A novel de novo truncating TRIM8 variant associated with childhood-onset focal segmental glomerulosclerosis without epileptic encephalopathy: a case report
BMC Nephrology volume 22, Article number: 417 (2021)
Heterozygous truncating variants in the Tripartite motif containing 8 (TRIM8) gene have been reported to cause epileptic encephalopathy, both with and without proteinuria. A recent study showed a lack of TRIM8 protein expression, with suppressor of cytokine signaling 1 (SOCS1) overexpression, in podocytes and tubules from a patient with a TRIM8 variant, who presented with epileptic encephalopathy and focal segmental glomerulosclerosis (FSGS). To date, no patients with TRIM8 variants who presented with nephrotic syndrome but without neurological manifestations have been described.
An 8-year-old girl presented with nephrotic syndrome, without epilepsy or developmental delay. Her kidney biopsy specimens showed FSGS and cystic dilatations of the distal tubules. Whole-exome sequencing identified a novel de novo heterozygous variant in the C-terminal encoding portion of TRIM8 (c.1461C > A), resulting in a premature stop codon (p.Tyr487*). Reverse transcription-polymerase chain reaction using peripheral blood mononuclear cells identified the mRNA sequence of the mutant allele, which confirmed an escape from nonsense-mediated mRNA decay. Immunofluorescence studies showed a lack of TRIM8 expression in glomerular and tubular cells and cystic dilatation of distal tubules. Immunohistochemical studies showed overexpression of SOCS1 in glomerular and tubular cells.
We reported a patient with FSGS, associated with a de novo heterozygous TRIM8 variant, without any neurological manifestations. Our results expanded the clinical phenotypic spectrum of TRIM8 variants.
Sakai et al. described a 10-year-old boy with epileptic encephalopathy, severe developmental delay, and a de novo variant the tripartite motif containing 8 (TRIM8) gene . Assoum et al. described five additional individuals of childhood-onset epileptic encephalopathy associated with heterozygous de novo variants in the C-terminus-encoding portion of TRIM8, including three individuals who presented with proteinuria . Recently, Warren et al. reported an individual with epileptic encephalopathy and nephrotic syndrome with a TRIM8 variant, and his kidney specimen showed FSGS . They also performed immunohistochemical (IHC) staining, using an anti-TRIM8 antibody, and demonstrated a lack of TRIM8 protein expression, with suppressor of cytokine signaling 1 (SOCS1) overexpression, which is regulated by TRIM8, in the podocytes and tubules . In addition, McClatchey et al. presented an individual with FSGS which required renal replacement therapies, but only mild neurodevelopmental problems .
Here, we report a patient with a novel, de novo, heterozygous nonsense variant in the last exon of TRIM8, who presented with nephrotic range proteinuria and progressed to end-stage renal disease (ESRD) but did not present with any neurological manifestations. A kidney biopsy showed FSGS and cystic dilatations of the tubules. To evaluate pathogenicity of the patient’s nonsense TRIM8 variant and characterize the pathological changes in glomerular and tubulointerstitial lesions, we performed mRNA analysis in mononuclear cells and immunofluorescence studies on kidney specimens from the present patient and control samples. In addition, the loci of TRIM8 nonsense variants and clinical manifestations in previously reported individuals and the present patient were reviewed.
A girl presented with asymptomatic proteinuria, which was revealed by a urinary screening test performed in Japan when she was 3 years old. She had no family history of renal or neurological disorders. The urine protein to creatinine ratio (UPCR) was 1.0–1.5 g/gCr (reference range < 0.2 g/gCr) at that time. Ultrasonography revealed normal echogenicity in both kidneys. She developed nephrotic syndrome, without systemic edema, at the age of 8 years. Polyuria and polydipsia with a urine output of 3L in a day were also documented. UPCR was 11.5 g/gCr, and the serum albumin level was 2.1 g/dL (reference range 3.7–5.5 g/dL). The serum creatinine level was 0.97 mg/dL (eGFR was 46.8 mL/min/1.73m2). The urine specific gravity was 1.008, and urinary beta 2-microglobulin increased to 9,269 µg/L (reference range ≤ 150 μg/L). A kidney biopsy revealed that 13 (52%) of 25 glomeruli showed segmental or global sclerosis. Furthermore, two glomeruli showed cellular lesions, which were characterized by swollen, vacuolated, and proliferative glomerular epithelial cells, throughout Bowman’s space. The underlying glomerular capillaries were partially collapsed and occluded by swollen endothelial cells and karyorrhexis, which was consistent with a pathological diagnosis of FSGS (Fig. 1A) . No glomeruli with collapse and overlying podocyte hypertrophy and hyperplasia were not observed. Cystic dilatations of the tubules and interstitial fibrosis were also observed (Fig. 1B). The patient presented with no neurological manifestations, such as seizures or developmental delays. Brain magnetic resonance imaging (MRI) and electroencephalogram detected no abnormalities. She could hold her head up at 4 months old, sit at 8 months old, pull up to stand at 9 moths and speak single words at 1 year and 6 months old. She did not need special support to attend school. Her renal function continued to deteriorate, and she eventually developed ESRD, despite the administration of angiotensin receptor blockers. At 9 years of age, pre-emptive kidney transplantation was performed, with a kidney donated by her mother. No recurrence of proteinuria has been observed for 1 year and 9 months after transplantation.
We performed whole-exome analysis using a previously described method , focusing on variants in the genes that are currently known to cause FSGS or nephronophthisis (Tables S1 and S2), and identified a de novo novel heterozygous C to A transition (c.1461C > A) in the last exon of TRIM8, resulting in a premature stop codon (p.Tyr487*). The alternative and reference allele counts were 68 (46%) and 80 (54%), respectively. Sanger sequencing showed that the individual had the variant but that her parents did not. This variant was absent in population databases including the Exome Aggregation Consortium database (ExAC, http://exac.broadinstitute.org/), Genome Aggregation Database (gnomAD, http://gnomad.broadinstitute.org), 1000 Genomes (1000G, http://asia.ensembl.org/Homo_sapiens/Info/Index), ESP6500 (http://evs.gs.washington.edu/EVS/). No additional pathogenic variants in the genes that are currently known to cause FSGS or nephronophthisis were identified (Tables S1 and S2). This variant was classified as pathogenic (PVS1, PM1, PM2, PM6, and PP4) based on the criteria developed by the American College of Medical Genetics and Genomics .
The sequence analysis of mRNA was performed as previouly reported methods . RNA was extracted from peripheral blood mononuclear cells with the RNeasy Mini Kit (QIAGEN), according to the manufacturer’s instructions. The RNA was treated with DNase (QIAGEN) to avoid genomic DNA contamination, and 200 ng of total RNA was reverse transcribed, using the SuperScript VILO cDNA Synthesis Kit (Thermo Fisher Scientific) for the mRNA analysis. The following primers were used to amplify and sequence exon 6 of TRIM8 from cDNA: 5’-GAGTGTCCCCCTGTACCCTT -3’ (forward) and 5’-CTACAGGGTGTATGGGCAGC-3’ (reverse). Polymerase chain reaction experiments were performed, using Invitrogen Platinum II Taq Hot-Start DNA Polymerase (Thermo Fisher Scientific) and T100TM Thermal Cycler (Bio-Rad Laboratories) identifing mRNA sequences transcribed from the TRIM8 mutant allele (Fig. 2), which confirmed the escape from nonsense-mediated mRNA decay (NMD) .
Immunohistochemical analysis were performed using the formalin-fixed paraffin-embedded kidney biopsy specimens obtained from the present patient and nine control individuals consisting of three living kidney transplantation donors who served as normal controls, five patients with primary FSGS and one patient with nephronophthisis who served as disease controls. We performed autoclave-based antigen retrieval, for 15 min at 105 °C, in Bond Epitope Retrieval Solution 2 (Leica Biosystems Newcastle, Ltd., Newcastle Upon Tyne, UK). Specimens were incubated with goat polyclonal antibody against an epitope corresponding to amino acids 540–551, at the C-terminus of human TRIM8 (Abcam, Cambridge, MA, USA; catalog no. ab4302), overnight, at a dilution of 1:500 . Immunofluorescence staining, using the anti-TRIM8 antibody in normal control specimens, is shown in Fig. 3 (Fig. 3A–E). TRIM8 expression was observed in the nuclei of all glomerular cells (Fig. 3A–C). Double immunostaining with mouse anti-human podocalyxin monoclonal antibody (PHM5, Merck Millipore, Darmstadt, Germany), at a dilution of 1:100 which was used as a podocyte marker (Fig. 3B)  and mouse anti-human cluster of differentiation 34 (CD34) monoclonal antibody (QBEND/10, Leica Microsystems, Wetzlar, Germany), at a dilution of 1:40 which was used as an endothelial cell marker (Fig. 3C)  showed that TRIM8 was expressed in the nuclei of podocytes and endothelial cells, respectively. Proximal tubular cells that were identified by mouse anti-human cluster of differentiation 10 (CD10) monoclonal antibody (56C6, Leica Microsystems, Wetzlar, Germany) without dilution  and distal tubular cells that were identified by mouse anti-human epithelial membrane antigen (EMA) monoclonal antibody (Clone E29, Dako, Santa Clara, California, USA) without dilution  also showed the nuclear expression of TRIM8 protein (Fig. 3D and E). Similar findings were observed in specimens from disease controls (Fig. S1). In contrast, the present patient showed a lack of TRIM8 protein expression in any cells in the glomeruli and tubules (Fig. 3F–J). The tubules showing cystic dilatation were positive for EMA, but negative for CD10, indicating that cystic dilatation was evident in the distal tubules (Fig. 3I and J). IHC staining, using anti-SOCS1 goat polyclonal antibody (Abcam, catalog no. ab9870), at a dilution of 1:500  of the kidney biopsy specimens derived from the present patient showed stronger cytoplasmic SOCS1 expression in glomerular and tubular cells than observed in control samples (Fig. S2).
Discussion and conclusions
We reported the first patient with a de novo variant in TRIM8 who developed nephrotic syndrome and ESRD without any neurological manifestations. Immunofluorescence examination indicated that the variant identified in the present case (p.Tyr487*) is pathogenic because TRIM8 expression was decreased in all kidney cells, consistent with a previous report . Additionally, sequence analysis of mRNA of samples from the present patient confirmed the escape of the mutant allele from NMD. These findings suggested a dominant-negative effect for the heterozygous nonsense variant, which could affect the E3 ubiquitin ligase activity of TRIM8 in the kidney [5, 16].
To date, at least eight reported individuals have been associated with heterozygous truncating variants in TRIM8, all of whom developed epilepsy or epileptic encephalopathy, including five individuals with proteinuria (Table 1 and Fig. 4) [3,4,5,6]. The present patient did not present with any neurological manifestations such as developmental delay and epilepsy. Brain MRI showed no abnormalities in the present patient, while cortical and subcortical atrophy and cysts in white matter on MRI have been described in the literature . Because whole-exome sequencing showed that alternative allele counts were approximately half of the total reads, it is unlikely that the individual was a mosaic. The locus of the truncating variant in the present patient (p.Tyr487*) was closest to the C-terminal end than variants in other reported individuals (Table 1 and Fig. 4, patient IX). Nevertheless, the variant of patient III, who had mild developmental delay and well-controlled epilepsy , was located more 5’ in the last exon than 5 patients with epileptic encephalopathy reported by Assoum et al. and Warren et al. [4, 5]. Therefore, a difference in the size of the truncated protein may not explain the difference in the severity of the neurological phenotype . However, proteinuria tended to be documented in those individuals featuring TRIM8 variants that affected regions closer to the C-terminal end of the TRIM8 protein (Table 1 and Fig. 4, patient III, V-IX). Three of five individuals with proteinuria developed ESRD during childhood [5, 6]. Very recently, Weng et al. reported 12 individuals with TRIM8 variants clustering within the last exon between residues 390 and 487 of the 551 amino acid protein. All of them presented with nephrotic syndrome and neurologic disease, ten of whom showed FSGS on kidney biopsies . ESRD occurred in 10 individuals at the age of 1 to 19 . One of them, who had the same heterozygous variant as our patient (p.Tyr487*), presented with childhood-onset FSGS and neurological manifestations such as mild developmental delay, Tourette’s syndrome-like symptoms, and autism spectrum . Collectively, these findings expanded the clinical phenotypic spectrum of TRIM8 variants.
Renal pathological assessment of the present patient showed FSGS (Fig. 1A) and cystic dilatation of the distal tubules (Fig. 1B, 3I and J), which may be associated with other manifestations observed in our patient, such as polyuria and hyposthenuria. Although no tubulointerstitial changes were described in the individual reported by Warren et al. , a lack of TRIM8 expression in the tubular cells was noticed in the report by Warren et al.  To examine the possible superimposition of nephronophthisis, we performed genetic testing and examined 83 nephronophthisis causative genes (Table S2). However, no pathogenic variants in the genes currently known to cause nephronophthisis were identified in the present patient. Further studies remain necessary to characterize tubulointerstitial changes in patients with TRIM8 variants.
The mechanism underlying proteinuria and the cystic dilatation of tubules observed in our patient remains largely unknown. In this study, TRIM8 expression was observed in the nuclei of podocytes and tubular cells of control specimens. TRIM8 has been shown to enhance the translocation of signal transducer and activator of transcription 3 (STAT3) into the nucleus, and TRIM8 modulates STAT3 transcriptional potential in the nucleus . Our study showed increased SOCS1 protein expression levels in kidney specimens from our patient, which was consistent with the report by Warren et al. Strong SOCS1 expression can inhibit cytokine signaling by binding to downstream signaling molecules such as Janus tyrosine kinases (JAK) , and inhibition of JAK/STAT3 activity attenuates the progression of glomerular and tubulointerstitial injury . However, the associations between the TRIM8, SOCS1 protein expression, and renal manifestations remain unknown. It has been also described that TRIM8 induces p53-dependent cell cycle arrest . Podocytes are terminally differentiated cells and have a limited capacity to divide. Wang et al. reported that the cellular lesion of FSGS is characterized by podocyte proliferation superimposed on sclerotic or collapsed glomerular tufts . Therefore, TRIM8 dysfunction in podocytes may be associated with aberrant regulation of cell cycle, which may lead to the progression of FSGS. Cell cycle dysregulation has been also demonstrated in renal tubular epithelial cells in autosomal dominant polycystic kidney disease (ADPKD) . Knockdown of Pkd1, a responsible gene for ADPKD, has been shown to reduce the amount of p53 and lower the fraction of cells in G1/S, suggesting that unchecked cell cycle progression is involved in the pathogenesis of tubular cyst growth . Collectively, aberrant regulation of cell cycle induced by TRIM8 abnormalities may cause FSGS and the cystic dilatation of renal tubules.
In conclusion, we reported a patient with FSGS who had a de novo heterozygous TRIM8 variant without any neurological manifestations. Our results expanded the clinical phenotypic spectrum of TRIM8 variants CD10, cluster of differentiation 10; CD34, cluster of differentiation 10; EMA, epithelial membrane antigen; ESRD, end-stage renal disease; JAK, Janus tyrosine kinases; NMD, nonsense-mediated mRNA decay; SOCS1, Suppressor of cytokine signaling 1; STAT3, signal transducer and activator of transcription 3; TRIM8, tripartite motif containing 8; UPCR, urine protein to creatinine ratio.
Availability of data and materials
The datasets are not publicly available but are available from the first author on reasonable request.
Cluster of differentiation 10
Cluster of differentiation 10
Epithelial membrane antigen
End-stage renal disease
Janus tyrosine kinases
Nonsense-mediated mRNA decay
Suppressor of cytokine signaling 1
Signal transducer and activator of transcription 3
Tripartite motif containing 8
Urine protein to creatinine ratio
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We express our thanks to Professor Toshiyuki Yamamoto, at the Institute of Medical Genetics, Tokyo Women’s Medical University for helpful discussions. This work was supported by Medical Research Institute (MRI), Tokyo Women’s Medical University. We thank Lisa Giles, PhD, from Edanz Group (https://en-author-services.edanzgroup.com/) for editing a draft of this manuscript.
This work was supported by MEXT/JSPS KAKENHI [Grant numbers JP18K07857 to M.H. and JP18K07830 to K.M.] from the Ministry of Education, Culture, Sports, Science and Technology of Japan. The funding body played no role in the design of the study, collection, analysis, and interpretation of the data, or in writing the manuscript.JP18K07857,JP18K07830
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The study was approved by the Institutional Review Board at Tokyo Women’s Medical University (approval number 376). The guardians of the patient provided written informed consent.
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Immunofluorescence staining of the disease controls. Immunofluorescence staining, using an anti-TRIM8 antibody (red) and 4′,6-diamidino-2-phenylindole (DAPI) (blue), in kidney specimens from a case with primary FSGS (a–d), and a case with nephronophthisis (e–h). TRIM8 protein was expressed in the nuclei of glomerular cells and tubular epithelial cells. (Original magnification, ×400. Scale bar = 50 µm). Figure S2. Immunohistochemical staining of SOCS1. Immunohistochemical staining, using an anti-SOCS1 antibody, in the present case and a normal control case. The present case showed stronger SOCS1 protein expression in the cytoplasm of glomerular and tubular epithelial cells (A) than the control case (B). (Original magnification, ×200. Scale bar = 50 µm). SOCS1, Suppressor of cytokine signaling 1. Table S1. The list of 65 genes which represent monogenic causes of human focal segmental glomerulosclerosis and/or steroid-resistant nephrotic syndrome. Table S2. The list of 83 genes which represent monogenic causes of human nephronophthisis
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Shirai, Y., Miura, K., Kaneko, N. et al. A novel de novo truncating TRIM8 variant associated with childhood-onset focal segmental glomerulosclerosis without epileptic encephalopathy: a case report. BMC Nephrol 22, 417 (2021). https://doi.org/10.1186/s12882-021-02626-1
- Focal segmental glomerulosclerosis
- Nonsense-mediated mRNA decay
- Suppressor of cytokine signaling 1
- Tripartite motif containing 8
- Case report