Alternative RNA splicing in expression of the glutathione synthetase gene in human cells

被引:10
作者
Uchida, Marie [1 ]
Sugaya, Maki [1 ]
Kanamaru, Taichi [2 ]
Hisatomi, Hisashi [1 ]
机构
[1] Seikei Univ, Lab Cellular & Mol Biochem, Dept Mat & Life Sci, Musashino, Tokyo 1808633, Japan
[2] Kobe Rousai Hosp, Dept Surg, Kobe, Hyogo 6510053, Japan
关键词
Glutathione synthetase; Alternative splicing; Oxidative stress; MISSENSE MUTATIONS; HEMOLYTIC-ANEMIA; MESSENGER-RNA; DEFICIENCY; NONSENSE; DISEASE; 5-OXOPROLINURIA; ERYTHROCYTES; ENHANCERS; RECEPTOR;
D O I
10.1007/s11033-009-9675-3
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Ubiquitous free radical production occurs continuously in cells and tissues. Glutathione is the most abundant mammalian antioxidant, and is synthesized by glutathione synthetase (GSS). Therefore, GSS plays an important role in defending the cell against reactive oxygen species. The expression of GSS has been studied in human cells; however, sequence information about alternative splicing variants of GSS mRNA has not been reported. In the present study, we identified a novel alternative splicing variant (ASV) of the GSS gene in 10 human normal tissues and five human cancer cell lines. The deleted transcript of GSS was characterized by an in-frame deletion of 333 bp, corresponding to the complete loss of exons 4 and 5. Thus this GSS ASV causes protein truncation. We quantified the mRNA of GSS ASV in human normal tissues using real-time PCR. The ASV was detected in colon, kidney, lung, liver, placenta, peripheral blood and uterus, but not in heart, skeletal muscle and spleen tissue. Our results provide a basis for more detailed studies on the regulation of GSS, and for further evaluation of this and other possible roles of GSS. Understanding the regulation of GSS expression is very important for the development of new strategies for controlling the development of GSH-based redox homeostasis.
引用
收藏
页码:2105 / 2109
页数:5
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