The main findings and methods
In the study's first step, the researchers used "microarrays" made of glass slides containing flatworm genes. The microarrays contained 1,640 flatworm genes out of 13,000 to 18,000 believed to exist. By exposing the slides to dye-tagged genetic material from various portions of the flatworm, the scientists were able to identify which genes were active or "expressed" in the head. The most active gene in the head was ndk.

The scientists confirmed ndk's activity in the head using a technique called "whole-mount in situ hybridization" developed for flatworms by Agata. A flatworm is killed and injected with a genetic "probe" attached to dye. The dye showed the ndk gene was active in the worm's head.

Next, the researchers used a method called "RNA silencing" or "gene silencing" to deactivate the ndk gene, show what goes wrong without it and thus learn its normal function.

Before moving to the University of Utah in 2001, Sánchez Alvarado worked at the Carnegie Institution of Washington, where in 1999 he published a study showing that flatworm genes could be deactivated using gene silencing. A gene works by carrying the blueprint or code to produce a protein. Gene silencing involves injecting an organism with genetic material known as double-stranded RNA, which stops the gene from making a protein.

Sánchez Alvarado says he and his colleagues initially thought that silencing the ndk gene would leave decapitated flatworms unable to regenerate a head. They were surprised when deactivating ndk instead prompted development of brain material throughout the body.

"We saw an expansion of the brain and the appearance of brain material throughout the worm," he says. "We saw brain in the tail."

Silencing the ndk gene also produced flatworms with more than the normal pair of primitive eyes known as "eyespots." So not only did brain material develop everywhere, but extra working eyespots appeared halfway down the flatworms' bodies.

Technical details on how the gene works
The study also investigated how the ndk or "brains everywhere" gene works, revealing that it produces a protein quite similar to "fibroblast growth factor receptors" (FGFRs) in organisms ranging from flatworms to humans.

Fibroblast growth factor or FGF promotes the proliferation and growth of cells and their development into various kinds of cells. Flatworms are able to regenerate missing heads, tails or other body parts because they have "totipotent" stem cells, which are cells that can develop into any kind of cell within the organism.

For FGF to promote cell development, it must attach to receptors on a cell so the cell receives and carries out the order to develop and grow. These receptors are the FGFRs.

The study showed that the ndk gene produces a protein, called NDK, that resembles the FGFRs, but with one important difference: when a growth factor attaches to NDK, the orders to grow and develop are not carried into the cell.

Sánchez Alvarado believes the ndk gene uses that difference to prevent brain material from developing outside the flatworm's head. When a flatworm is cut up and starts to regenerate, the growth factor attaches to receptors in the head so the brain develops. But the ndk gene makes the NDK protein, which acts like a sponge that absorbs growth factor so it cannot spread outside the head and make brain matter develop elsewhere.

When the ndk gene was silenced or deactivated, brain material developed elsewhere in the worm's body. Sánchez Alvarado believes that is because growth factor was not absorbed by NDK in the head, and thus spread throughout the body to induce formation of brain matter.

The researchers showed the ndk gene indeed interacts with growth factor receptors. The scientists prevented those receptors from being produced in the flatworm's body. So even when the ndk gene was silenced and growth factor could spread throughout the flatworm's body, there were no receptors to which it could attach. Thus brain matter did not develop outside the head.

Sánchez Alvarado says ndk is the flatworm equivalent of the human fibroblast growth factor receptor gene known as fgfrl1. What that gene does is unknown. Flatworm and human brains are so different that the human gene probably is not involved in keeping our brains in our skulls, he says. The study suggests the human gene likely "has something to do with central nervous system development in people, but what we don't know."

Another part of the study involved frog embryos instead of flatworms. That is because scientists cannot yet genetically engineer a flatworm to add an extra ndk gene. The researchers genetically engineered early frog embryos to have too much of the gene. Those embryos failed to develop certain body tissues that normally develop due to fibroblast growth factors. So the experiment provided more evidence that the ndk gene controls brain and tissue development by soaking up growth factor.

In addition to Sánchez Alvarado and Agata, co-authors of the study are Francesc Cebria, Chiyoko Kobayashi and Yoshihiko Umesono of the Center for Developmental Biology in Kobe; Masumi Nakazawa, Katsuhiko Mineta, Kazuho Ikeo and Takashi Gojobori at Japan's National Institute of Genetics; and Mari Itoh and Masanori Taira at the University of Tokyo.

This news release and downloadable, high-resolution photos are available at:
http://www.utah.edu/unews/releases/02/oct/brains.html