RNA Silencing: Defense and Counterdefense
Dr. Vance's research is directed toward understanding the molecular basis of plant defense against viruses. The model system currently used in the lab is the synergistic disease caused by a mixed infection of tobacco with potato virus X (PVX) and any of a number of related viruses belonging to the genus Potyvirus, for example tobacco etch virus (TEV). Plants infected singly with either PVX or TEV show low levels of disease symptoms. However, in combination, the two viruses cause a devastating disease, and the dramatic increase in host symptoms is correlated with a large increase in the accumulation of PVX in the infected tissues, but no corresponding increase or decrease in the level of TEV. Such synergistic diseases are common in plants and frequently involve a member of the Potyvirus genus as one of the members of the synergistic pair. Our work with the PVX/potyviral interaction has shown that the synergistic increase in PVX accumulation and the correlated increase in host symptoms does not require replication of the potyvirus, but is mediated by expression of a single potyvirus gene product, the helper-component proteinase (HC-Pro) (see Vance et al, 1995). We further found that expression of HC-Pro in transgenic plants allowed a broad range of unrelated viruses to accumulate to a higher level (see Pruss et al., 1997). This led us to hypthesize that HC-Pro worked by interfering with a general anti-viral defense pathway. We proposed at that time that the anti-viral pathway suppressed by HC-Pro was RNA silencing.
RNA silencing is a remarkable type of gene regulation based on sequence-specific targeting and degradation of RNA. The term refers to related pathways found in organisms as diverse as fungi (quelling), plants (post-transcriptional gene silencing, PTGS), protozoans, and a variety of animals including C. elegans, Drosophila, and mice (RNA interference, RNAi). In these organisms, the process is characterized by conserved genes and biochemical features. One key conserved feature is that the induction of RNA silencing involves dsRNA. In plants, RNA silencing may have evolved as a defense against viruses, many of which replicate via dsRNA intermediates. An intriguing aspect of RNA silencing is that it may be triggered locally and then spread throughout the organism via a mobile silencing signal. The identity of the mobile signal remains unknown, but it is thought to incorporate a nucleic acid component to account for the sequence specificity of the process. Another interesting feature of silencing is the accumulation of small RNAs (called siRNAs) that incorporate into the silencing complex and act as guide RNAs to to target specific molecules for destruction.
Our work with viral synergism and HC-Pro is consistent with the idea
that RNA silencing is an anti-viral defense. In recent work we have used
HC-Pro as a tool to understand the mechanism of gene silencing. We show
that HC-Pro suppresses several classes of RNA silencing. In the case of
silencing induced by a single copy sense transgene, we established that
HC-Pro acts downstream of the mobile silencing signal and interferes with
the accumulation of the small RNAs (see Mallory et al., 2001). We have
identified several cellular proteins that interact with HC-Pro in the
yeast two-hybrid system. Studies of the role of these proteins in RNA
silencing are providing clues about the mechanism and regulation of the
silencing pathway. One HC-Pro-interacting protein is a calmodulin-related
protein called rgs-CaM, that also suppresses RNA silencing when over-expressed
in plants (see Anandalakshmi et al., 2000). The emerging view is that
RNA silencing is part of a sophisticated network of interconnected pathways
for cellular defense, RNA-surveillance, and development, and may become
a powerful tool to experimentally manipulate gene expression (see Vance
and Vaucheret, 2001).