ese genes has
been preserved since the last common ancestor of mammals and chicken,
which lived 310 million years ago. "This study is an excellent example
of the power of comparative genomics to illuminate how human genes are
regulated," says Burge.
"As more genome data becomes available and the technology becomes more
sophisticated, I think we'll find that even more genes are targeted by
microRNAs," predicts Lewis.
In addition, the team discovered some hints about how microRNAs find
their targets.
To produce a protein, the cell first makes a template for that protein
by constructing a molecule called messenger RNA. MicroRNAs inhibit
protein production by associating themselves with particular messenger
RNAs, thereby reducing the amount of protein that's ultimately
produced. In this study, the researchers determined which portion of
the microRNA is most important for this process, and identified
additional determinants in the messenger RNA that are likely to
contribute to recognition by microRNAs.
These findings contribute to the recent interest in potential
therapeutic uses of RNA. For example, using a technique known as RNA
interference, or RNAi, researchers are shutting off genes by delivering
into cells artificial microRNA-like molecules called siRNAs. RNAi has
already transformed how many labs are investigating gene functions, and
siRNAs are being developed for clinical applications. Learning more
about how microRNAs operate in human cells should help scientists to
understand how best to exploit siRNAs for treating disease.
'"/>Source:
Whitehead Institute for Biomedical Research
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