Hope Not Hype - Third World Network
Hope Not Hype - Third World Network
Hope Not Hype - Third World Network
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Appendix One: What is a GMO<br />
133<br />
“Modern biotechnology” means the application of:<br />
a. In vitro nucleic acid techniques, including recombinant deoxyribonucleic acid (DNA) and<br />
direct injection of nucleic acid into cells or organelles…<br />
– transformation of an organism by any in vitro modified RNA would constitute the creation<br />
of a GMO because RNA is a nucleic acid. The Protocol does not make a distinction<br />
between chemical and gene, nor does it invite one to be made.<br />
A distinction between genetic material and chemicals is the ability of the former<br />
material to contribute to its own amplification. Amplification is often taken as an indicator<br />
of a material’s ability to carry traits across generations or through infectious transfer (e.g.,<br />
such as a virus). In contrast, chemicals do not participate directly as co-factors in an<br />
amplification pathway. While both RNA and some antibiotics (e.g., rifampicin) can change<br />
patterns of gene expression, the former is not equivalent to the latter in classification as a<br />
chemical because it can be amplified by “can be copied” as well as “copies itself” pathways.<br />
RNA can be amplified in the sense of “can be copied” through biochemical pathways that<br />
organize around the existence of a particular dsRNA molecule and produce new equivalent<br />
dsRNA molecules not by polymerization but by degradation of other RNA molecules in<br />
the same cell. RNA can cause the transfer of characters and traits in the sense of “copies<br />
itself” through dsRNA-mediated de novo methylation of DNA and histones; that<br />
methylation is perpetuated by still other biochemical pathways.<br />
Gene silencing is a trait that can amplify but not by the same biochemical pathways<br />
as DNA. Evidence of this amplification is:<br />
[Infectious transfer:] The small amounts of dsRNA required for gene silencing and larval<br />
mortality suggest an amplification pathway in which ingested dsRNAs are processed to<br />
siRNAs, presumably within insect gut epithelial cells, which may prime the synthesis of<br />
more abundant secondary siRNAs…Northern blot analysis of total RNA from whole WCR<br />
larvae revealed almost complete suppression of targeted transcripts from several housekeeping<br />
genes, suggesting systemic spread of silencing beyond gut epithelial cells, the presumed<br />
initiation site of the RNAi response (Baum et al., 2007, p. 1323).<br />
One of the most intriguing aspects of RNA silencing is that it is non-cell-autonomous: in<br />
both plants and Caenorhabditis elegans it can be induced locally and then spread to distant<br />
sites throughout the organism. The systemic spread of silencing reflects the existence of an<br />
as yet unidentified mobile silencing signal as an integral component of the RNA silencing<br />
pathway…In grafting experiments, systemic silencing was transmitted across a graft junction<br />
from spontaneously silenced transgenic tobacco rootstocks to isogenic scions that had not<br />
silenced spontaneously (Mlotshwa et al., 2002, pp. S289-S290).<br />
The transmission of PTGS also occurred when silenced stocks and non-silenced target scions<br />
were physically separated by up to 30 cm of stem of a non-target wild-type plant, indicating<br />
long-distance propagation (Vaucheret et al., 2001, p. 3084).