Functional analysis of SERCA1b, a highly expressed SERCA1 variant in myotonic dystrophy type 1 muscle

BIOCHIMICA ET BIOPHYSICA ACTA-MOLECULAR BASIS OF DISEASE

卷:1852

Article

Zhao, Yimeng¹  Ogawa, Haruo²  Yonekura, Shin-Ichiro²  Mitsuhashi, Hiroaki¹  Mitsuhashi, Satomi³  Nishino, Ichizo³  Toyoshima, Chikashi²  Ishiura, Shoichi¹ 

[1] Univ Tokyo, Grad Sch Arts & Sci, Dept Life Sci, Meguro Ku, Tokyo 1538902, Japan

[2] Univ Tokyo, Inst Mol & Cellular Biosci, Bunkyo Ku, Tokyo 1130032, Japan

[3] Natl Ctr Neurol & Psychiat, Natl Inst Neurosci, Dept Neuromuscular Res, Kodaira, Tokyo 1878551, Japan

关键词: SERCA1a;    SERCA1b;    Myotonic dystrophy;    P-type ATPase;    Alternative splicing;   

DOI  :  10.1016/j.bbadis.2015.07.006

来源: Elsevier

【 摘 要 】

Myotonic dystrophy type 1 (DM1) is a genetic disorder in which multiple genes are aberrantly spliced. Sarco/endoplasmic reticulum Ca2+-ATPase 1 (SERCA1) is one of these genes, and it encodes a P-type ATPase. SERCA1 transports Ca2+ from the cytosol to the lumen, and is involved in muscular relaxation. It has two splice variants (SERCA1a and SERCA1b) that differ in the last eight amino adds, and the contribution of these variants to DM1 pathology is unclear. Here, we show that SERCA1b protein is highly expressed in DM1 muscle tissue, mainly localised at fast twitch fibres. Additionally, when SERCA1a and SERCA1b were overexpressed in cells, we found that the ATPase and Ca2+ uptake activity of SERCA1a was almost double that of SERCA1b. Although the affinity for both ATP and Ca2+ was similar between the two variants, SERCA1b was more sensitive to the inner microsomal environment. Thus, we hypothesise that aberrant expression of SERCA1b in DM1 patients is the cause of abnormal intracellular Ca2+ homeostasis. (C) 2015 Elsevier B.V. All rights reserved.

【 授权许可】

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