Identifying Cis-Regulatory Elements Around The ARMS2 Locus
Principal Investigator
Project Goals
Recent genetics studies have delineated a 23.3 Kb region around the ARMS2 locus that contains DNA sequence variants that are strongly associated with a person's susceptibility to age-related macular degeneration (AMD). We propose to identify all of the photoreceptor-specific gene regulatory elements in this 23.3 Kb region and to test whether sequence variants within these regions found in AMD patients affect the activity of these elements. In this manner it should be possible to determine which sequence variants are likely to cause disease, thus facilitating the genetic diagnosis of AMD.
Project Summary
DNA changes that can predispose patients to age-related macular degeneration (AMD) come in two varieties: those which affect sequences that encode proteins (so-called, 'coding' changes) and those which affect sequences that control the expression of genes ('non-coding' changes). Although a lot is known about 'coding' changes, 'non-coding' changes are relatively poorly understood. Our research aims to develop a better understanding of the effects of 'non-coding' changes on a person's susceptibility to AMD. We plan to first map the location of 'cis-regulatory elements' which control the expression of genes relevant to AMD. Then, we will determine which DNA changes found in AMD patients are associated with changes in the expression of these AMD genes. Once we have successfully completed this research, we should be able to more accurately diagnose AMD and predict which patients are likely to be affected by it by being able to more precisely map the effects of their DNA changes on AMD gene expression. The financial support of the BrightFocus Foundation is critical to furthering our understanding of this devastating disease.
Progress Updates
A short region of the human genome on chromosome 10 is involved in the development of age-related macular degeneration (AMD). Patients that carry certain DNA changes in this region have an increased likelihood of developing AMD. However, the specific cause of this increased risk is unknown.
Dr. Joseph Corbo and colleagues have taken a combined computational and experimental approach to study this region of chromosome 10 which contains two genes— ARMS2 and HTRA1. These researchers have identified DNA patches around these genes which control the expression of HTRA1 in certain support cells within the retina, known as Müller glia. These DNA patches are known as “cis-regulatory elements.” However, patient-associated DNA sequence or “spelling” changes in these elements did not significantly affect expression of the HTRA1 gene in customized assays. Nevertheless, Dr. Corbo's results suggest a possible role for Müller glia in the risk for developing AMD. This finding is important because until now Müller glia cells have not been implicated in AMD despite their key structural and functional roles in the human retina.
Publications
Langmann T, Di Gioia SA, Rau I, Stöhr H, Maksimovic NS, Corbo JC, Renner AB, Zrenner E, Kumaramanickavel G, Karlstetter M, Arsenijevic Y, Weber BH, Gal A, Rivolta C. Nonsense Mutations in FAM161A Cause RP28-Associated Recessive Retinitis Pigmentosa. Am J Hum Genet. 2010 Aug 11. 
Corbo JC, Lawrence KA, Karlstetter M, Myers CA, Abdelaziz M, Dirkes W, Weigelt K, Seifert M, Benes V, Fritsche LG, Weber BH, Langmann T. CRX ChIP-seq reveals the cis-regulatory architecture of mouse photoreceptors. Genome Res. 2010 Aug 6.
First published on: April 15, 2009
Last modified on: December 23, 2024