Scientists have pinpointed for the first time the genetic cause in some people of Emery-Dreifuss muscular dystrophy (EDMD).
The international research team led by the University of Leicester say the finding of two target genes opens the possibility of developing drugs to tackle the disease in these patients. Their work has been published in the journal PLOS Genetics.
The research was funded by The Wellcome Trust and was only possible by the University of Leicester team collaborating with groups in Germany (University of Greifswald), Italy (Institute of Molecular Genetics, Bologna, Italy) and the USA (Columbia University).
To date, only six genes have been linked to EDMD. Despite rigorous screening, at least 50% of patients with EDMD have no detectable mutation in the 6 known genes. Now the breakthrough study has discovered two more genes linked to the disease.
Lead researcher at Leicester, Dr Sue Shackleton, senior lecturer in Biochemistry, said: "We are really excited to have identified mutations in two new genes -- SUN1 and SUN2 -- that are responsible for causing some cases of the muscle wasting disease Emery-Dreifuss muscular dystrophy.
"Emery-Dreifuss muscular dystrophy (EDMD) is an inherited condition that affects around 1,000 people in the UK. It involves muscle wasting and stiffening of the joints. These symptoms usually begin in early childhood and worsen over time, so that many patients have significantly reduced mobility later in life.
"By adulthood, most individuals also develop heart problems that result in an abnormal heartbeat and a high risk of sudden cardiac arrest – the main treatment for this is insertion of a pacemaker. At the moment there is no cure for this disease and no effective treatment for the muscle wasting and joint stiffening."
Dr Shackleton said that in some individuals, EDMD is caused by mutations in one of several genes that are responsible for producing proteins that form a structural support network, or "scaffold," for each cell's nucleus – the compartment that contains the DNA. The reason why mutations in these genes cause this disease is not fully understood, but one theory proposes that the mutations weaken the scaffold structure, leading to damage and death of muscle cells as they continually contract and relax.
However, in up to 50% of individuals with EDMD, no mutation has been identified in any these genes.
Dr Shackleton said: "Our research has identified two new genes, SUN1 and SUN2, that are responsible for causing EDMD in some of these individuals. The proteins produced by these genes also form part of the structural scaffold of the nucleus. Importantly, we have identified a novel way in which these mutations act in muscle cells.
"Our research has shown that the mutated SUN1 and SUN2 proteins interfere with connections between the nucleus and the rest of the cell and that this results in abnormal positioning of the nuclei within the muscle cells. The nuclei are normally anchored at the edges of muscle cells, probably so that they do not get in the way of the main structures of the cell that are involved in muscle contraction. Incorrect positioning could further damage the nuclei and could also impair muscle contraction, leading to the muscle wasting and weakness seen in EDMD sufferers.
