When cut, a planarian flatworm can regenerate a new head, new tail or even entire new organisms from a tiny fragment of its body--a phenomenon that has puzzled researchers for more than 100 years.
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Now, scientists in the lab of Peter Reddien, a member of the Whitehead Institute for Biomedical Research and an MIT assistant professor of biology, have discovered a gene required for proper decisions about head-versus-tail polarity in regenerating flatworms.
Their results, published in the Dec. 6 issue of Science online, could help explain how regenerating animals "know" what missing tissues to make.
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"Evolution has selected for mechanisms that allow organisms to accomplish incredible feats of regeneration," and planaria offer a dramatic example, Reddien said. "By developing this model system to explore the molecular underpinnings of regeneration, we now have a better understanding of … the process."
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The researchers used a technique called RNA interference to screen a group of genes known to be involved in animal development.Â
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"We discovered that inhibiting the gene Smed-beta-catenin-1 caused animals to regenerate a head instead of a tail at the site of the wound," said Christian Petersen, Whitehead postdoctoral fellow and lead author on the paper. "This resulted in a worm that possessed two oppositely facing heads. Smed-beta-catenin-1 is the first gene found to be required for this regeneration polarity."
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Genes very similar to Smed-beta-catenin-1 are found in animals ranging from jellyfish to humans, and they have been implicated in posterior tissue specification in frogs, sea urchins and many other animals.Â
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The researchers then went on to study the expression of a family of genes associated with regeneration. They found that different members of the Wnt gene family were active at different locations across the planarian's head-to-tail axis. These results suggest that Smed-beta-catenin-1 may be active in the tail region and inhibited in the head region by the regulated expression of these Wnt genes.
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Additionally, the researchers found that Smed-beta-catenin-1 plays a role in ongoing cell replacement in planaria that have not been challenged to regenerate. When the gene was inhibited, these animal's tails began changing into heads.
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The researchers hope that future work on regeneration polarity and Smed-beta-catenin-1 will yield a better understanding of the molecular mechanisms of regeneration.