Researchers from the group led by UAB Chair Professor Dr Jordi Surrallés at the Hospital de la Santa Creu i Sant Pau, Barcelona, the Universitat Autònoma de Barcelona and the CIBER of Rare Diseases (CIBERER) participated in a study which has led to the identification of a new gene involved in Fanconi anaemia, a rare genetic disease.
The authors of the study, published in the prestigious The Journal of Clinical Investigation, discovered specific mutations in the RFWD3 gene, related to DNA repair, which are involved in the development of this disorder. For this reason, researchers chose to use next-generation massive sequencing technology in the study.
Fanconi anaemia is a hereditary disease caused by mutations in some of the genes related to DNA repair, a process which is essential for the maintenance of stem cells and the prevention of cancer. People affected by this serious disorder suffer from bone marrow failure, several congenital defects and have more chances of developing solid tumours and haematologic problems.
The authors of the research detected mutations in the RFWD3 gene in a child with Fanconi anaemia. They also confirmed the relation between the mutations and the disorder with functional studies in cell and animal models.
The research was coordinated by Dr Detlev Schindler of the University of Würzburg, Germany. Participating were other researchers from the same university and from the University of Kyoto, as well as the group led by Dr Surrallés, Chair Professor in Genetics at the Universitat Autònoma de Barcelona, head of the CIBERER research group and current director of the Genetics Unit at the Hospital de la Santa Creu i Sant Pau.
Until now, there was knowledge of 21 genes involved in Fanconi anaemia. Three years ago, the research group coordinated by Dr Surrallés had already directed a study which gave way to the…