Picture bacteria and viruses locked in an arms race.
For many bacteria, one line of defense against viral infection is a sophisticated RNA-guided "immune system" called CRISPR-Cas. At the center of this system is a surveillance complex that recognizes viral DNA and triggers its destruction. However, viruses can strike back and disable this surveillance complex using "anti-CRISPR" proteins, though no one has figured out exactly how these anti-CRISPRs work--until now.
For the first time, researchers have solved the structure of viral anti-CRISPR proteins attached to a bacterial CRISPR surveillance complex, revealing precisely how viruses incapacitate the bacterial defense system. The research team discovered that anti-CRISPR proteins work by locking down CRISPR's ability to identify and attack the viral genome. One anti-CRISPR protein even "mimics" DNA to throw the CRISPR-guided detection machine off its trail.
The new research was published recently in the journal Cell. If CRISPR complexes sound familiar, that's because they are at the forefront in a new wave of genome-editing technologies. CRISPR (pronounced "crisper") stands for "clustered regularly interspaced short palindromic repeats." Scientists have discovered that they can take advantage of CRISPR's natural ability to degrade sections of viral RNA and use CRISPR systems to remove unwanted genes from nearly any organism.
"Although CRISPR-Cas9 is the 'celebrity' CRISPR system, there are 19 different types of CRISPR systems, each of which may have unique advantages for genetic engineering. Using a high-resolution imaging technique called cryo-electron microscopy, the researchers discovered three important aspects of CRISPR and anti-CRISPR systems.
First, the researchers saw exactly how the CRISPR surveillance complex analyzes a virus's genetic material to see where it should attack. Proteins within the complex wrap around the CRISPR RNA like a grasping hand, exposing specific sections of bacterial RNA. These sections of RNA scan viral DNA, looking for genetic sequences they recognize.
"This system can quickly read through massive lengths of DNA and accurately hit its target," said the senior author. If the CRISPR complex identifies a viral DNA target, the surveillance machine recruits other molecules to destroy the virus's genome.
Next, the researchers analyzed how viral anti-CRISPR proteins paralyze the surveillance complex. They found that one type of anti-CRISPR protein covers up the exposed section of CRISPR RNA, thereby preventing the CRISPR system from scanning the viral DNA.
"These anti-CRISPR proteins keep the bacteria from recognizing the viral DNA," senior author explained and called these anti-CRISPR proteins "exceptionally clever" because they appear to have evolved to target a crucial piece of the CRISPR machinery. If bacteria were to mutate this machinery to avoid viral attacks, the CRISPR system would cease to function. "CRISPR systems cannot escape from these anti-CRISPR proteins without completely changing the mechanism they use to recognize DNA," senior author said.
Another anti-CRISPR protein uses a different trick. Based on its location and negative charge, the researchers believe this anti-CRISPR protein acts as a DNA mimic, fooling CRISPR into binding this immobilizing protein, rather than an invading viral DNA.
"These findings are important because we knew that anti-CRISPR proteins were blocking bacterial defenses, but we had no idea how," said the senior author.
The researchers believe this new understanding of anti-CRISPR proteins may eventually lead to more sophisticated and efficient tools for gene editing. Perhaps anti-CRISPR proteins can be used in CRISPR systems to swoop in to block gene editing -- or researchers could degrade anti-CRISPR proteins to trigger gene editing. "That might work as an on-off switch for CRISPR," senior author said.
CRISPR/anti-CRISPR warfare by bacteria and viruses unraveled!
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