Role of major and brain-specific Sgce isoforms in the pathogenesis of myoclonus-dystonia syndrome

NEUROBIOLOGY OF DISEASE

卷:98

Article

Xiao, Jianfeng¹  Vemula, Satya R.¹  Xue, Yi¹  Khan, Mohammad M.¹  Carlisle, Francesca A.²  Waite, Adrian J.²  Blake, Derek J.²  Dragatsis, Ioannis³  Zhao, Yu¹  LeDoux, Mark S.^1,4 

[1] Univ Tennessee, Hlth Sci Ctr, Dept Neurol, 847 Monroe Ave,Suite 226 Johnson Bldg, Memphis, TN 38163 USA

[2] Cardiff Univ, Sch Med, MRC Ctr Neuropsychiat Genet & Gen, Cardiff CF24 4HQ, S Glam, Wales

[3] Univ Tennessee, Hlth Sci Ctr, Dept Physiol, Memphis, TN 38163 USA

[4] Univ Tennessee, Hlth Sci Ctr, Dept Anat & Neurobiol, Memphis, TN 38163 USA

关键词: Sgce;    Dystonia;    Myoclonus;    Sarcoglycans;    Gene trap;   

DOI  :  10.1016/j.nbd.2016.11.003

来源: Elsevier

【 摘 要 】

Loss-of-function mutations in SGCE, which encodes epsilon-sarcoglycan (epsilon-SG), cause myoclonus-dystonia syndrome (OMIM159900, DYT11). A major epsilon-SG protein derived from CCDS5637.1 (NM_003919.2) and a brain-specific protein, that includes sequence derived from alternative exon 11b (CCDS47642.1, NM_001099400.1), are reportedly localized in post- and pre-synaptic membrane fractions, respectively. Moreover, deficiency of the brain-specific isoform and other isoforms derived from exon 11b may be central to the pathogenesis of DYT11. However, no animal model supports this hypothesis. Gene-trapped ES cells (CMHD-GT_148G1-3, intron 9 of NM_011360) were used to generate a novel Sgce mouse model (C57BL/6J background) with markedly reduced expression of isoforms derived from exons 3' to exon 9 of NM_011360. Among those brain regions analyzed in adult (2 month-old) wild-type (WT) mice, cerebellum showed the highest relative expression of isoforms incorporating exon 11b. Homozygotes (Sgce(Gt(148G1)Cmhd/Gt(148G1)Cmhd) or Sgce(Gt/Gt)) and paternal heterozygotes (Sgce(m+/pGt), m-maternal, p-paternal) showed 60 to 70% reductions in expression of total Sgce. Although expression of the major (NM_011360) and brain-specific (NM_001130189) isoforms was markedly reduced, expression of short isoforms was preserved and relatively small amounts of chimeric epsilon-SG/beta-galactosidase fusion protein was produced by the Sgce gene-trap locus. Immunoaffinity purification followed by mass spectrometry assessments of Sgce(m+/pGt) mouse brain using pan- or brain-specific epsilon-SG antibodies revealed significant reductions of epsilon-SG and other interacting sarcoglycans. Genome-wide gene-expression data using RNA derived from adult Sgce(m+/pGt) mouse cerebellum showed that the top up-regulated genes were involved in cell cycle, cellular development, cell death and survival, while the top down-regulated genes were associated with protein synthesis, cellular development, and cell death and survival. In comparison to WT littermates, Sgce(m+/pGt) mice exhibited tiptoe gait and stimulus-induced appendicular posturing between Postnatal Days 14 to 16. Abnormalities noted in older Sgce(m+/pGt) mice included reduced body weight, altered gait dynamics, and reduced open-field activity. Overt spontaneous or stimulus-sensitive myoclonus was not apparent on the C57BL/6J background or mixed C57BL/6J-BALB/c and C57BL/6J-129S2 backgrounds. Our data confirm that mouse Sgce is a maternally imprinted gene and suggests that short Sgce isoforms may compensate, in part, for deficiency of major and brain-specific Sgce isoforms. (C) 2016 Elsevier Inc. All rights reserved.

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