Target 5000: Target Capture Sequencing for Inherited Retinal Degenerations

G C A T T A C G G C A T genes Article Target 5000: Target Capture Sequencing for Inherited Retinal Degenerations Adrian Dockery 1, *, Kirk Stephenson 2 , David Keegan 2 , Niamh Wynne 3 , Giuliana Silvestri 4,5 , Peter Humphries 1 , Paul F. Kenna 1,3 , Matthew Carrigan 1,† and G. Jane Farrar 1,† 1 2 3 4 5 * † The School of Genetics & Microbiology, Trinity College Dublin, Dublin 2, Ireland; (P.H.); (P.F.K.); (M.C.); (G.J.F.) The Mater Misericordiae University Hospital, Dublin 7, Ireland; (K.S.); (D.K.) The Research Foundation, Royal Victoria Eye and Ear Hospital, Dublin 2, Ireland; Department of Ophthalmology, The Royal Victoria Hospital, Belfast BT12 6BA, Northern Ireland, UK; Centre for Experimental Medicine, Queen’s University Belfast, Belfast BT7 1NN, Northern Ireland, UK Correspondence: Authors contributed equally. Academic Editor: Frans P. M. Cremers Received: 8 September 2017; Accepted: 27 October 2017; Published: 3 November 2017 Abstract: There are an estimated 5000 people in Ireland who currently have an inherited retinal degeneration (IRD). It is the goal of this study, through genetic diagnosis, to better enable these 5000 individuals to obtain a clearer understanding of their condition and improved access to potentially applicable therapies. Here we show the current findings of a target capture next-generation sequencing study of over 750 patients from over 520 pedigrees currently situated in Ireland. We also demonstrate how processes can be implemented to retrospectively analyse patient datasets for the detection of structural variants in previously obtained sequencing reads. Pathogenic or likely pathogenic mutations were detected in 68% of pedigrees tested. We report nearly 30 novel mutations including three large structural variants. The population statistics related to our findings are presented by condition and credited to their respective candidate gene mutations. Rediagnosis rates of clinical phenotypes after genotyping are discussed. Possible causes of failure to detect a candidate mutation are evaluated. Future elements of this project, with a specific emphasis on structural variants and non-coding pathogenic variants, are expected to increase detection rates further and thereby produce an even more comprehensive representation of the genetic landscape of IRDs in Ireland. Keywords: retina; genetics; ophthalmology; retinitis pigmentosa; genomics 1. Introduction Inherited retinal degenerations (IRDs) represent the most frequent cause of vision loss in people of working age. As a result, these conditions have a highly significant impact on quality of life and health-related costs and loss of income. IRDs are an extremely heterogeneous set of conditions associated with the loss of retinal function, and as a group, represent one of the most genetically diverse hereditary conditions. Over 260 genes to date have been implicated in the syndromic and non-syndromic IRDs [1], with a wide range of clinical presentations and rates of progression. As this is a diverse set of conditions with frequently overlapping presentations, it is typically divided into large sub-categories, primarily by specific regions or cell types affected, such as rod photoreceptors, cone photoreceptors or, for example, peripheral versus macular regions of the retina. Retinitis Pigmentosa (RP) is the most common form of IRD, is extremely genetically heterogeneous and affects Genes 2017, 8, 304; doi:10.3390/genes8110304 www.mdpi.com/journal/genes Genes 2017, 8, 304 2 of 21 as many as 1 in 3000 individuals [2,3]. The disease is typically characterized by progressive loss of rod photoreceptor cells, followed by the gradual death of cone photoreceptors and generally involves characteristic features such as pigmentary deposits in the peripheral retina and attenuation of retinal vessels. In contrast, some other forms of IRD can be extremely rare and have a single gene aetiology; gyrate atrophy, for example, is estimated to affect roughly one in a million people [4]. IRDs are currently thought to affect approximately 2.5 million people globally. The vast majority of these individuals have received a diagnosis based on clinical phenotype alone, rather than a genetic diagnosis, if they have been formally diagnosed at all. Clinical trials are in progress for a number of IRDs, however most such trials require patients to have a known causative mutation to participate. Here we present data from Target 5000, an ongoing next generation sequencing (NGS)-based study, which aims to genetically characterise a large national cohort of IRD patients. The most common method chosen for IRD genetic screening is targeted NGS. Although whole-exome sequencing offers the potential to locate disease-causing mutations in novel genes, in practice diagnosis rates in whole-exome and targeted-sequencing studies are similar [5], suggesting that the coding regions responsible for the majority of IRDs have been located. Although whole genome analysis has the potential to discover non-coding disease-causing mutations, the difficulty involved with data interpretation and cost associated with the study increase dramatically. During the course of this study, over 750 individuals from over 520 pedigrees have been sequenced with a targeted NGS panel, focused on exons of 254 IRD-associated genes, in addition to a small number of introns previously reported to harbour splice-altering mutations. Here we present novel mutations primarily from over 200 patients involved in recent recruitment but also resulting from retrospective analysis based on previously recruited patient cohorts [6]. Candidate mutations were detected in over 68% of our analysed pedigrees. This figure includes previously reported pathogenic mutations and numerous novel likely pathogenic variants. Novel variants include large structural variants, point mutations with high predicted pathogenicity, frameshift mutations and splice site mutations. A single pathogenic or likely pathogenic variant was observed in an additional 8% of pedigrees in which the gene in question is known to cause a recessive retinopathy. 2. Materials and Methods 2.1. Patient Identification and Recruitment Probands and other family members were primarily assessed at the Research Foundation of the Royal Victoria Eye and Ear Hospital (Dublin, Ireland) and the Mater Misericordiae University Hospital (Dublin, Ireland). With informed consent, best-corrected visual acuity was assessed using revised 2000 Early Treatment Diabetic Retinopathy Study (ETDRS) charts (Precision Vision, La Salle, IL, USA). Colour vision was examined using the Lanthony desaturated D-15 panel (Gulden Ophthalmics, Elkins Park, PA, USA) under standardised lighting conditions. Goldmann perimetry was used to assess the peripheral visual fields to the IV4e, I4e and 04e targets. Full-field electroretinograms were performed according to the International Society for Clinical Electrophysiology of Vision (ISCEV) sta (...truncated)