Unique gene expression mechanism may lead to new virus prevention strategies.
A COLLABORATIVE study involving Kansas State University researchers has discovered a new gene expression mechanism in porcine reproductive and respiratory syndrome (PRRS) virus — an important swine pathogen that costs the U.S. pork industry more than $600 million a year.
The discovery provides a new avenue for scientists to explore strategies to control and prevent the disease, the announcement said.
Dr. Ying Fang, associate professor of diagnostic medicine and pathobiology at Kansas State University, led a study that looked at the unique gene expression mechanism of the PRRS virus. Fang and her colleagues found that a new protein in the virus, nsp2TF, was generated through novel ribosomal frameshifting signals.
The research, "Transactivation of Programmed Ribosomal Frameshifting by a Viral Protein," recently appeared in the Proceedings of the National Academy of Sciences (PNAS).
The study builds on a 2012 PNAS study Fang and her European collaborators conducted while she was at South Dakota State University. In it, the researchers identified the nsp2TF protein in the PRRS virus. The protein is expressed through a new gene expression mechanism called -2 ribosomal frameshifting.
"Frameshifting occurs when a ribosome encounters a 'slippery' sequence and downstream signal in messenger RNA," Fang said. "This causes the ribosome to shift two nucleotides backward, which results in all the genetic codons downstream of the shifted site to be read differently and produce a new protein that has a different function."
With the most recent study, the researchers have shown that this -2 frameshifting requires a PRRS virus protein, nsp1beta. It is the first time a virus's genetic mechanism has been found to require the action of a transacting viral protein rather than an RNA structure to induce a ribosomal frameshifting, which is novel in the protein translation field, the announcement said.
The function of the nsp2TF protein is currently under investigation, Fang said. The protein contains a genetic element that may be responsible for suppressing the pig's immune system.
The newly identified ribosomal frameshifting mechanism may provide an additional antiviral target. Fang's research lab cloned the PRRS virus and then genetically engineered nsp2TF protein knockout viruses.
"These knockout viruses could be potentially used to develop vaccines," Fang said. "Additionally, this novel mechanism of gene expression may also be used by other viruses or in cellular gene expression."