Pathogenetic Potential of the Mutations of SPTAN 1

Valentina Rapaccini1,2, Francesco Miconi3,4, Susanna Esposito5, Augusto Pasini1,2

1Child Neurology and Psychiatry Unit, Systems Medicine Department, University Hospital Tor Vergata, Viale Oxford 81, Rome, Italy

2Unità Sanitaria Locale (USL) Umbria 2, Viale VIII Marzo, Terni, Italy

3Paediatric Section, Università degli Studi di Perugia, Perugia, Italy

4Paediatric Clinic, Azienda Ospedaliera di Terni, Terni, Italy

5Department of Surgical and Biomedical Sciences, Paediatric Clinic, Università degli Studi di Perugia, Perugia, Italy

Recent evidence demonstrates that mutations in numerous genes such as SPTAN1 are responsible for early-onset epileptic encephalopathies, previously considered as cryptogenic1. SPTAN1, located on 9q34.11 chromosome, encodes a subtype of an α spectrin that is specifically expressed in nonerythrocytic cells. Spectrins are a large family of filamentous cytoskeletal proteins that contribute to stabilize the plasma membrane and organize intracellular organelles. They consist of α and β dimers that form tetramers linked in a head-to-head arrangement. The specific protein encoded by SPTAN1 in also implicated in other cellular functions including DNA repair and cell cycle regulation.

As mentioned above, mutations of SPTAN1 are considered responsible for early infantile epileptic encephalopathies and alternate splicing of this gene results in multiple transcript variants. In particular specific in-frame mutation of SPTAN1, altering the sensibility of voltage-gated sodium channels, can determine an elevated action potential threshold that is implicated in the generation of early epileptic events2. This effect is due to an abnormal aggregation of α-II mutant/β-II and α-II/β-III spectrin heterodimers. In fact, α-II spectrin consists of α and β subunits, is assembled in an antiparallel side by side manner into heterodimers that can form end-to-end tetramers integrating into the membrane cytoskeleton.

Recently in mouse models it has been shown that αII spectrin is ubiquitously expressed in rodent and human somatodendritic and axonal domains suggesting that αII spectrin is involved in critical aspects of nervous development and synaptogenesis and supporting a dominant-negative mechanism of SPTAN1 mutations in early infancy epileptic encephalopathy3.

Currently, genetic analysis demonstrated that mutations in the last two spectrin repeats, required for α/β spectrin heterodimer associations, can compromise heterodimer formation between the two spectrins. It has been demonstrated that only in-frame SPTAN1 mutations in the last two spectrin repeats in the C-terminal region can lead to dominant negative effects and severe specific phenotypes4.

SPTAN1 mutations are associated with various neurodevelopmental phenotypes, ranging from mild to severe and progressive. The typical clinical manifestations are often characterized by epileptic encephalopathy with seizures, hypsarrhythmia, poor visual attention, acquired microcephaly, spastic quadriplegia and severe intellectual disability, in addition to brainstem and cerebellar atrophy and cerebral hypomyelination, that can be evaluated by magnetic resonance imaging. The most severe mutations typically cause early onset epileptic encephalopathy characterized by infantile spasms or tonic seizures5.

Imaging studies suggested that the severity of neurological impairment and epileptic phenomena correlates with structural abnormalities and with both mutation type and location. Moreover, this clinical picture is often related to Early Onset West Syndrome, a common infantile epileptic syndrome that in some cases can be associated with SPTAN1 mutation6.

In particular, according to a recent study7, the vast majority of patients affected by SPTAN1 mutation exhibit epilepsy and in particular, in the subjects who suffered from an early infantile epileptic encephalopathy infantile, spasms were the most prominent seizure type represented. Infantile spasms manifested at a median age of 4 months (ranging from neonatal onset to 9 months) and occurred in the context of an infantile epileptic encephalopathy or as part of West syndrome accompanied by hypsarrhythmia on EEG. They generally persisted and also were highly refractory to treatment. Hypotonia were also present and could be considered an early sign of abnormal development. In general, most individuals with infantile epileptic encephalopathy exhibit profound developmental delay with quadriplegia and absent speech, often accompained by lack of visual contact and movement disorder, such as opisthotonic posturing or dyskinetic movements.

Therefore, as mentioned above, phenotypes associated with SPTAN1 mutations are various, ranging from mild to severe and progressive. In particular, spectrin aggregate formation in fibroblasts with mutations in the a/b heterodimerization domain seems to be associated with a severe neurodegenerative course and suggests that the amino acid stretch from Asp2303 to Met2309 in the a20 repeat is important for a/b spectrin heterodimer formation and/or aII spectrin function. Moreover, recently four different in-frame SPTAN1 mutations have been identified in association with different clinical features, from a milder variant characterized by generalized epilepsy with pontocerebellar atrophy to severe phenotypes, generally associated with in-frame SPTAN1 mutations in the last two spectrin repeats in the C-terminal region.

The functional impact of the identified variants can be predicted by two different methods: the Combined Annotation Dependent Depletion (CADD) and Rare exome variant ensemble learner (REVEL) scoring systems. CADD is a framework integrating multiple annotations into one metric by contrasting variants that survived natural selection with simulated mutations based upon all possible nucleotide variants. The higher the CADD score the more likely the variant has deleterious effects; the score obtained in SPTAN 1 mutations is in most cases highly predictive of pathogenicity8. REVEL is an ensemble method predicting the pathogenicity of missense variants with the possibility to distinguish pathogenic from rare neutral variants. The higher the score the more likely the variant is pathogenic9.

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  2. Saitsu H, Tohyama J, Kumada T, et al. Dominant-negative mutations in alpha-II spectrin cause West syndrome with severe cerebral hypomyelination, spastic quadriplegia, and developmental delay. Am J Hum Genet. 2010 Jun 11; 86(6): 881-91. doi: 10.1016/j.ajhg.2010.04.013. Epub 2010 May 20.
  3. Wang Y, Ji T, Nelson AD, et al. Critical roles of αII spectrin in brain development and epileptic encephalopathy. J Clin Invest. 2018 Feb 1; 128(2): 760-773. doi: 10.1172/JCI95743. Epub 2018 Jan 16.
  4. Hamdan FF, Saitsu H, Nishiyama K, et al. Identification of a novel in-frame de novo mutation in SPTAN1 in intellectual disability and pontocerebellar atrophy. Eur J Hum Genet. 2012 Jul; 20(7): 796-800. doi: 10.1038/ejhg.2011.271. Epub 2012 Jan 18.
  5. Ioannidis NM, Rothstein JH, Pejaver V, et al. REVEL: An Ensemble Method for Predicting the Pathogenicity of Rare Missense Variants. Am J Hum Genet. 2016 Oct 6; 99(4): 877-885. doi: 10.1016/j.ajhg.2016.08.016. Epub 2016 Sep 22.
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  7. Syrbe S, Harms FL, Parrini E, et al. Delineating SPTAN1 associated phenotypes: from isolated epilepsy to encephalopathy with progressive brain atrophy. Brain. 2017 Sep 1; 140(9): 2322-2336. doi: 10.1093/brain/awx195.
  8. Kircher M, Witten DM, Jain P, et al. A general framework for estimating the relative pathogenicity of human genetic variants. Nature Genetics. 2014; 46(3): 310.
  9. Writzl K, Primec ZR, Strazisar BG, et al. Early onset West syndrome with severe hypomyelination and coloboma-like optic discs in a girl with SPTAN1 mutation. Epilepsia. 2012 Jun; 53(6): e106-10. doi: 10.1111/j.1528-1167.2012.03437.x. Epub 2012 Mar 1.

Article Info

  • Journal of Human and Clinical Genetics
  • Article Type : Mini Review
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Article Notes

  • Published on: February 18, 2019


  • Pathogenetic

  • Nonerythrocytic cells


Dr. Valentina Rapaccini
Child Neurology and Psychiatry Unit, Systems Medicine Department, University Hospital Tor Vergata, Viale Oxford 81, Rome, Italy

©2019 Rapaccini V. This article is distributed under the terms of the Creative Commons Attribution 4.0 International License.