Dissecting the role of EYS in retinal degeneration: clinical and molecular aspects and its implications for future therapy

Garcia‑Delgadoetal. Orphanet J Rare Dis (2021) 16:222 https://doi.org/10.1186/s13023‑021‑01843‑z REVIEW Dissecting therole ofEYS inretinal degeneration: clinical andmolecular aspects andits implications forfuture therapy Ana B. Garcia‑Delgado1, Lourdes Valdes‑Sanchez1, Maria Jose Morillo‑Sanchez2, Beatriz Ponte‑Zuñiga2,3, Francisco J. Diaz‑Corrales1* and Berta de la Cerda1 Abstract Mutations in the EYS gene are one of the major causes of autosomal recessive retinitis pigmentosa. EYS‑retinopathy presents a severe clinical phenotype, and patients currently have no therapeutic options. The progress in personalised medicine and gene and cell therapies hold promise for treating this degenerative disease. However, lack of under‑ standing and incomplete comprehension of disease’s mechanism and the role of EYS in the healthy retina are critical limitations for the translation of current technical advances into real therapeutic possibilities. This review recapitulates the present knowledge about EYS‑retinopathies, their clinical presentations and proposed genotype–phenotype correlations. Molecular details of the gene and the protein, mainly based on animal model data, are analysed. The proposed cellular localisation and roles of this large multi‑domain protein are detailed. Future therapeutic approaches for EYS‑retinopathies are discussed. Keywords: Retinal dystrophy, EYS, Ciliopathy, Animal models, Advanced therapies © The Author(s) 2021. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http:// creat iveco mmons. org/ licen ses/ by/4. 0/. The Creative Commons Public Domain Dedication waiver (http:// creat iveco mmons. org/ publi cdoma in/ zero/1. 0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. Background Retinitis pigmentosa (RP, OMIM #26800) is the most common form of inherited retinal degeneration (IRD), with an estimated prevalence of 1 per 4,000 people. Although RP is a rare disease, it represents the primary cause of hereditary blindness in adults, affecting more than one million people worldwide [1]. EYS is a major causative gene for autosomal recessive RP (arRP) [2] in all ethnicities. EYS-retinopathy manifests early in life and produces a severe disability, currently without therapeutic options. The study of the disease’s molecular mechanism has been hampered by the lack of a representative animal model for this human IRD. Information on the cellular localisation and molecular features of EYS, obtained from different vertebrate animal models, is summarised in this review to get insight into this protein’s possible roles in the human retina. Gene therapy is emerging as a safe and effective treatment for some types of RP caused by specific genes such as RPE65. Future therapeutic approaches for EYS-retin- opathies are discussed based on this large gene’s limitations and the current advanced therapies state-of-the-art. Main text The Eyes shut homolog (EYS) gene was identified as the causing gene for retinitis pigmentosa 25 (RP25) (OMIM 612424, NM_001142800) in 2008 [2]. The gene is noted as the largest one expressed in the human eye, extending for 2Mb of genomic DNA in chromosome 6 (6q12.1-6q15) [2]. The genetic structure initially described for EYS included 43 exons, coding for a multi-domain protein of 3,145 amino acids with 21N-terminal epithelial growth factor (EGF)-like and 5 C-terminal Laminin (Lam) G Open Access *Correspondence: [email protected] 1 Andalusian Center for Molecular Biology and Regenerative Medicine (CABIMER), Avda. Americo Vespucio 24, 41092 Seville, Spain Full list of author information is available at the end of the article Page 2 of 14 Garcia‑Delgadoetal. Orphanet J Rare Dis (2021) 16:222 domains, interspaced with additional EGF-like domains [2] (Fig.1). The domain organisation of EYS makes it an orthologue of the Eys gene of Drosophila melanogaster, which encodes the Spam protein, expressed in the open rhabdomere eye of a range of insect species [3, 4]. An independent study of the RP25 locus concurrently identified the EYS gene as causative for RP25 [5], describing a slightly different gene structure, with an additional 63bp exon after exon 41, making a total of 3,165 amino acids for the full-length protein. The extra exon is the subject of alternative splicing. A large EYS transcript was identified, with 10,475 nucleotides, including the untranslated 3′ and 5′ regions. Both initial reports found that the new gene was preferentially and abundantly expressed in the human retina, although minor expression was also found in other tissues [2, 5]. Unfortunately for the study of the associated disease, EYS is missing or interrupted in the genome of several lineages, including the most common animal models: mouse, rat and guinea pig [2]. Regarding the protein function, a direct correlation with its ortholog in Drosophila cannot be assumed since rhabdomeres and photoreceptors have very different cellular structures. Additionally, the lack of sequence conservation in some key residues points to functional differences. Some causative mutations localise in the ten C-terminal residues in patients, not conserved with Drosophila but well conserved among vertebrates [5]. Instead, the fly’s gene has a series of conserved sites for glycosylation absent in the human gene. Zebrafish have been used as an alternative vertebrate model to study the role of Eys protein. The fish gene shares a high degree of similarity with the human gene in its structure (Fig.1) and sequence. Although the predicted protein is short, the missing part corresponds to a low-complexity region that is also missing in other vertebrates with a functional Eys protein [6]. Clinical manifestations After identifying the EYS gene, patients presenting retinal dystrophy without a genetic diagnostic were tested for mutations in this gene, revealing it as the major gene for non-syndromic arRP. EYS has been found in all ethnicities studied, with a prevalence ranging from 5 to 33%, depending on the population. It represents 5% of arRP Fig. 1 Human EYS genetic structure and domain composition of the protein predicted from the full‑length transcript compared to Drosophila and zebrafish orthologues. Some conserved posttranslational modification sites are marked Page 3 of 14 Garcia‑Delgadoetal. Orphanet J Rare Dis (2021) 16:222 in the Dutch and Canadian population, from 5 to 16% in Europe and 18–23.5% in the Japanese cohorts, where EYS is the most frequent cause of IRD [7–16]. RP25 is a severe form of arRP with equal prevalence among males and females. Visual acuity loss usually starts in the second or third decade of life, with a frequent early manifestation as night blindness and a progressive visual field constriction. Patients usually preserve central vision until very late in life [14, 17]. In some cases, the initial presentation includes photophobia instead of night blindness [18]. Relatively young RP25 patients often present subcapsular cataracts and benefit from cataract surgery, even with minor opacities [14, 18]. Regarding ophthalmic data, RP25 usually fulfils all the classic RP hallmarks, with fundus images of bone spicule pigmentation, optic disc pallor, retinal vessel attenuation (Fig. 2) and reduced or non-detectable electroretinogram (ERG) response under both scotopic and photopic conditions. In the initial phases of the disease, central retinal layers appear preserved in the optical coherence tomography (OCT). The atrophy observed is restricted to the retinal pigment epithelium (RPE) and the mid and peripheral retina choriocapillaris. As the disease progresses, macular region thinning is apparent. Fundus autofluorescence (FAF) imaging has demonstrated to help determine the disease’s extent and facilitate diagnosis in atypical cases. In early RP25, the peripheral ellipsoid zone (EZ) is less visible, and the edge of EZ can approximate the visual field along with disease progression [17]. The disease’s clinical features correlate with the histological findings in a study of post-mortem eyes [19]. In this report, donors were of advanced age; therefore, observations correspond to advanced RP25: Gliosis and disorganisation of the retinal structure, particularly in the periphery, with very few photoreceptors present, along with some isolated areas of preserved cones and RPE in the perifovea, possibly explaining the remaining central vision, as shown in Fig.2. Opsin pigments were mislocalised in the surviving cone cells, found mainly in the inner segments and cell bodies instead of outer segments (OS) [19]. Cell migration to inner retinal layers, indicative of a degenerative tissue remodelling process, has also been observed in OCT examination of advanced EYS-retinop- athy [14]. Initially, EYS mutations were only associated with RP [5, 14], being the most common type of clinical presentation (90%). However, macular dystrophy and autosomal Fig. 2 Fundus photography (a, b), infrared (IR) (c, d) and optical coherence tomography (OCT) (E, F) of a male patient (age 78) diagnosed with retinitis pigmentosa (RP). Homozygous EYS variant c.5928‑2A>G was detected in this patient using whole‑exome sequencing. The electroretinogram displayed cone and rods extinguished responses. Best‑corrected visual acuity (BCVA) OD + 1 logMAR and OS hand motion at 1 m. Biomicroscopy of anterior pole: OU pseudophakia. Fundus photography shows a typical RP phenotype (a, b). The optic disk appears pale, vessels are very thin, and there is extensive atrophy of the retinal pigment epithelium and choriocapillaris with bone spicule pigmentations. Preservation of central retinal islet with a perifoveal orange halo. a, b The IR image shows the retinal islet’s detail and the scan lines where the OCT was performed (c, d). OCT scans display the bilateral perifoveal retinal islet. The ellipsoid zone is preserved and limits the retinal islet (e, f; arrows) Page 4 of 14 Garcia‑Delgadoetal. Orphanet J Rare Dis (2021) 16:222 recessive cone-rod dystrophy (arCRD) are other possible manifestations of EYS-retinopathy [16, 20–22]. EYS- arCRD has been reported with a low frequency (1%) [22], manifesting with a loss in central vision, predominant degeneration of the macular region and decreased amplitudes in the cone and rod ERG waves [20]. EYS-arCRD has been described in a patient with the same compound heterozygous EYS mutations [22] that cause arRP in other cases, implying the existence of unknown factors that modify the clinical phenotype. There is not enough genetic data to determine the prevalence of EYS mutations among CRD patients [23]. However, it is relevant to note that the retinal degeneration pattern in eys knockout zebrafish, the most used vertebrate model for EYS- retinopathy, is similar to CRD [24]. Genotype–phenotype correlation The array of disease-associated mutations reported for EYS includes insertion, deletion, nonsense or missense substitution and splice site mutation, with variable representation in different cohorts [2, 5, 8, 9, 14, 18, 25, 26]. The most common mutations in EYS are truncating mutations that lead to premature stop codons, removing LamG or EGF-domains [13], including frameshift and nonsense mutations. Missense mutations have also been described and are usually found in combination with a truncating mutation [8, 9, 14, 18, 25, 27]. Additionally, midsized genomic rearrangements cause 4% of EYS-arRP and participate as the second pathogenic variation in 15% of cases [28]. Compound heterozygous inheritance of two different copy-number variation (CNV), or a CNV and a nonsense mutation in EYS, have also been described [9, 29, 30]. Several authors have tried to link the type of mutation with the clinical presentation, but different trends have been found depending on the cohort studied. Iwanami and cols. [13] associated truncating mutations to a severe decline in visual acuity. The explanation would include the nonsense-mediated decay (NMD) of the truncated transcripts, leading to decreased EYS protein dose. McGuigan and cols. [26] also proposed NMD, based on the relatively uniform location of truncating mutations along the gene sequence and the observation of milder cases associated with truncating mutations that affect the last C-terminal EGF and LamG domains. These authors proposed that the mutations would result in hypomorphic alleles, in which mRNA may avoid NMD, producing a truncated EYS protein with some residual functionality. In another cohort, studied by Bonhilla and cols. [19], midsize exonic deletion correlated with better preservation of macular cones and central vision than truncating mutations. Regarding missense mutations, they can be found as compound heterozygote with another missense mutation or a truncating mutation. It is currently under debate if missense changes produce a less severe disease phenotype than truncating mutations. Contradictory data from different cohorts keep this question open. Moreover, the effect of missense mutations could be influenced by additional single nucleotide polymorphisms (SNPs) in the EYS gene or interaction with other modifier factors in the genetic background that might affect the phenotype. The pathogenicity of many missense changes remains unclear, even for conserved residues [31]. Regarding the gene sections affected by the mutation, it has been reported a higher frequency of diseaseassociated mutations close to the C-terminus [5, 9, 11]. These observations and the fact that some C-terminal domains are highly conserved support the EYS C-ter- minal region’s importance for protein functionality. On the contrary, Ogino and cols. [17] suggested that variants near the distal portion of the protein will have a minor effect on the protein function, only impairing EYS binding with its interactome. In a report covering more than 200 EYS mutations [26], a homogeneous distribution of mutations along the gene sequence was described, with a uniform spread of splice site and truncating mutations. Differences were found in missense mutations, more abundant in the C-termi- nal region, and in deletions, mainly found in the first half of the protein. The significance of this data is still unclear since many deletions also result in premature stop codons. The type of mutation cannot be easily related to the phenotype’s severity, as some patients with a relatively mild disease harbour truncating mutations. In contrast, others with missense mutations present a severe disease [32]. In the study of Sengillo and cols. [16] patients were classified regarding fundus FAF: a crescent-shaped autofluorescent ring was associated with C-terminal mutations whilst the typical autofluorescent ring in the distal area, characteristic of RP patients, was found in patients with N-terminal mutations. Moreover, phenotypic variability among patients with the same mutations has also been shown [5, 32], indicating the input of other contributing factors to the clinical presentation and preventing the use of the genetic diagnostic to predict the disease’s evolution and severity. Moreover, all EYS patients preserve a normal visual acuity until their second decade of life means that EYS protein is not essential in retinal development. Some unknown factor may compensate for the EYS defect, allowing for visual function in the first decades of life. It has been already mentioned that the EYS gene is lost in several species, in which its function has to be played or compensated by other factors. The possible role of Page 5 of 14 Garcia‑Delgadoetal. Orphanet J Rare Dis (2021) 16:222 additional genetic modifiers adds a layer of complexity to the understanding of genetic implications on the disease’s prognosis. Another significant gap in current knowledge that impairs the prediction of the mutations’ effect is the incomplete understanding of EYS function in the healthy retina, preventing the prediction of the possible effect of mutations in conserved residues or those affecting functional domains. To better understand EYS-retinopathies’ pathophysiology, it is essential to perform functional studies that focus on the effect of mutations on the different EYS isoforms and their impact on the retina. In a cellular modelling study [33], photoreceptor–directed fibroblasts from EYS-RP patients were used to evaluate the effect of different mutations on EYS transcripts, finding that level of NMD depends on the specific mutation. In summary, the variability in the severity of missense mutations and the lack of hotspots in EYS make genotype–phenotype relationships challenging to predict. Being EYS, a gene of high prevalence in IRD, the analysis of larger cohorts comprising a wide array of mutation types and longitudinal studies on the natural course of the disease would add vital information to predict the clinical evolution and prognosis of genetically diagnosed patients. Molecular aspects Genomic and protein databases predictions based on EYS gene structure [2, 5] depict a full-length protein structure divided into two distinct halves: a N-terminal part having a signal peptide followed by a stretch of EGF-like domains and a C-terminal part rich in LamG domains interspaced with additional EGF-like domains (Fig. 1). Proteome dynamic regulation via splicing is conserved in vertebrate neurons and contributes to the nervous system’s complexity [34]. Concerning EYS, a growing number of variant transcripts have been identified, resulting from alternative splicing [35, 36]. Expression of different isoforms has been detected in the retina and other tissues. The diverse EYS isoforms, with particular domain composition and structure, will perform specific roles depending on time, cellular compartment or tissue, complicating the analysis of the effect of mutations. Isoforms expressed in the human retina and their main characteristics can be found in Table1. The longer isoforms 1 and 4 only differ in the insertion of one exon between exons 41 and 42. High expression of these longer isoforms was found in the retina in the initial descriptions of the EYS gene [2, 5]. Isoforms 2 and 3 correspond to the 5′ part of the gene, comprising the signal peptide and five EGF-like domains, with some differences in their C-terminal section’s length and sequence. Isoforms 2 and 3 are expressed in the retina and testis [35]. All the retinal transcripts known for EYS enclose the signal peptide and longer or shorter stretches of the 5′sequence of the gene. Transcripts containing the 5′ segment of the gene are conserved among distant vertebrate species [35, 36]. A fifth transcript, including only 3′ sequences, starting from exon 37 and containing two LamG domains and EGF-like domains, was recently identified in human dermal fibroblasts [36]. This transcript without signal peptide presents some variation due to splicing, generating isoforms 5–1, 5–2 and 5–3. These isoforms are predicted to be expressed ubiquitously, mainly in hepatocyte, bile duct, prostate, myoblast, lung, kidney and intestinal epithelial cells [36]. Table 1 EYS isoforms expressed in the human retina. Page 6 of 14 Garcia‑Delgadoetal. Orphanet J Rare Dis (2021) 16:222 The two distinct halves of the full-length EYS protein will likely have different roles and interactors. Shorter isoforms with just the EGF-rich or the LamG-rich sections will probably have particular localisations and functions, which will be relevant for analysing and predicting the phenotypic impact of genetic variants. Functions ofEYS andpossible mechanisms ofthedisease a. EYS localisation and ciliary role Most of the knowledge about this gene comes from its ortholog in Drosophila (eys gene; eyes shut protein), an extracellular protein essential to maintaining the inter-rhabdomeric space [37]. It has also been localised to the extracellular space of the fly’s mechanosensory neurons, supporting the sensory cell [3]. Although the two orthologs share structural similarities, some molecular differences will affect posttranslational modifications such as glycosylation, impacting protein localisation and function. Together with the critical structural differences between the fly and vertebrate eyes, these facts limit the utility of the information on localisation, interactions, and function of eys to understand human EYS role. Prominin is a highly glycosylated transmembrane protein known to localise in membrane protrusions of many cells. In the retina, it is found in the membranous protrusions of the OS base, which in zebrafish and human are organised as a ring of calyceal processes. Mutations in PROM1 cause arRP and macular degeneration [38–40], and its function has been described as essential for membrane structure and disc morphogenesis. Prominin interacts with actin filaments and protocadherin21, also localised to the OS bottom [40]. It has been shown [41] that the interaction between Prominin and Eys is genetically conserved between Drosophila and human. Human PROM and EYS were able to replace the fly’s mutant proteins, rescuing the morphology of the rhabdomere [41], suggesting that the interaction between these two partners has been evolutionarily conserved and, thus, may still be playing a role in vertebrates. The localisation of the full-length Eys protein was first reported in the OS of photoreceptors in pig retinal Sects.[25] and further refined to the proximity of the ciliary axoneme of rod and cones. Another study reported Eys’ localisation in the cytoplasm of ganglion cells in macaque retinas [35]. Further details were provided in a concurrent study [42] in which some differences in cellular localisation of Eys were found between different vertebrate retinas. In zebrafish, Eys was found in the connecting cilium/ transition zone area. In macaque retinas, most of Eys labelling was found in the interphotoreceptor matrix (IPM) surrounding cone OS and stained with less intensity the OS of rods and the region between OS and RPE. In both photoreceptor types, Eys localised in the proximity of the connecting cilium/transition zone. Although the most frequent form of EYS-retin- opathy is rod dystrophy, it has been shown that cones also express this protein, which might account for EYS-arCRD cases. Even with the interspecific variability described, the value of zebrafish as a model for the study of EYS is apparent. Knocking eys induces retinal degeneration in the fish [6, 42]. A detailed description of the morphology of mutant photoreceptors by electron microscopy showed the collapse of the ciliary pocket, formed by a plasma membrane invagination that separates the outer and inner segments. As expected from its sequence, Eys was localised as an extracellular protein in the IPM. Functionally, Eys demonstrated to be essential for the structural maintenance of the ciliary pocket. Another study in zebrafish reported visual impairment when eys was mutated, along with mislocalisation of proteins of the OS of the photoreceptors and distortion of F-actin filaments, mainly affecting cones [24]. Considering that actin filaments are essential for protein transport, this might explain the mislocalisation of OS proteins. It is to note that eys zebrafish mutants present a disruption in their calyceal processes. These cellular structures are actin-filled microvilli anchored to the inner segment by F-actin roots and superficially encircling the OS base. Although their function has not been determined, it has been proposed that these microvilli provide mechanical strength to the base of the OS, a part of the photoreceptor cell subjected to physical stress due to the continuous synthesis of new discs. The calyceal processes have been described in photoreceptors of zebrafish, frogs, pig and primates, including human, but are absent in mouse retinas [43]. The presence of calyceal processes curiously coincides with eys gene distribution among these vertebrate species. In a parallel case, USH1 proteins, including Cadherin-23, localise to the calyceal processes, which in macaques and Xenopus present F-actin roots. Mouse and rat animal models, devoid of calyceal processes and F-actin roots in the OS Page 7 of 14 Garcia‑Delgadoetal. Orphanet J Rare Dis (2021) 16:222 base, do not phenocopy the retinal features of USH1 mutations. The absence of calyceal microvilli structures in mouse and rat and the fact that they become disorganised in the standard tissue fixing conditions has undermined these structures’ study. However, it might be worth focusing on the interactions between F-actin roots of calyceal processes, its associated proteins such as Protocadherin23, the transmembrane Prominin and the large protein associated with the IPM Eys in the maintenance of the membranous structures of the transition zone of vertebrate photoreceptors. Considering what is known for Drosophila, where mutations in the eys gene collapse the matrix-filled inter-rhab- domeric space, the finding of Eys defects as causative for the vertebrate’s shrink ciliary pocket suggests further functional homologies between the fly and the vertebrate proteins. These similarities might be extended to EYS interaction with PROM1. A hypothetic network of proteins comprising EYS, PROM1 and ACTIN can be proposed to be involved in the structural maintenance of the photoreceptors’ transition zone (Fig.3). Prominin is known to be involved in the structural organisation of cellular protrusions, interacting with F-actin filaments and cadherins and has been localised to the OS base. Although PROM1 mutations cause retinopathy, the role of this protein in photoreceptors is poorly studied [44]. Summing up from the currently available data, the EYS function is essential in the structural organisation of the connecting cilium of vertebrate photoreceptors. Approximately 25% of all IRDs can be categorised as ciliopathies [45], but EYS is the first extracellular protein known to cause ciliopathy. Even so, it cannot be ruled out for some EYS isoforms to have additional extracellular roles in the conformation of the IPM that fills the space between photoreceptors and between them and RPE. b. LG domains of EYS and the interaction with the IPM The IPM is mainly composed of glycoproteins and proteoglycans and has an essential function in the structural maintenance of tissue, in the transport and recycling of cellular components, and in the maintenance of photoreceptor differentiation state and survival. EYS is one of several non-syndromic RP causing genes that encode a protein that binds hyaluronic acid and localises in the IPM. The EYS protein contains LG domains that make it a candidate to bind glycosaminoglycan chains, and some of its possible roles may be mediated through interactions with matriglycans. Matriglycan is a linear chain of repeating disaccharides found in dystroglycan (DG) in the cell surface. DG is formed by extracellular α-DG and transmembrane α-DG that interacts with the cytoskeleton. Agrin, laminin, perlecan, neurexin and pikachurin Fig. 3 Possible localisation and interactions of EYS in the transition zone of photoreceptors. The extracellular protein is found in the IPM close to the primary cilium and the OS. A proposed localisation in the ciliary pocket and an interaction with Prom1 in the calyceal processes are shown Page 8 of 14 Garcia‑Delgadoetal. Orphanet J Rare Dis (2021) 16:222 are extracellular α-DG-interacting proteins through their LamG domains [46–49]. Pikachurin, specifically, is essential to maintain the photoreceptor ribbon synapsis [49]. It has been proposed that EYS could interact with matriglycan through its LamG domains [50]. In zebrafish, it has been demonstrated that EYS binds the O-mannosyl-glycan matriglycan [50]. A reduction in the level of matriglycans through a mutation in Pomgnt1, the O-mannose β1,2N-acetylglucosa- minyltransferase 1, results in EYS mislocalisation from the connecting cilium area to synaptotagmine-1 positive secretory vesicles. The phenotype of these mutant fishes includes retinal degeneration with ageing. In humans, hypomorphic mutations in POMT- GnT1 cause RP76 [51, 52]. The clinical manifestation of a dysfunctional POMGTn1, leading to retinal dystrophy, might be mediated by a defective interaction between EYS and the extracellular matrix. A graphic representation of this possible interaction is shown in Fig.4. Although many mouse models with different matriglycan-related mutations phenotypically present retinal defects [49, 53–57], the Pomgnt1 mutation in mouse does not produce an RP76-like phenotype like in zebrafish, pointing to an effect mediated by EYS [50]. It is yet to be established whether another matriglycan-binding protein plays the function of EYS in mouse, or if mouse photoreceptors have some structural adaptation to compensate for Eys’ loss. c. EGF-like domains of EYS and Notch signalling EGF-like domains contain 30 to 40 amino acids with sequence similarity to the EGF protein and, structurally, present three internal disulfide bonds. These domains are usually found as tandem repeats in secreted proteins or the extracellular domains of transmembrane proteins and are involved in protein–protein interactions [58]. The EGF-repeats participate in Notch signalling, a conserved signalling pathway essential for animals’ development and health [59]. In mammals, Notch receptors have up to 36 EGF-repeats with diverse functional roles in protein folding, trafficking or interaction between Notch ligands and receptors [60, 61]. Structural similarity of EYS-EGF domains with Notch 1 has been proposed to be related to a functional role of EYS in Notch signalling in muscle regeneration [62] and possibly to other human diseases. Most Notch EGF-repeats have O-glycosylation sites, whose defects have been associated with human diseases [59, 63]. The effect of EGF O-glycosylation in Notch and other EGF-rich proteins has been mainly studied in Drosophila. Two proteins with multiple EGF O-glycosyla- tion sites involved in retinal disease are Crumbs and Eys [64]. Both proteins are part of a genetic network that determines the apical part of the photoreceptor’s development and maintenance in the fly [37]. Loss of O-glycosylation in Eys impairs its extracellular secretion and, consequently, the rhabdomere separation [64]. The enzyme O-glucosyltransferase 1 is essential for Eys’ correct folding and its secretion to the extracellular space [64]. Knowing that sugars are only added to properly folded EGF-domains [65], it has been suggested that the O-glycosylation of EGF- domains of Eys might work as quality control and serve to stabilise the folded structure [60]. The sensitivity of Notch, Crumbs and Eys to defects in EGF O-glycosylation in Drosophila is very different. Notch signalling and Eys function are affected in a similar way, showing a temperature-dependent phenotype indicative of protein misfolding, while Crumbs’ trafficking is affected but not its function. Eys and Crumbs biosynthetic traffic share common factors in the fly [66]. Human EYS also harbours multiple O-glycosylation target sites, with 4–5 of them clustered in a similar way to the fly Eys, suggesting that the O-glycosylation regulatory role in this protein might be conserved [64]. In humans, CRB1 and CRB2 contain 13 and 8 O-glycosylation sites, respectively (Fig. 5) [64], and mutations produce RP12 [67] and other retinal dystrophies. Their role is not entirely understood, but CRB proteins are involved in the scaffolding of cell-to-cell adhesion and the structural maintenance of the photoreceptor layer. The lack of a murine model for RP25 prevents the complete mechanistic interpretation of the data Fig. 4 Graphic representation of the proposed interaction between EYS and the ECM components Page 9 of 14 Garcia‑Delgadoetal. Orphanet J Rare Dis (2021) 16:222 obtained in Drosophila and zebrafish. The use of patient-derived cellular models and the organoid models of retinal disease are promising tools to advance the understanding of EYS-associated diseases’ molecular pathophysiology. d. Roles of EYS outside the retina EYS gene, as described in the literature, is mainly expressed in the retina, but it has also been identified in muscle, spinal cord, brain [62], fat, colon, heart [68], and testis [35]. Specific gene products of EYS, generated by alternative splicing, maybe playing different roles in different tissues. A genome-wide association study (GWAS) designed to identify genetic risk factors for severe myopathic conditions caused by statin treatment identified three EYS SNPs in intron 26, near the first LamG domain [62]. Statin is a common drug used to control cholesterol blood levels. Although side effects affecting muscle are not rare, a minor fraction of patients develop severe neuromuscular disorders coincident with statin treatment. The authors identified several different EYS gene products expressed in the human brain, skeletal muscle and spinal cord in addition to the known retinal transcripts [62]. These results suggested that EYS could intervene in protecting motor neurons and skeletal muscle cells from exercise-induced damage. Isackson and cols. [62] determined that the risk was linked to only one copy of the variant allele, but the effect of the variant in the protein was not studied as no molecular dissection of the EYS isoforms expressed in the affected muscle patients were performed in the study. It is known that Eys protein in Drosophila plays a role in protecting mechanoreceptor and chemoreceptor organs from hyperosmotic shock by providing stiffness and maintaining cellular integrity and tissue morphogenesis [69]. In humans, it has been proposed that EYS may also protect muscle cells and motor neurons from hyperosmotic damage, which is one of the possible mechanisms of exercise intolerance and statin-induced myopathy [62]. Analysing protein domains to hypothesise a possible mechanistic implication for EYS in muscle, these authors suggested that the N-terminal EGF-domains resemble the structure of Notch1. It has been demonstrated that proteins with these domains bind together, making EYS a candidate to participate in Notch signalling, resulting in developmental defects and several human diseases. Notch signalling is involved in the regeneration of muscle tissue after exercise via satellite-cell differentiation Fig. 5 O‑glycosylation sites in human EYS, CRB1 and CRB2 proteins