Research

New research paper published - novel genetic analysis approach for Leigh Syndrome

Dr David Stroud, a NHMRC Doherty Fellow from our lab, co-lead a study with collaborators from the Murdoch Children’s Research Institute, investigating the genetic underpinnings and proteomic changes of patients with Leigh Syndrome.  

Their research revealed that mutations in the MRPS34 gene, a component of the mitoribosome, leading to severe effects on the protein synthesis of mitochondrial encoded proteins required for mitochondrial respiration and energy production. 

A link to the news post on the BDI homepage can be found here.

The publication in the American Journal of Human Genetics can be found here.

A novel isoform of NDUFV3 revealed

A recent publication from the Ryan Lab has revealed that the complex I subunit exists in two isoforms. Published in FEBS Letters in December of 2016, the paper identifies a second long isoform of the peripheral N-module subunit NDUFV3 which exhibits tissue specific expression patterns.

A novel isoform of the human mitochondrial complex I subunit NDUFV3. Marris G. Dibley, Michael T. Ryan, David A. Stroud, FEBS Lett. 2016 Dec 17. doi: 10.1002/1873-3468.12527 Pubmed

Unravelling the genetic mystery behind mitochondrial disease

Researchers from the Monash Biomedicine Discovery Institute in Melbourne have identified two new genes linked to a major cause of mitochondrial disease. Their research opens the way for better genetic diagnosis of the disease and could also help to identify potential therapeutic targets for treatment.

Mitochondrial disease is an illness that robs its sufferers of energy, and damages muscles and major organs like the brain and heart. About one in 5000 babies – or one Australian baby born each week – are born with a severe form of the disease, which can often lead to an early death.

Dr David Stroud and Professor Mike Ryan from the Biomedicine Discovery Institute headed the research team, with their research published today in Nature.

Professor Ryan said the team identified not only two new genes linked to one of the causes of mitochondrial disease, but also uncovered the importance of 30 protein components in the engine that drives the mitochondria.  

“The fact that so many different genes contribute to the function of our mitochondria explains why so many patients remain undiagnosed – it’s a complex disease,” Professor Ryan said. 

Mitochondria are the powerhouses of our cells, taking sugars and proteins from the food we eat and turning them into energy in a form our body can use. This process gives us more than 90 per cent of the energy we need for our bodies to function properly.

In people with mitochondrial disease, the mitochondria are unable to produce this energy, which can lead to organ failure, and potentially, death.

To unravel the genetic mystery behind a major cause of mitochondrial disease, the researchers studied Complex I, one of the engines that helps drive the mitochondria. Professor Ryan said human Complex I was made up of 30 extra protein components than the Complex I of bacteria.

“This has always been a mystery because both bacterial and human Complex I have the same overall function,” Professor Ryan said.

“Our research shows almost all the additional protein components are critical to human health.”

Using a cutting-edge gene editing technology, called CRISPR/Cas9, the researchers modified a series of cells to have a different genetic make-up – each cell type lacked a unique gene relating to a Complex I protein only found in humans. The method they developed could be used to study more of the genes responsible for mitochondrial disease in laboratories around the world.

Professor Ryan said the extra protein components humans have might keep Complex I more stable than the Complex I found in bacteria.

“This might be necessary because our cells live so much longer than bacteria, which divide every 20 minutes.”

The two new genes the researchers found are involved in building Complex I. Dr Stroud said they used the CRISPR/Cas9 gene editing to show that mutating either of the two new genes they identified disrupted Complex I and mitochondrial function.  

“These genes can now be added to genetic screening panels globally, leading to earlier diagnosis of more people with the disease,” Dr Stroud said.

Australian Mitochondrial Disease Foundation CEO Sean Murray welcomed the research findings as an important step towards improving diagnosis and developing therapeutic techniques and medications to fight mitochondrial disease.

“Earlier diagnosis means earlier intervention that may help patients manage their debilitating symptoms and perhaps slow the insidious progression of their disease,” Mr Murray said.

“Advances in diagnosis of mitochondrial disease benefit families by ending their often prolonged and painful odyssey of tests, misdiagnosis and wrong turns.”

 

Committed to making the discoveries that will relieve the future burden of disease, the newly established Monash Biomedicine Discovery Institute at Monash University brings together more than 120 internationally-renowned research teams. Our researchers are supported by world-class technology and infrastructure, and partner with industry, clinicians and researchers internationally to enhance lives through discovery.

New research article published !

Work from our lab has shown that mutations in the gene for the Complex I assembly protein TMEM126B can result in mitochondrial disease. In collaboration with an extensive international team including the Murdoch Children’s Research Institute in Melbourne and Newcastle University Medical School in Newcastle upon Tyne, genetic and biochemical analysis investigated the outcome of these genetic defects in a number of individuals carrying various mutations. This work further increases the number of genes that can carry mutations resulting in mitochondrial disease and may help with therapeutic interventions in the future.

Congratulations to Dr. Luke Formosa who is shared-first author of this article.

This work was recently published work the journal American Journal of Human Genetics.