Homozygous frameshift BRAT1 mutations were found in patients with lethal neonatal rigidity and multifocal seizure syndrome (MIM# 614498). Here, we report on two siblings with compound heterozygous mutations in BRAT1. They had intractable seizures from neonatal period, dysmorphic features and hypertonia. Progressive microcephaly was also observed. Initial electroencephalogram showed a suppression-burst pattern, leading to a diagnosis of Ohtahara syndrome. They both died from pneumonia at 1 year and 3 months, respectively. Whole-exome sequencing of one patient revealed a compound heterozygous BRAT1 mutations (c.176T>C (p.Leu59Pro) and c.962_963del (p.Leu321Profs*81)). We are unable to obtain DNA from another patient. The p.Leu59Pro mutation occurred at an evolutionarily conserved amino acid in a CIDE-N (N-terminal of an cell death-inducing DFF45-like effector) domain, which has a regulatory role in the DNA fragmentation pathway of apoptosis. Our results further support that mutations of BRAT1 could lead to epileptic encephalopathy.
BRAT1 at 7p22.3 encodes BRCA1-associated ATM (ataxia telangiectasia mutated) activator 1, which binds to both the tumor suppressing BRCA1 protein and ATM protein, and has important roles in sensing of DNA damaged lesions.1,2 Recently, homozygous frameshift mutations in BRAT1 have been reported to cause lethal neonatal rigidity and multifocal seizure syndrome (MIM# 614498) in three patients from three separate Amish sibships and another from a consanguineous Mexican family.3,4 Here, we present Japanese siblings with compound heterozygous mutations in BRAT1.
She was born to non-consanguineous Japanese parents as a first child without asphyxia after a 40-weeks' pregnancy (Figure 1a). Birth weight was 2644 g (−1.15 standard deviation (s.d.)) and head circumference (HC) 32.7 cm (−0.55 s.d.). Muscle hypertonia, micrognathia, short and webbed neck and dysmorphic face were observed at birth. Laboratory examination did not reveal any abnormalities. Serial seizures of her arms and legs twitching started at age 7 days, followed by generalized tonic clonic convulsions. Electroencephalography showed suppression-burst pattern, leading to diagnosis of Ohtahara syndrome or early myoclonic encephalopathy. Phenobarbital and clonazepam were not effective. Apnea attacks appeared at the age of 2 months. Zonisamide controlled her apnea attacks and general tonic convulsion at 8 months, but myoclonic seizures of the limbs and face were persistent. Her HC at 10 months is 43.0 cm (−2.3 s.d.). Serial brain magnetic resonance imaging revealed progressive cerebral and cerebellar atrophy (Figures 1b, c, e and f), and funduscopic examination revealed optic atrophy. She showed hypertonia, hyperreflexia and foot clonus, but no developmental milestones. She died of pneumonia at the age of 1 year and 9 months.
She was born after 39 weeks’ gestation without asphyxia as a younger sister to case II-1. Her birth weight was 2540 g (−1.40 s.d.), height 45.5 cm (−1.84 s.d.) and HC 32 cm (−0.93 s.d.). Muscle hypertonia, generalized myoclonic seizures and partial clonic convulsions, poor voluntary movements, and dysmorphic features including bilateral talipes equinovarus, a round face, a thin lip and large ears were observed soon after birth. Exaggerated deep-tendon reflexes and Babinski reflex were also observed. Irritabilities and myoclonus of the limbs were readily induced by stimulation. Chromosomal analysis and laboratory examination showed no abnormalities.
In her clinical course, her various convulsions consisted of myoclonic, clonic and tonic seizures, which were worsen by phenytoin. Apnea attacks increased at day 53, which were relieved by zonisamide. Brain magnetic resonance imaging at 3 months showed mild cerebral and cerebellar atrophy, and delayed myelination of the cerebral white matter (Figures 1d and g). Initial electroencephalography at second day of birth showed suppression-burst pattern (Figure 1h). Optic atrophy was detected by funduscopy. She obtained no developmental milestones even without swallowing her own saliva, thereafter died of pneumonia at the age of 3 months. The weight and the HC were 4884 g (−1.6 s.d.) and 35 cm (−3.8 s.d.), respectively. An autopsy was performed.
Neuropathological findings of case II-2
The brain weight was 321 g, much smaller than that of age-matched control brain (718 g). The cerebellum was proportionately small. No cortical dysgenesis was seen, but cortical neurons were moderately depleted. Remaining neurons showed no substance accumulation inside (Figures 1i and j). The entire white matter of the cerebrum showed moderate gliosis and no myelination in the frontal lobe (Figure 1k). The moderate Purkinje cells depletion and some dendritic expansions were observed in the cortical layer of the cerebellum. The neurons of the dentate nucleus were also depleted. No calcification was found in the caudate and globus pallidus but tiny microglial nodule in the thalamus. No specific neuronal loss was observed in hippocampal area. Neuronal cells of the brain stem, including pontine nuclei and olivary nuclei, were preserved relatively. Myelination of brain stem and spinal cord was developed well.
Results and Discussion
Genomic DNA of liver tissues of case II-2 was captured using the SureSelect Human All Exon v5 Kit (Agilent Technologies, Santa Clara, CA, USA), and sequenced with on HiSeq2000 (Illumina, San Diego, CA, USA) with 101 bp paired-end reads. Exome data processing was performed as previously described.5 Coverage data and variant filtering are shown in Supplementary Table S1. Among 19 genes possessing two heterozygous variants (possible compound heterozygous mutations) or a homozygous mutation based on the autosomal recessive model, we found two mutations in BRAT1. Compound heterozygosity of the two mutations was confirmed by Sanger sequencing: c.176T>C (p.Leu59Pro) and c.962_963del (p.Leu321Profs*81) were transmitted from her father and mother, respectively. These two mutations were not found in the ESP6500 exomes or among our 575 in-house control exomes. The p.Leu59Pro mutation was predicted as damaging by sorting intolerant from tolerant (SIFT), PolyPhen2 and MutationTaster (Supplementary Table S2). All experimental protocols used were approved by the Institutional Review Board of Yokohama City University School of Medicine.
BRAT1, also donated as BAAT1, is identified as a binding protein with BRCA1 and ATM. The role of BRAT1 is under investigation, but is considered to have roles in sensing of DNA damaged lesions and apoptosis.1,2 To date, two homozygous frameshift mutations (c.638dupA and c.453_454insATCTTCTC) have been reported in a total of four families in which three Amish families were likely to be related (Figure 2).3,4 The affected individuals including our cases commonly showed hypertonia, intractable seizures, microcephaly and early lethality. Although we are unable to check the BRAT1 mutations in case II-1 as biological samples were unavailable, these striking similarities of clinical features suggest that she also had two BRAT1 mutations, which are highly likely to be pathogenic. It is interesting to note that the p.Leu59Pro mutation occurred in an evolutionarily conserved (chemically similar) amino acid within N-terminal of an cell death-inducing DFF45-like effector (CIDE-N) domain (Figure 2). Indeed, the CIDE-N domain is known to have a regulatory role in the DNA fragmentation pathway of apoptosis.6 Considering the fact that progressive atrophy and neuronal cell loss were observed in cerebrum and cerebellum, aberration of apoptosis may be one of pathologies caused by BRAT1 mutations.
In conclusion, we describe two Japanese girls with Ohtahara syndrome, possessing compound heterozygous BRAT1 mutations. Our report suggests that regulation of apoptosis by BRAT1 may be important for normal brain development.
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We would like to thank the patient and her family for their participation in this study. We thank Nobuko Watanabe for her technical assistance. This study was supported by: the Japanese Ministry of Health, Labour, and Welfare; the Japan Society for the Promotion of Science (a Grant-in-Aid for Scientific Research (B) (25293085, 25293235), a Grant-in-Aid for challenging Exploratory Research (26670505); a Grant-in-Aid for Scientific Research (A) (13313587)); the Takeda Science Foundation; the fund for Creation of Innovation Centers for Advanced Interdisciplinary Research Areas Program in the Project for Developing Innovation Systems; the Strategic Research Program for Brain Sciences (11105137); and a Grant-in-Aid for Scientific Research on Innovative Areas (Transcription Cycle) from the Japanese Ministry of Education, Culture, Sports, Science, and Technology (12024421).
The authors declare no conflict of interest.
Supplementary Information accompanies the paper on Journal of Human Genetics website
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Saitsu, H., Yamashita, S., Tanaka, Y. et al. Compound heterozygous BRAT1 mutations cause familial Ohtahara syndrome with hypertonia and microcephaly. J Hum Genet 59, 687–690 (2014). https://doi.org/10.1038/jhg.2014.91
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