Epilepsy, behavioral abnormalities, and physiological comorbidities in syntaxin-binding protein 1 (STXBP1) mutant zebrafish

Brian P. Grone, Maria Marchese, Kyla R. Hamling, Maneesh G. Kumar, Christopher S. Krasniak, Federico Sicca, Filippo M. Santorelli, Manisha Patel, Scott C. Baraban

Research output: Contribution to journalArticle

31 Citations (Scopus)

Abstract

Mutations in the synaptic machinery gene syntaxin-binding protein 1, STXBP1 (also known as MUNC18-1), are linked to childhood epilepsies and other neurodevelopmental disorders. Zebrafish STXBP1 homologs (stxbp1a and stxbp1b) have highly conserved sequence and are prominently expressed in the larval zebrafish brain. To understand the functions of stxbp1a and stxbp1b, we generated loss-of-function mutations using CRISPR/Cas9 gene editing and studied brain electrical activity, behavior, development, heart physiology, metabolism, and survival in larval zebrafish. Homozygous stxbp1a mutants exhibited a profound lack of movement, low electrical brain activity, low heart rate, decreased glucose and mitochondrial metabolism, and early fatality compared to controls. On the other hand, homozygous stxbp1b mutants had spontaneous electrographic seizures, and reduced locomotor activity response to a movement-inducing "dark-flash" visual stimulus, despite showing normal metabolism, heart rate, survival, and baseline locomotor activity. Our findings in these newly generated mutant lines of zebrafish suggest that zebrafish recapitulate clinical phenotypes associated with human syntaxin-binding protein 1 mutations.

Original languageEnglish
Article numbere0151148
JournalPLoS One
Volume11
Issue number3
DOIs
Publication statusPublished - Mar 1 2016

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Qa-SNARE Proteins
epilepsy
Zebrafish
Danio rerio
Metabolism
Comorbidity
binding proteins
Epilepsy
Brain
Carrier Proteins
mutants
Locomotion
Clustered Regularly Interspaced Short Palindromic Repeats
Genes
Syntaxin 1
Mutation
Zebrafish Proteins
brain
Heart Rate
Physiology

ASJC Scopus subject areas

  • Agricultural and Biological Sciences(all)
  • Biochemistry, Genetics and Molecular Biology(all)
  • Medicine(all)

Cite this

Grone, B. P., Marchese, M., Hamling, K. R., Kumar, M. G., Krasniak, C. S., Sicca, F., ... Baraban, S. C. (2016). Epilepsy, behavioral abnormalities, and physiological comorbidities in syntaxin-binding protein 1 (STXBP1) mutant zebrafish. PLoS One, 11(3), [e0151148]. https://doi.org/10.1371/journal.pone.0151148

Epilepsy, behavioral abnormalities, and physiological comorbidities in syntaxin-binding protein 1 (STXBP1) mutant zebrafish. / Grone, Brian P.; Marchese, Maria; Hamling, Kyla R.; Kumar, Maneesh G.; Krasniak, Christopher S.; Sicca, Federico; Santorelli, Filippo M.; Patel, Manisha; Baraban, Scott C.

In: PLoS One, Vol. 11, No. 3, e0151148, 01.03.2016.

Research output: Contribution to journalArticle

Grone, BP, Marchese, M, Hamling, KR, Kumar, MG, Krasniak, CS, Sicca, F, Santorelli, FM, Patel, M & Baraban, SC 2016, 'Epilepsy, behavioral abnormalities, and physiological comorbidities in syntaxin-binding protein 1 (STXBP1) mutant zebrafish', PLoS One, vol. 11, no. 3, e0151148. https://doi.org/10.1371/journal.pone.0151148
Grone, Brian P. ; Marchese, Maria ; Hamling, Kyla R. ; Kumar, Maneesh G. ; Krasniak, Christopher S. ; Sicca, Federico ; Santorelli, Filippo M. ; Patel, Manisha ; Baraban, Scott C. / Epilepsy, behavioral abnormalities, and physiological comorbidities in syntaxin-binding protein 1 (STXBP1) mutant zebrafish. In: PLoS One. 2016 ; Vol. 11, No. 3.
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