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    • Keywords


      temporal lobe epilepsy; betaine/GABA transporter-1; polymorphism; interaction; expression.

    • Abstract


      Temporal lobe epilepsy (TLE) is the most common epilepsy subtype with complex genetic structure. A recent study in four populations (Ireland, UK, Australia and Finland) reported an allelic association between betaine/GABA transporter-1 (𝐵𝐺𝑇-1 or 𝑆𝐿𝐶6𝐴12) and mesial temporal lobe epilepsy with hippocampal sclerosis. To demonstrate the association between 𝑆𝐿𝐶6𝐴12 gene polymorphisms and TLE, TaqMan method was used to genotype five single-nucleotide polymorphisms of 𝑆𝐿𝐶6𝐴12 gene in 358 TLE patients and 596 nonepileptic control subjects of Chinese Han origin. Real-time PCR was used to detect the effects of variations on gene expression associated with TLE. Though, the single-marker analysis did not demonstrate allelic association with TLE, rs542736–rs557881 interaction showed significant association. The 𝑆𝐿𝐶6𝐴12 expression levels in peripheral blood mononuclear cells were significantly higher in TLE patients than in control subjects and were correlated to rs542736 G–rs557881 A haplotypes. Our preliminary results suggested combined effect of two common polymorphisms on SLC6A12 gene may be associated with TLE, but the precise mechanism needs further investigation.

    • Author Affiliations


      Jingyun Li1 Hua Lin2 Fenghe Niu1 Xilin Zhu1 Ning Shen1 Xin Wang1 Liping Li2 Aihua Liu2 Xiaopan Wu1 Wei Sun2 Yuping Wang2 Ying Liu1

      1. National Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences, Chinese Academy of Medical Sciences; School of Basic Medicine, Peking Union Medical College, Beijing 100005, People’s Republic of China
      2. Department of Neurology, Xuanwu Hospital, Capital Medical University, Beijing 100053, People’s Republic of China
    • Dates

  • Journal of Genetics | News

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      Posted on July 25, 2019

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