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Prestigious Wilson Award Goes To Yale Cell Biologist Joel Rosenbaum

Joel Rosenbaum, professor in the Department of Molecular, Cellular and Developmental Biology (MCDB) and faculty member at Yale since 1967, will be awarded// the prestigious 2006 E. B. Wilson Medal, the American Society for Cell Biology’s highest honor for scientific research in cell biology.

The medal is indeed a recognition of Rosenbaum’s contribution on the assembly, maintenance and function of fine, hair-like cell organelles, called cilia and flagella (interchangeable terms), which extend from the cell surface.

Recently, Rosenbaum and his students and colleagues have shown that the cilia are fundamental to the pathogenesis of one of the most prevalent of human diseases, PKD, polycystic kidney disease, forms of which can affect as many as 1 in 500 people.

Rosenbaum has produced much of his groundbreaking research by studying cilia/flagella in single celled protistans, principally the bi-flagellate alga, Chlamydomonas. Cilia are best studied in organisms like Chlamydomonas because their structure has been conserved even to humans, and they can be grown in quantity to isolate flagella in large amounts. Further, their cell division is easily synchronized and the genome sequence of Chlamydomonas and the flagellar “proteome,” or complete catalogue of proteins, has been published.

Using this organism, Rosenbaum designed systems to study flagellar growth and regeneration. In some of his initial studies, as a post doctoral fellow at the University of Chicago, Rosenbaum showed that flagella grew and elongated by adding on new subunits to their tips, distant from the cell body where the flagellar proteins are synthesized.

When listening to Rosenbaum present this “flagellar tip growth” story in the mid-1970s, former Yale Professor and Nobel laureate George Palade suggested that there “must be elevators in the flagella” carrying subunits from their site of synthesis in the cell body to the tip of the flagella where a ssembly takes place.

Finally, in 1992, using new high-resolution microscopes in the laboratory of Paul Forscher, who had recently joined the department, Rosenbaum’s graduate student, Keith Kozminski, was first able to observe these elevators. He saw particles moving up and down the length of the flagella, between the membrane and the microtubule-based core of the flagella. They named the process intraflagellar transport (IFT).

These initial observations led to biochemical and genetic studies showing that molecular motors controlled movement of the IFT particles. When the motors were stopped, flagella would not form, and already-formed flagella became shorter. They also showed that the IFT particles served as transports, carrying prefabricated parts of the flagellar core to the tip for assembly, and recycling turnover products from the tip back to the cell body. Over the next several years, IFT particles were isolated, their polypeptides identified, and many of the genes for IFT cloned.

When the IFT genes were compared with the various available “on line” gene libraries, they were surprised to find that a sequence matching one Chlamydomonas IFT gene, called “IFT88” was in the mouse genome and was the gene which was defective in the then-current mouse model of polycystic kidney disease (PKD).

The relationship between an IFT particle gene that would block flagella assembly in Chlamydomonas when mutated and produce PKD in the mouse model seemed remote. Few had paid attention to the fact that the cells forming the kidney tubules each had a single non-motile “primary” cilium pointing toward the center of the tubule.

When Rosenbaum and his colleagues Gregory Pazour and George Witman at University of Massachusetts Medical School examined kidney tubules of the PKD mutant mouse with the scanning electron microscope, they found that the cilia were either short or missing. They also provided conclusive evidence for the im portance of cilia in the PKD pathology by demonstrating that the polycystins, gene products of the PKD genes, were located on these cilia. Because cilia were related directly to the disease, this became known as the “ciliary hypothesis of PKD.”

“Researchers at the NIH and Yale Medical School have now shown that these cilia bend when urine flows down the tubules, admitting calcium through the polycystins, which are mechano-receptors in the ciliary membrane. Through a signaling pathway, the calcium represses cell division,” said Rosenbaum. “If calcium does not flow in, because the cilia are missing, or the polycystins on the membrane are missing or ineffective, a signal is sent to the nucleus and the tubule cells divide—and continue to divide. PKD is, therefore, a cancer of the kidney, where cells that should not be dividing start to divide because of a defect in a signaling pathway starting at the cilium”

This sensory role of primary non-motile cilia has now become the model for many other diseases and syndromes, all of which trace back in many different tissues to defects in receptors or channels on the ciliary membrane, or to the complete lack of the cilium due to a defect in the IFT process.

Rosenbaum’s laboratory is now working on the connection between cilia and the cell cycle. “These primary non-motile cilia must resorb prior to cell division or the cell will not divide,” he said. Their latest work shows that when the amount of one of the IFT polypeptides, a small G protein, is decreased, the cell cycle is severely inhibited. This IFT small G-protein is a direct link between cilia and the cell cycle. In a normal cell cycle, the protein decreases, taking all the other IFT polypeptides with it, causing the cilia to shorten, and permitting the ciliary basal bodies/centrioles to migrate to the center of the cell to form the mitotic apparatus. Following chromosome separation, the amount of this IFT protein again increases, and the ce ll divides. If the amount of the IFT protein is kept low experimentally, the cells will not divide, and will die.

Understanding the IFT process has also led to discoveries on causes of conditions like situs inversus, a condition in which the heart or other organs grow on the wrong side of the body’s midline during embryonic development. Rosenbaum’s colleague in pediatric cardiology, Associate Professor Martina Brueckner, has shown that the presence of cilia in the embryonic nodal region is directly related to this condition; if the cilia are missing or not functioning, situs inversus results. In the mutant mouse with defective or missing cilia, situs inversus occurs as well as PKD in many cases. Many of these mice are also blind, because the rod outer segments of the retina form from cilia during embryogenesis, and are maintained in adults by IFT in a piece of the cilium in the adult rod cell.

Finally, a complex of diseases called Bardet-Biedl Syndrome (BBS), which can manifest itself in diabetes, polydactyly, and obesity, all stem from defects in the cilia or the ciliary basal body/centriole. “It seems as though, each month a new disease is shown to have its origin in these oft-neglected cell organelles,” said Rosenbaum.”

The exciting thing, Rosenbaum feels, is that all of this work relating to human diseases began with studies initiated on flagellar assembly in a green alga. It is an example of the continuity of life, or as Rosenbaum says, “If you’ve seen one cilium, you have [almost] seen them all.”

Rosenbaum is the seventh member of the Yale faculty to receive the Wilson Award, In 2005, Joan A. Steitz, Sterling Professor of Molecular Biophysics & Biochemistry and Investigator of the Howard Hugnes Medical Institute, received the award for her work on small nuclear ribonucleoproteins, known now as SnRNPs. In 2004, Thomas D. Pollard, Sterling Professor and Chair of the Department of Molecular Cellular & Developmental Bi ology, received the award for his pioneering work on the molecular basis of cell movement. Other past Yale faculty who have received the award are George Palade and Marilyn Farquhar (University of California, San Diego), Joseph Gall (Carnegie Institute of Embryology), and Bruce Nicklas (Duke University). br>

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