GEMIN5 gene (known as GEM-ASSOCIATED PROTEIN 5 in Online Mendelian Inheritance in Man [OMIM], MIM#607005), mapped to 5q33.2, encodes gem nuclear organelle–associated protein 5 (GEMIN5) (Gubitz et al., 2002). GEMIN5 is a WD repeat protein and a component of the survival of motor neurons (SMN) complex. GEMIN5 contains different structural domains, including the WD40 repeat domain located at the N-terminal region (1-739AA), a tetratricopeptide repeat (TPR)-like dimerization domain with 17 helices (845-1097AA), and a bipartite non-conventional RNA-binding site (designated as RBS1 and RBS2, 1287-1508AA) (Embarc-Buh et al., 2021; Jin et al., 2016; Moreno-Morcillo et al., 2020). GEMIN5 is involved in the spliceosomal small nuclear ribonucleoprotein biogenesis (Francisco-Velilla et al., 2022), acting as a signal recognition particle-interacting protein (Piazzon et al., 2013), ribosome interacting factor (Francisco-Velilla et al., 2016), and mRNA translation regulator (Martinez-Salas et al., 2020). WD40 repeat domain is involved in the recognition of snRNAs (Francisco-Velilla et al., 2022). TRP-like domain with 17 helices that oligomerizes as a canoe-shaped homodimer is vital for protein architecture and activity (Ibrahim et al., 2023). RBS1–RBS2 exerts multiple cellular functions such as RNA-binding specificity and affinity, as well as translation repression and control of the protein stability (Embarc-Buh et al., 2021; Jin et al., 2016; Moreno-Morcillo et al., 2020).
Clinically, variants in GEMIN5 have been associated with neurodevelopmental disorder with cerebellar atrophy and motor dysfunction (NEDCAM) syndrome (OMIM#619333) (Ibrahim et al., 2023), neurodevelopmental disorder characterized by cerebellar atrophy, developmental and cognitive delay, ataxia, motor dysfunction, and hypotonia. The association between GEMIN5 variants and epilepsy has not been fully understood and given enough attention. Here, we reported two patients harboring biallelic variants in the GEMIN5 gene and suffering from early-infantile developmental and epileptic encephalopathies (EIDEE) (Zuberi et al., 2022), but otherwise presenting with clinical features distinct from NEDCAM syndrome, broadening the phenotypic spectrum of GEMIN5. We also analyzed all 48 patients with GEMIN5 variants, focusing on the correlations between epilepsy and molecular sub-regional locations.
MATERIALS AND METHODS SubjectsPatients with unexplained EIDEE were recruited from the First Medical Center of Chinese PLA General Hospital between July 2020 and May 2023. Written informed consent was obtained from the patients and their parents. The project was approved by the Ethical Committee of the Chinese PLA General Hospital. All the study procedures were performed in accordance with the Declaration of Helsinki. Detailed clinical information was collected, such as age, gender, seizure types and frequencies, general and neurological examination results, family history, responses to anti-seizure medicines (ASMs), results of video-electroencephalography (VEEG), and cranial magnetic resonance imaging (MRI). EIDEE or epilepsies were diagnosed according to the criteria of the Commission on Classification and Terminology of the ILAE (Zuberi et al., 2022). EIDEE includes Ohtahara syndrome and early myoclonic encephalopathy, previously categorized as neonatal and infantile epileptic syndrome (Lombroso, 1990; Yelin et al., 1999). EIDEE is a syndrome characterized by seizures in the first 3 months of life, frequent seizures, drug resistance, and developmental delay. Patients have abnormal interictal electroencephalograms that may include suppression-bursts (SBs), diffuse slow waves, or multifocal discharges (Ohtahara & Yamatogi, 2006). Neuroimaging, metabolic, and genetic testing provide a precise etiologic diagnosis in approximately 80% of patients (Bayat et al., 2021).
Trio-based whole-exome sequencing (WES)Venous blood was taken from consenting patients and their parents by EDTA anticoagulant tube. Then genomic DNA was extracted from venous blood samples using a RelaxGene Blood DNA system (Tiangen Biotech Co., Ltd.). Then the libraries for whole-exome sequencing were constructed with NanoPrep DNA Library Preparation Module (for MGI), 96 rxn. The libraries were then sequenced on a BGI MGISEQ-2000 sequencer. After obtaining the raw reads, read alignment was performed using the Burrows-Wheeler Aligner tool (version 0.7.17) with default parameters against the human genome assembly hg19 (GRCh37) as previously described (Li & Durbin, 2010). The generated bam file was then sorted and deduplicated by SAMtools (Li et al., 2009) and Picard, respectively. Then Genome Analysis Toolkit (GATK;
We aimed to evaluate the relationship between the genotype and phenotype through exhaustively searching GEMIN5 pathogenic variants on PubMed up until May 2023 to identify studies published in English using the following terms: GEMIN5, epilepsy, seizure, EIDEE, and NEDCAM syndrome. All pathogenic variants in patients with neurological phenotypes were included and analyzed. We performed molecular modeling analysis of the variants in protein structure. Pymol was used for protein structure mapping. The species conservation analysis of GEMIN5 protein has been conducted.
RESULTS Identification of GEMIN5 variantsTwo patients with biallelic truncating and missense variants in GEMIN5 were identified (Hg19, chr5:154282663T > A: NM_015465: c.2705T > A: p.(Leu902Gln) and Hg19, chr5:154299603-154299603delTinsAGA: NM_015465: c.1523delTinsAGA: p.(Leu508*) for patient 1; Hg19, chr5:154281002C > G: NM_015465: c.2911C > G: p.(Gln971Glu) and Hg19, chr5:154284147-154284148delCT: NM_015465: c.2551_c.2552delCT: p.(Leu851fs*30) for patient 2) (Table 1; Figure 1a,b). Two patients had no other pathogenic or likely pathogenic variants. Variants of GEMIN5 were annotated based on transcript NM_015465, and the missense variants of two patients were confirmed by Sanger sequencing.
TABLE 1 Epileptic patients with gem nuclear organelle–associated protein 5 (GEMIN5) variants.
Abbreviations: ASM, anti-seizure medicine; CLB, clobazam; DEEs, developmental and epileptic encephalopathies; EEG, electroencephalography; EIDEE, early-infantile developmental and epileptic encephalopathies; GTCS, generalized tonic–clonic seizure; LEV, levetiracetam; LGT, lamotrigine; MRI, magnetic resonance imaging; NA, not applicable; PB, phenobarbital; SBs, suppression-bursts; SeLECTS, self-limited childhood epilepsy with centrotemporal spikes; TPM, topiramate; VGB, vigabatrin; VPA, sodium valproate; ZNS, zonisamide.
FIGURE 1. Genetic data on the patients with gem nuclear organelle–associated protein 5 (GEMIN5) variants. (a and b) Pedigree of the two families. The black arrow points to the probands. (c and d) The variant amino acids in our patients were conserved from multiple species.
The amino acid residues of the two missense variants are highly conserved in various species (Figure 1c,d). The two missense variants were suggested to be damaging or probably damaging by four tools (Table 2). The pathogenicity of p.Leu902Gln and p.Gln971Glu was predicted as uncertain, whereas p. Leu508* and p. Leu851fs*30 were predicted as likely pathogenic, according to ACMG code-level (Table 2).
TABLE 2 Genetic features of the individuals with gem nuclear organelle–associated protein 5 (GEMIN5) variants.
Patients | cDNA change/Protein alteration/Transcripts | MAF | Variant class | Inheritance | ACMG code-level | SIFT |
Polyphen2 HDIV Pred |
Polyphen2 HVAR Pred |
Mutation Taster Pred |
1 | Hg19, chr5:154282663T > A: NM_015465: c.2705T > A: p.(Leu902Gln) | – | Missense mutation | Maternal |
Uncertain PM2+PM3_ Supporting |
D (0) | PD (0.986) | PD (0.965) | D (Gubitz et al., 2002) |
Hg19, chr5:154299603-154299603delTinsAGA: NM_015465: c.1523delTinsAGA: p.(Leu508*) |
– | Nonsense mutation | paternal |
Likely pathogenic PVS1+PM2_ Supporting |
– | – | – | – | |
2 | Hg19, chr5:154281002C > G: NM_015465: c.2911C > G: p.(Gln971Glu) | – |
Missense mutation |
paternal |
Uncertain PM2+PM3+PP3_ Supporting |
D (0.005) | PD (Gubitz et al., 2002) | PD (0.998) | D (0.991089) |
Hg19, chr5:154284147-154284148delCT: NM_015465: c.2551_c.2552delCT: p.(Leu851fs*30) |
– | frameshift variant | maternal |
Likely pathogenic PVS1+PM2_ Supporting |
– | – | – | – |
Abbreviations: D, damaging; MAF, minor allele frequency from Genome Aggregation Database; NA, not applicable; PD, probably damaging; PM2_Supporting, absent from controls in Exome Sequencing Project, 1000 Genomes Project, or Exome Aggregation Consortium; PM3_Supporting, for recessive disorders, detected in trans with a pathogenic variant; PP3_Supporting, multiple lines of computational evidence support a deleterious effect on the gene or gene product; PVS1_Supporting, the mutation causes changes in protein function.
Clinical informationThe main clinical features of the two patients are summarized in Table 1. Two patients were both born to non-consanguineous parents.
Patient 1, a 20-month-old girl, is the first child of healthy parents without any family history of intellectual disability (ID) or epilepsy (Figure 1a). She was delivered by full-term cesarean section after an uneventful pregnancy. The patient experienced focal motor seizure 20 days after birth. The seizure types later changed to clusters of epileptic spasms and generalized tonic–clonic seizures (GTCSs). Neurological examination revealed hypotonia. VEEG showed SBs at approximately 1 month old (Figure 2a). Cranial MRI suggests dysgenesis of the corpus callosum and cerebellar hypoplasia at approximately 6 months old (Figure 2c). Blood amino acid and urinary organic acid screening results did not show significant abnormalities. She was treated sequentially with corticotropin (ACTH), oral glucocorticoids, sodium valproate (VPA), topiramate (TPM), levetiracetam (LEV), vigabatrin (VGB), phenobarbital (PB), ketogenic diet, lamotrigine (LGT), clobazam (CLB), and zonisamide (ZNS), but the seizures were not effectively controlled at 6 months old (Table 1). Subsequently, a diagnosis of EIDEE was made based on her clinical and EEG features. Her psychomotor development was behind that of healthy children of the same age at 6 months old, and she did not exhibit vocalizations or cooing, hold her head up, or follow voice and vision. Through telephone follow-up, patient 1 experienced multiple isolated epileptic spasms daily at 20 months old. Patient 1 still lacks head control, rolling over, sitting independently, or vocalization. Patient 1 is currently taking CLB and ZNS, with caregivers reporting a relatively positive response to CLB. No follow-up MRI was conducted post-discharge, and the repeat VEEG showed similar findings as before.
FIGURE 2. Electroencephalogram (EEG) and neuroimaging results of the patients with gem nuclear organelle–associated protein 5 (GEMIN5) variants. (a) Patient 1, female, approximately 1 month old. EEG during awake without anti-seizure medicine (ASM) (bipolar longitudinal montage. Sensitivity 100 uV/cm, high-pass filter 1 Hz, low-pass filter 70 Hz): There are suppression-bursts (SBs). (b) Patient 2, female, approximately 6 months old. EEG during awakeness with the use of levetiracetam (LEV), topiramate (TPM), vigabatrin (VGB), and clobazam (CLB) (average montage. Sensitivity 150 uV/cm, high pass filter 1 Hz, low pass filter 70 Hz): There are SBs. (c) Cranial magnetic resonance imaging (MRI) of patient 1 (approximately 6 months old) showed dysgenesis of the corpus callosum and cerebellar hypoplasia in sagittal T1. (d) Cranial MRI of patient 2 (approximately 6 months old) showed dysgenesis of the corpus callosum and cerebellar hypoplasia in sagittal T2.
Patient 2, a 17-month-old girl, is the first child of unrelated, healthy parents without any family history of ID or epilepsy (Figure 1b). Her mother was diagnosed with hypertension 3 days before delivery, but the details were not known. Patient 2 was delivered at 36 + 5 weeks with meconium-stained amniotic fluid, a knotted umbilical cord, and no hypoxic asphyxia at birth. She developed tonic seizures with no obvious cause 1 week after birth. She had experienced GTCS 1 month later, which lasted for about 2 min and then resolved on its own. The seizure types later changed to clusters of epileptic spasm. Neurological examination revealed hypertonia. She also has congenital chondrodysplasia of the larynx, congenital clubfoot on the right side, and bilateral hip dislocation. VEEG during the interictal period showed SBs at approximately 6 months old (Figure 2b). Cranial MRI suggests dysgenesis of the corpus callosum and cerebellar hypoplasia at approximately 6 months old (Figure 2d). She was treated sequentially with ACTH, oral glucocorticoids, TPM, VPA, ZNS, CLB, and VGB, and the seizures were not effectively controlled (Table 1). Her growth and development were behind that of healthy children of the same age at 6 months old, and she did not exhibit vocalizations or cooing, hold her head up, or follow voice and vision. Through telephone follow-up, patient 2 experienced four to five episodes of spasms in the upper limbs per day at 17 months old, with spontaneous recovery within a few seconds. Patient 2 can maintain head control for approximately 5 min, cannot sit independently or roll over, but is able to vocalize unconsciously. The patient is currently taking VPA, LGT, and CLB, with caregivers reporting the best seizure control with CLB. No follow-up MRI was conducted post-discharge, and the repeat VEEG showed similar findings as before.
Structure alteration of GEMIN5 proteinAs shown in Figure 3, GEMIN5 contains the WD40 repeat domain, TPR-like domain, RBS1, and RBS2. Structural model of GEMIN5 indicated variants p.Leu902Gln, p.Gln971Glu, and p.Leu851fs*30 were located within the TPR domain, and variant p.Leu508* was located in the WD40 repeat domain. Both missense variants changed the hydrogen bonds (Figure 4a–d).
FIGURE 3. Schematic diagram of gem nuclear organelle–associated protein 5 (GEMIN5) and the localization of the variants of GEMIN5 identified in previous reports (variants that cause epilepsy are highlighted in red and variants that do not cause epilepsy are highlighted in black) and in our study (highlighted in blue). The number represents the number of patients with this mutation.
FIGURE 4. Changes in gem nuclear organelle–associated protein 5 (GEMIN5) structure. (a and b) The protein changes of Leu902Gln. (c and d) The protein changes of Gln971Glu. In (a) and (c), white represents carbon atoms, red represents oxygen atoms, yellow represents sulfur atoms, blue represents nitrogen atoms, and the green dotted lines represent hydrogen bonds.
In the PDB database, the structure of the GEMIN5 protein has been fully resolved, and the complete amino acid sequence of the protein can be obtained. According to the prediction results, p.Leu902Gln results in the substitution of leucine (Leu) with glutamine (Gln). Figure 4a,b illustrates the impact of the Leu902Gln mutation on the structure and interactions with other amino acids. In the wild-type protein, L902 forms hydrogen bonds with Y903 and R904. After the mutation, in addition to the two original hydrogen bonds, Q902 also forms hydrogen bonds with D898 and I906, respectively. Compared to the wild-type protein, although the mutant protein shows a significantly increased number of hydrogen bonds, there is no apparent effect on the three-dimensional structure. However, further experimental verification is required to determine whether this variant will alter the protein's activity.
The p.Gln971Glu results in the substitution of glutamine (Gln) with glutamic acid (Glu) in the amino acid sequence. Figure 4c,d illustrates the impact of the Gln971Glu mutation on the protein structure and interactions with other amino acids. In the wild-type protein, Q971 forms hydrogen bonds with F968 and L972, respectively. After the mutation, in addition to the original two hydrogen bonds, E971 also forms a hydrogen bond with Q975. The mutant protein exhibits additional hydrogen bond formations compared to the wild-type. The variation at this position can be clearly observed in the three-dimensional structural prediction of the protein, affecting the original arrangement of some protein main chains and consequently altering the folding structure of certain protein regions.
Genotype-phenotype correlation of GEMIN5 variantsWe analyzed the genotype-phenotype relationship in all reported GEMIN5 pathogenic variants with detailed clinical phenotypes. Previously, 45 kinds of GEMIN5 variants in 48 patients have been reported in 5 published papers (Francisco-Velilla et al., 2022; Ibrahim et al., 2023; Kour et al., 2021; Rajan et al., 2022; Saida et al., 2021). Including our 2 patients, a total of 49 variants in 50 patients were collected and analyzed. Clinical and molecular details of patients with epilepsy are listed in Table 1, and patients without epilepsy are listed in Table S1. Ten out of the 50 patients had epilepsy. Table 1 presents the genetic origin of each mutation site. We further analyzed the sub-regional locations and found that half of those variants in 10 patients with epilepsy were located in the TPR-like domain. The frequency of missense mutation is the highest. Two hotspot/recurrent variants, including p.Leu1367Pro (3 patients with epilepsy), located in RBS1, and p.lle988Phe (2 patients with epilepsy), located in TPR-like domain, were observed (Tables 1 and 3). Seven of 10 patients presented with epilepsy within the first year of life, but detailed manifestations of seizures were not reported. Four patients were reported with a history of ASMs. Among them, our two patients with EIDEE had drug resistant epilepsy and still presented with seizures, whereas the other two were well controlled by CLB and LEV, respectively. All 10 patients with epilepsy had development delays (Table 1).
TABLE 3 Hotspot/recurrent variants of gem nuclear organelle–associated protein 5 (GEMIN5) gene.
Domain | Hotspot/Recurrent variants | Number of patients |
Epilepsy Yes or No |
WD40 repeat domain | p.Ser543Gly | 2 | No |
p.Pro594Arg | 2 | No | |
p.Val611Met | 3 | No | |
p.Gly683Asp | 2 | No | |
TPR-like domain | p.Ala994Val | 2 | No |
p.Ala1007Thr | 2 | No | |
p.Arg1016Cys | 4 | No | |
p.His913Arg | 3 | No | |
p.Ser1000Pro | 4 | No | |
p.Asp1054_Ala1055 delins Glu | 2 | No | |
1 | Yes | ||
p.lle988Phe | 2 | No | |
2 | Yes | ||
p.Asp1019Glu | 3 | No | |
1 | Yes | ||
RBS domain | p.Tyr1282His | 1 | No |
1 | Yes | ||
p.Ser1311Leu fsX7 | 1 | No | |
1 | Yes | ||
p.His1364Pro | 2 | No | |
p.Leu1367Pro | 3 | No | |
3 | Yes |
Abbreviation: TPR, tetratricopeptide repeat.
DISCUSSIONBrain abnormalities are the most common clinical manifestation of GEMIN5-related neurodevelopmental disorders. Only one fifth of patients had seizures before 1 year old, mostly in the neonatal period (Francisco-Velilla et al., 2022; Ibrahim et al., 2023; Kour et al., 2021; Rajan et al., 2022; Saida et al., 2021). Seizures in the neonatal period are linked to genetic and structural congenital abnormalities, potentially worsening the condition (Zuberi et al., 2022). Most GEMIN5 gene mutation patients show cranial structural abnormalities, hinting at a link between seizures and disorder severity (Francisco-Velilla et al., 2022; Ibrahim et al., 2023; Kour et al., 2021; Rajan et al., 2022; Saida et al., 2021). In our study, we found that both cases had neonatal epilepsy onset, burst suppression on EEG, and multiple seizure forms.
This study describes two females with novel biallelic GEMIN5 variants inherited from asymptomatic parents who were predicted damaging or probably damaging using in silico tools. The two missense variants affect conserved residues observed in vertebrates. Patient symptoms overlap with reported GEMIN5 mutation cases, suggesting GEMIN5 variants as the cause (Ibrahim et al., 2023). Patients 1 and 2 share core GEMIN5 variant features like cerebellar hypoplasia and developmental delay. Additionally, both have EIDEE, corpus callosum dysgenesis, and drug-resistant epilepsy, new phenotypes. Patient 2 also has laryngeal chondrodysplasia, clubfoot, and hip dislocation. EIDEE prognosis varies, possibly evolving into different epilepsy syndromes (Guerrero Ruiz, 2022). Limited patient data hindered evolution summaries and prognostic comparisons, necessitating more GEMIN5-related cases and long-term follow-up for comprehensive evaluation.
We searched databases and found 5 articles on GEMIN5 variant patients, totaling 50 cases, with 47 showing cerebellar volume loss in MRI, a hallmark of NEDCAM syndrome (Francisco-Velilla et al., 2022; Ibrahim et al., 2023; Kour et al., 2021; Rajan et al., 2022; Saida et al., 2021) (Table S1). Eight had epilepsy, but it was not a focus previously. Five had seizures in the first year, and our two had neonatal seizures, suggesting a link between EIDEE and GEMIN5. Comparing our patients with literature cases, we found overlapping phenotypes from GEMIN5 mutations. Although the two missense variants were predicted to be damaging or probably damaging using in silico tools, we classified these variants as Variants of Unknown Significance because functional data are needed to conclude on their pathogenicity.
Variants p.Leu902Gln, p.Gln971Glu, p.Leu851fs30 in TPR-like domain, and p.Leu508 in WD40 repeat domain. EIDEE likely links to TPR-like variants, suggesting a genotype–phenotype correlation needing further study. Likely mechanism induced epilepsy may be that variants within TPR-like domain fail to associate with native ribosomes, hampering its involvement in translation control and establishing a functional difference with the wild-type protein (Francisco-Velilla et al., 2022). In addition, a study in drosophila speculated that the absence of any one member of the SMN–GEMIN complex is sufficient to arrest its function in a nucleocentric pathway, which is critical for motor function in vivo (Borg & Cauchi, 2013). This reinforces the crucial role of the GEMIN5 gene in the nervous system and the potential for its mutation to be a factor in the onset of neurological diseases. However, pathogenicity prediction via in silico tools needs confirmation through gene functional research.
Analysis of GEMIN5 variant patients shows TPR-like and RBS domain variants correlate with epilepsy (Table 3). A study showed that the variants in TPR-like domain disrupt protein dimerization, whereas the RBS1 variants confer protein instability. Besides, mutants in these two domains have defects in their interaction with protein networks involved in translation and RNA-driven pathways (Francisco-Velilla et al., 2022; Piñeiro et al., 2015). GEMIN5 expression differences may impact clinical phenotypes and severity (Saida et al., 2021). RNA-Seq analysis revealed that SMN1, GEMIN3, and GEMIN5 are linked to a common set of genetic pathways, including the tp53 and ErbB pathways. All three genes facilitate regeneration by inhibiting the ErbB pathway, thereby allowing cell proliferation in the injured neuromasts (Pei et al., 2020). However, factors affecting clinical heterogeneity in GEMIN5 patients need further study.
CONCLUSIONIn conclusion, we found novel biallelic variants of GEMIN5 in two individuals with EIDEE, dysgenesis of the corpus callosum and drug-resistant epilepsy, which expands the phenotypes and increases awareness of the association between GEMIN5 variants and epilepsy. The genotypes and variant locations help explain the phenotypic heterogeneity of patients with GEMIN5 variants.
AUTHOR CONTRIBUTIONSJing Zhang: Writing—original draft. Xinting Liu: Formal analysis. Gang Zhu: Writing—review and editing. Lin Wan: Conceptualization. Yan Liang: Methodology. Nannan Li: Investigation. Mingwei Huang: Validation. Guang Yang: Writing—review and editing; funding acquisition; project administration; resources; supervision; data curation; software; visualization.
ACKNOWLEDGMENTSThe authors are deeply grateful to the patients and clinicians who participated in this work.
CONFLICT OF INTEREST STATEMENTAll authors claim that there are no conflicts of interest.
FUNDING INFORMATIONGeneral Project of National Key Research and Development Program of China, Reference: 2023YFC2706405; Capital's Funds for Health Improvement and Research, Reference: 2024-2-5082; Beijing Natural Science Foundation, Reference: 7222187; Equipment Comprehensive Research Project of General Armament Department, Reference: 145BHQ090025000X; Key Project of Innovation Cultivation Fund of the Seventh Medical Center of Chinese PLA General Hospital, Reference: qzx-2023-1; Special Scientific Research Project of Military Family Planning, Reference: 22JSZ20.
DATA AVAILABILITY STATEMENTThe data that support the findings of this study are available in the Supporting Information section of this article or from the corresponding author upon reasonable request.
PEER REVIEWThe peer review history for this article is available at
The patients gave their informed consent for this report.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
© 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
Abstract
Background
Several biallelic truncating and missense variants of the gem nuclear organelle–associated protein 5 (GEMIN5) gene have been reported to cause neurodevelopmental disorders characterized by cerebellar atrophy, intellectual disability, and motor dysfunction. However, the association between biallelic GEMIN5 variants and early-infantile developmental and epileptic encephalopathies (EIDEEs) has not been reported.
Purpose
This study aimed to expand the phenotypic spectrum of GEMIN5 and explore the correlations between epilepsy and molecular sub-regional locations.
Methods
We performed whole-exome sequencing in two patients with EIDEE with unexplained etiologies. The damaging effects of variants were predicted using multiple in silico tools and modeling. All reported patients with GEMIN5 pathogenic variants and detailed neurological phenotypes were analyzed to evaluate the genotype–phenotype relationship.
Results
Novel biallelic GEMIN5 variants were identified in two unrelated female patients with EIDEE, including a frameshift variant (Hg19, chr5:154284147-154284148delCT: NM_015465: c.2551_c.2552delCT: p.(Leu851fs*30)), a nonsense mutation (Hg19, chr5:154299603-154299603delTinsAGA: NM_015465: c.1523delTinsAGA: p.(Leu508*)), and two missense variants (Hg19, chr5:154282663T > A: NM_015465: c.2705T > A: p.(Leu902Gln) and Hg19, chr5:154281002C > G: NM_015465: c.2911C > G: p.(Gln971Glu)), which were inherited from asymptomatic parents and predicted to be damaging or probably damaging using in silico tools. Except p.Leu508*, all these mutations are located in tetratricopeptide repeat (TPR) domain. Our two female patients presented with seizures less than 1 month after birth, followed by clusters of spasms. Brain magnetic resonance imaging suggests dysgenesis of the corpus callosum and cerebellar hypoplasia. Video electroencephalogram showed suppression-bursts. Through a literature review, we found 5 published papers reporting 48 patients with biallelic variants in GEMIN5. Eight of 48 patients have epilepsy, and 5 patients started before 1 year old, which reminds us of the relevance between GEMIN5 variants and EIDEE. Further analysis of the 49 GEMIN5 variants in those 50 patients demonstrated that variants in TPR-like domain or RBS domain were more likely to be associated with epilepsy.
Conclusions
We found novel biallelic variants of GEMIN5 in two individuals with EIDEE and expanded the clinical phenotypes of GEMIN5 variants. It is suggested that the GEMIN5 gene should be added to the EIDEE gene panel to aid in the clinical diagnosis of EIDEE and to help determine patient prognosis.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
Details




1 Senior Department of Pediatrics, The Seventh Medical Center of Chinese PLA General Hospital, Beijing, China; Department of Pediatrics, The First Medical Center of Chinese PLA General Hospital, Beijing, China; Medical School of Chinese People's Liberation Army, Beijing, China
2 Aegicare (Shenzhen) Technology Co., Ltd, Shenzhen, China
3 Senior Department of Pediatrics, The Seventh Medical Center of Chinese PLA General Hospital, Beijing, China; Department of Pediatrics, The First Medical Center of Chinese PLA General Hospital, Beijing, China; Medical School of Chinese People's Liberation Army, Beijing, China; The Second School of Clinical Medicine, Southern Medical University, Guangzhou, China