香蕉视频

When 11 year old Naomi Lalandec walked into Dr. Robert Koenekoop鈥檚 clinic at the Montreal Children鈥檚 Hospital of the 香蕉视频 Health Centre (MUHC) with blindness and dwarfism due to Oliver McFarlane Syndrome (OMS), her unknown mutation sparked an international gene hunt. Comparing her genome to others with OMS and Leber congenital amaurosis (LCA), another form of childhood blindness, uncovered a new gene that is critical for vision. What makes this breakthrough exceptional is that it opens up new treatment avenues for OMS and LCA and potentially other retinal degenerative diseases.

鈥淚t was like finding a needle in a haystack,鈥� said Dr. Koenekoop, who is also a researcher at the Research Institute of the MUHC and a Professor of Human Genetics, Paediatric Surgery and Ophthalmology at 香蕉视频. 鈥淚t was so obvious to all of us that this was big; a new gene, a possible new disease pathway, a new treatment avenue.鈥� With ongoing support from the Foundation Fighting Blindness (FFB), Canada鈥檚 largest charity supporting vision research, Dr. Koenekoop has spent more than a decade searching for genes linked to blindness. This search brought together an international team of scientists, including Dr. Michel Cayouette at the Institut de recherches cliniques de Montr茅al (IRCM), Dr. Doris Kretzschmar at the Oregon Health and Science University, Dr. Jacek Majewski from the 香蕉视频 and G茅nome Qu茅bec Innovation Centre and more than 30 others from around the world. Together, the team identified mutations in the PNPLA6 gene in families with retinal degeneration. This is the 20th gene associated with LCA and the first associated with OMS.

Although we鈥檝e known about the PNLPA6 gene for more than 45 years, no one had identified that mutations in this gene can lead to retinal degeneration 鈥� until now. To better understand the role of this gene, the team studied how it functions in fruit flies. They learned that the PNPLA6 gene is expressed and located in photoreceptors (which are the light-sensing cells in the eye) and that mutating the gene causes photoreceptors to die.

To determine what PNPLA6 was doing in photoreceptors, the team did a variety of experiments. They observed that some lipids were elevated in fruit flies with the PNPLA6 mutation, which led them to conclude that PNPLA6 affects phospholipid metabolism. Phospholipids are located in our cell membranes where they influence the membrane鈥檚 shape and functioning. They also influence how cells communicate with each other by determining the signals that are able to pass through cell membranes. When phospholipids stop doing what they are supposed to do, important signals get lost and cells can no longer maintain their structures or respond to their environment.

This novel insight about the role of phospholipid metabolism in photoreceptor biology paves the way for new sight-saving treatments. These potentially game-changing results were published on January 9, 2015 in the prestigious journal Nature Communications.

鈥淲e are thrilled about this new collaboration involving Dr. Koenekoop and Dr. Cayouette,鈥� said Dr. Mary Sunderland, Director of Research & Education at the Foundation Fighting Blindness. 鈥淚n addition to being leading scientists, they are incredibly dedicated members of our community who are bridging the gaps between laboratory science and clinical research.鈥�

Moving forward, the team is already thinking about how they can put their new knowledge to work. They are currently generating animal models of this mutation, which will be essential to study how manipulating phospholipids could generate innovative strategies to treat blindness.

Funding:

Research was supported by the Foundation Fighting Blindness, Canada. This work was also funded in part by grants to Dr. Cayouette from the Canadian Institutes of Health Research and the Brain Canada/W. Garfield Weston Foundation. Dr. Koenekoop is also funded by FORGE Canada, the Canadian Institutes of Health Research and the National Institutes of Health.

听

Partners in research:

This project is a collaboration between Dr. R. Koenekoop from the McGill Ocular Genetics Laboratory at the Montreal Children's Hospital of the 香蕉视频 Health Network, which includes S. Cao, H. Ren, I. Lopez, V. Sun, V. Keser, and A. Khan; the laboratory of M. Cayouette from the Institut de recherches cliniques de Montr茅al (IRCM), including V. Ramamurthy; S. Kmoch, S. Fahiminiya, V. Str谩necky, H. Hartmannov谩, A. P艡istoupilov谩, K. Hoda艌ov谩, L. Piherov谩, and L. Kucha艡 from the Institute for Inherited Metabolic Disorders, First Faculty of Medicine, Charles University in Prague; J. Majewski of the Department of Human Genetics, Faculty of Medicine, 香蕉视频 and Genome Quebec Innovation Center; I. MacDonald from the Department of Ophthalmology and Visual Sciences, University of Alberta; A. Baxov谩 from the Institute of Biology and Medical Genetics, First Faculty of Medicine, Charles University in Prague; R. Chen from the Human Genome Sequencing Center, Department of Molecular and Human Genetics, Baylor College of Medicine; O. G. Povoas Barsottini from the Department of Neurology, Division of General Neurology and Ataxia Unit, Universidade Federal de S茫o Paulo; A. Pyle, H. Griffin, and M. Splitt from the Institute of Genetic Medicine, Newcastle University; J. Sallum from the Department of Ophthalmology, Universidade Federal de S茫o Paulo; J. L. Tolmie from the Clinical Genetics, Southern General Hospital, Glasgow; J. Sampson from the Institute of Medical Genetics, Cardiff University School of Medicine; P. Chinnery from the Institute of Genetic Medicine, Newcastle University; Care4Rare Canada; E. Banin and D. Sharon from the Department of Ophthalmology, Hadassah-Hebrew University Medical Center; S. Dutta and D. Kretzschmar from the Oregon Institute of Occupational Health Sciences, Oregon Health and Science University; R. Grebler and C. Helfrich-Foerster from the Lehrstuhl fuer Neurobiology und Genetik, Universitaet Wuerzburg; and J. L. Pedroso from Department of Neurology, Division of General Neurology and Ataxia Unit, Universidade Federal de S茫o Paulo.

听

Media Contacts

Mary Sunderland听
Director of Research & Education听
Foundation Fighting Blindness
1-800-461-3331 ext. 238
416-360-4200
msunderland [at] ffb.ca

Julie Langelier
Communications Officer
IRCM
514-987-5555
julie.langelier [at] ircm.qc.ca

听听听听听听听听听听听
Julie Robert
Public Affairs and Strategic Planning听
香蕉视频 Health Centre听
514-934-1934 ext. 71381听
julie.robert [at] muhc.mcgill.ca