کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
1904587 1534642 2015 6 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Functional analysis of SERCA1b, a highly expressed SERCA1 variant in myotonic dystrophy type 1 muscle
موضوعات مرتبط
علوم زیستی و بیوفناوری بیوشیمی، ژنتیک و زیست شناسی مولکولی سالمندی
پیش نمایش صفحه اول مقاله
Functional analysis of SERCA1b, a highly expressed SERCA1 variant in myotonic dystrophy type 1 muscle
چکیده انگلیسی


• SERCA1b is aberrantly expressed in DM1 muscles.
• SERCA1b has almost half ATPase and Ca2 + uptake activities compared with SERCA1a.
• The lower activity of SERCA1b is due to a high inner microsomal Ca2 + concentration.

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 acids, 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.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease - Volume 1852, Issue 10, Part A, October 2015, Pages 2042–2047
نویسندگان
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