Sengupta Aniruddha, Carlson Bradley A, Weaver James A, Novoselov Sergey V, Fomenko Dmitri E, Gladyshev Vadim N, Hatfield Dolph L
Molecular Biology of Selenium Section, Laboratory of Cancer Prevention, CCR, NCI, NIH, Bethesda, MD 20892, USA.
Biochem J. 2008 Jul 1;413(1):151-61. doi: 10.1042/BJ20080277.
Sec (selenocysteine) is biosynthesized on its tRNA and incorporated into selenium-containing proteins (selenoproteins) as the 21st amino acid residue. Selenoprotein synthesis is dependent on Sec tRNA and the expression of this class of proteins can be modulated by altering Sec tRNA expression. The gene encoding Sec tRNA (Trsp) is a single-copy gene and its targeted removal in liver demonstrated that selenoproteins are essential for proper function wherein their absence leads to necrosis and hepatocellular degeneration. In the present study, we found that the complete loss of selenoproteins in liver was compensated for by an enhanced expression of several phase II response genes and their corresponding gene products. The replacement of selenoprotein synthesis in mice carrying mutant Trsp transgenes, wherein housekeeping, but not stress-related selenoproteins are expressed, led to normal expression of phase II response genes. Thus the present study provides evidence for a functional link between housekeeping selenoproteins and phase II enzymes.
硒代半胱氨酸(Sec)在其转运RNA(tRNA)上生物合成,并作为第21个氨基酸残基掺入含硒蛋白(硒蛋白)中。硒蛋白的合成依赖于硒代半胱氨酸tRNA,并且这类蛋白质的表达可以通过改变硒代半胱氨酸tRNA的表达来调节。编码硒代半胱氨酸tRNA(Trsp)的基因是单拷贝基因,在肝脏中对其进行靶向敲除表明,硒蛋白对于正常功能至关重要,缺乏它们会导致坏死和肝细胞变性。在本研究中,我们发现肝脏中硒蛋白的完全缺失通过几种II期反应基因及其相应基因产物的表达增强得到了补偿。在携带突变型Trsp转基因的小鼠中,看家硒蛋白而非应激相关硒蛋白得以表达,这替代了硒蛋白的合成,从而导致II期反应基因的正常表达。因此,本研究为看家硒蛋白与II期酶之间的功能联系提供了证据。