral DNA
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Når vira inficerer os, kan de indlejre små bidder af deres genetiske materiale i vores DNA. Selvom det er sjældent, har inkorporeringen af ​​dette materiale i det menneskelige genom forekommet i millioner af år. Som et resultat af denne igangværende proces udgør viralt genetisk materiale næsten 10 procent af det moderne menneskelige genom. Over tid har langt de fleste virale indtrængende, der indgår i vores genom, muteret til det punkt, at de ikke længere fører til aktive infektioner. Men som videnskabsmænd, der er finansieret af National Institute of Health, har demonstreret, er de ikke helt sovende.

Nogle gange kan disse forskudte sekvenser af virale gener, kaldet "endogene retrovirus" (ERV'er), bidrage til starten af ​​sygdomme som kræft. De kan også gøre deres værter modtagelige for infektioner fra andre vira. Forskere har imidlertid identificeret adskillige tilfælde af virale hitchhikers, der giver afgørende fordele for deres menneskelige værter - fra beskyttelse mod sygdom til at forme vigtige aspekter af menneskelig udvikling, såsom evnen til at fordøje stivelse.

Protecting Against Disease

Geneticists Cedric Feschotte, Edward Chuong and Nels Elde at the University of Utah have discovered that ERVs lodged in the human genome can jump start the immune system.

For a virus to successfully make copies of itself inside a host cell, it needs molecular tools similar to the ones its host normally uses to translate genes into proteins. As a result, viruses have tools meticulously shaped by evolution to commandeer the protein-producing machinery of human cells.

Feschotte and his team recognized that because viruses tend to attack the immune system, they may be particularly adept at manipulating immune system genes. Ancient human genomes may have evolved in response. Feschotte believes it is possible that the genomes of humans (or our ancient ancestors) repurposed viral DNA for their own defense, using it to spur the immune system into action against viruses and other foreign invaders.

"We hypothesized that these ERVs were likely to be primary players in regulating immune activity because viruses themselves evolved to hijack the machinery to control immune cells," says Feschotte.

To investigate their hypothesis, Feschotte and his team used a gene-editing technique called CRISPR to systematically eliminate individual ERV sequences in human cells. After removing one of the sequences, the researchers observed a notable weakening of immune function when the cells were challenged by viral infection. The removal of three other ERV sequences also compromised the immune response.

These findings suggest that each of these ERV elements can activate different gene components of the immune system. The team believes there are thousands more ERV sequences with similar regulatory activities, and it hopes to explore them systematically in future studies.

"We think we've only scratched the surface here on the regulatory potential of ERVs," says Feschotte.

Underscoring the complicated relationship humans have with viruses, strong evidence also exists that in some cases ERVs cause cancer but in other cases they protect against cancer. For example, an ERV called ERV9 can detect cancer-related damage in the DNA of cells in the testis. ERV9 then prompts a neighboring gene to induce the damaged cells to commit suicide. This protective mechanism ensures that the cancer cells will not spread.

Shaping Human Evolution

Scientists have also discovered that viral intruders have driven the evolution of human physiological functions ranging from early development to digestion.

Nearly 20 years ago, scientists identified an ERV-derived gene called syncytin that appears to play a key role in the development of the human placenta. Syncytin originated from a retroviral gene encoding a protein that is embedded in the outer surface of a virus. This protein mediates the fusion of the virions with the host cell membrane, thereby facilitating viral infection. In a remarkable turn of events, the human body has repurposed the viral protein's cell-fusing activities to promote the formation of the layer of cells that merge the placenta and the uterus.

Scientists have also found that viral invaders are critical to humans' ability to digest starch. The insertion of an ERV near the human pancreatic gene for making amylase -- a protein that helps humans digest carbohydrates -- led to the expression of amylase in saliva. The consequent ability to digest starch in the mouth has had profound effects on the human diet, notably a shift toward eating foods like rice and wheat. By helping to kick start digestion in the mouth, amylase relieves some of the burden of breaking down food faced by the small intestine. If this critical enzyme were not excreted in saliva, the small intestine would have more difficulty metabolizing sugars and starches.

More recently, in 2016, a team of U.S. and Israeli researchers reported that a common strategy that host organisms use for nullifying viruses -- bombarding them with mutations -- has helped shape human evolution.

The researchers, led by computational biologist Alon Keinan of Cornell University, in collaboration with Erez Levanon from Bar-Ilan University, study a virus-fighting family of human enzymes called APOBECs. During periods when DNA unzips into two single strands -- when it has been damaged, is in the process of being copied, or is being transcribed into RNA -- the APOBEC enzymes seek out bits of viral DNA. They then systematically strafe the viral DNA -- typically swapping many instances of one DNA base for another -- in order to neutralize pathogens lurking within the host genome.

It's likely that this APOBEC mechanism has also mutated non-viral portions of the human genome. Keinan says the majority of these genetic changes would have done enough damage to cause disease. For the most part, such mutations have been weeded out of the population because they were harmful to survival and reproduction. However, researchers have increasingly linked APOBECs to various cancers.

Keinan's team has shown that these mutations are also occurring in cells that develop into sperm and eggs and so they are inherited by future generations. And not all of the mutations have been detrimental. The genetic changes that survived through evolutionary time -- the ones that did not lead to disease -- are more likely to be beneficial. This insight suggests that the APOBEC anti-viral mechanism has helped shape primate evolution through a variety of yet-to-be-identified beneficial mutations. Keinan's team has reported tens of thousands of such mutations in hominid genomes and is now searching for specific examples that led to changes in function that have contributed to human evolution.

While the search for additional examples of beneficial ERVs and antiviral mechanisms continues, scientists are learning more about viral trespassers with the help of large databases of genomic information from numerous species. They're trying to figure out how viral DNA integrates into host genomes, how ERVs can jump from one host species to another and how to protect people in the case of these rare, but occasionally deadly, events.

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Materials provided by NIH, National Institute of General Medical Sciences (NIGMS). Note: Content may be edited for style and length.