Identification of novel genetic modifiers in ß-thalassemia

• Applicant: Professor Dr. Andreas Eckhard Kulozik, Ph.D.
• Co-Applicants: Dr. Dvorah Filon; Professor Dr. Moien Kanaan, Ph.D.; Dr. Ariella Oppenheim
• Subject Area: Pediatric and Adolescent Medicine
• Term: from 2004 to 2010
• Project identifier: Deutsche Forschungsgemeinschaft (DFG) - Project number 5411951

The understanding of the phenotypic variability of genetically homogenous disorders represents a major challenge. In b-thalassemia the b-globin gene is affected by a variety of mutations. The group of patients to be analyzed here is homozygous for a splice site mutation that is common in the Middle East. In contrast to this genetic homogeneity the spectrum of the clinical phenotype ranges from mild anemia to most severe, transfusion-depent anemia. We aim at an understanding of this perplexing clinical variability by using a genetic linkage approach to identify modifying factors and by analyzing the effeciency of an mRNA surveillance mechanism that is referred to as nonsense-mediated decay and represents a candidate genetic modifier of b-thalassemia and other genetic disorders.

• DFG Programme: Research Grants
• International Connection: Israel, Palestine
• Participating Person: Professor Dr. Matthias Hentze