2. Academic Validation
  3. Biochemical characterization of two novel mutations in the human high-affinity choline transporter 1 identified in a patient with congenital myasthenic syndrome

Biochemical characterization of two novel mutations in the human high-affinity choline transporter 1 identified in a patient with congenital myasthenic syndrome

  • Hum Mol Genet. 2023 Jan 5;ddac309. doi: 10.1093/hmg/ddac309.
Midhat Rizvi 1 2,  Tina K Truong 3,  Janet Zhou 2 4,  Manav Batta 1 2,  Ellen S Moran 5,  John Pappas 6,  Mary Lynn Chu 7,  Oana Caluseriu 8 9,  Gilad D Evrony 3 10,  Elaine M Leslie 1 2 4,  Emmanuelle Cordat 1 2
Affiliations

Affiliations

  • 1 Department of Physiology, University of Alberta, Edmonton, Alberta, Canada.
  • 2 Membrane Protein Disease Research Group, University of Alberta, Edmonton, Alberta, Canada.
  • 3 Center for Human Genetics and Genomics, New York University Grossman School of Medicine, New York, USA.
  • 4 Department of Laboratory Medicine and Pathology, University of Alberta, Edmonton, Alberta, Canada.
  • 5 Clinical Genetics, New York University Langone Orthopedic Hospital, New York, USA.
  • 6 Division of Clinical Genetics, Department of Pediatrics, New York University Grossman School of Medicine, New York, USA.
  • 7 Department of Neurology, New York University School of Medicine, New York, USA.
  • 8 Department of Medical Genetics, University of Alberta, Edmonton, Alberta, Canada.
  • 9 Department of Pediatrics, University of Alberta, Edmonton, Alberta, Canada.
  • 10 Department of Pediatrics, Department of Neuroscience and Physiology, New York University Grossman School of Medicine, New York, USA.
PMID: 36611016 DOI: 10.1093/hmg/ddac309
Abstract

Congenital myasthenic syndrome (CMS) is a heterogeneous condition associated with 34 different genes, including SLC5A7, which encodes the high affinity choline transporter 1 (CHT1). CHT1 is expressed in presynaptic neurons of the neuromuscular junction where it uses the inward sodium gradient to re-uptake choline. Bi-allelic CHT1 mutations often lead to neonatal lethality, and less commonly to non-lethal motor weakness and developmental delays. Here, we report detailed biochemical characterization of two novel mutations in CHT1, p.I294T and p.D349N, that we identified in an 11 year-old patient with a history of neonatal respiratory distress, and subsequent hypotonia and global developmental delay. Heterologous expression of each CHT1 mutant in human embryonic kidney cells showed two different mechanisms of reduced protein function. The p.I294T CHT1 mutant transporter function was detectable, but its abundance and half-life were significantly reduced. In contrast, the p.D349N CHT1 mutant was abundantly expressed at the cell membrane, but transporter function was absent. The residual function of the p.I294T CHT1 mutant may explain the non-lethal form of CMS in this patient, and the divergent mechanisms of reduced CHT1 function that we identified may guide future functional studies of the CHT1 myasthenic syndrome. Based on these in vitro studies that provided a diagnosis, treatment with cholinesterase inhibitor together with physical and occupational therapy significantly improved the patient's strength and quality of life.

Figures
Products
嗨！很高兴为您提供帮助！

尊敬的 MCE 客户您好，
请您选择所在区域，我们将转接对应客服为您服务！

热门区域

A

B

C

F

G

H

J

L

N

Q

S

T

X

Y

Z

热 A B C F G H J L N Q S T X Y Z