Role of the 3' untranslated region in the regulation of cytosolic glutathione peroxidase and phosphlipid-hydroperoxide glutathione peroxidase gene expression by selenium supply

被引:60
作者
Bermano, G [1 ]
Arthur, JR [1 ]
Hesketh, JE [1 ]
机构
[1] ROWETT RES INST,DIV BIOCHEM SCI,ABERDEEN AB21 9SB,SCOTLAND
关键词
D O I
10.1042/bj3200891
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
Selenium is an essential nutrient and synthesis of selenoproteins is affected by limited selenium supply. During selenium deficiency there is a differential regulation of selenoprotein synthesis and gene expression; for example, there is a decrease in abundance of mRNA for cytosolic glutathione peroxidase (cGSH-Px) and a preservation of mRNA for phospholipid-hydroperoxide glutathione peroxidase (PHGSH-Px). This difference is not due to an alteration in the rate of transcription but might reflect differences in translation. The aim of the present work was to assess the role of cGSH-Px and PHGSH-Px 3' untranslated regions (UTRs) in the regulation of selenoprotein mRNA stability and translation by using H4-II-E-C3 cells transfected with different constructs containing a type I iodothyronine deiodinase-coding region linked to different selenoprotein mRNA 3' UTRs. Translational efficiency results showed that the efficiency of the 3' UTRs in permitting selenocysteine incorporation is similar in selenium-replete conditions but, when selenium is limiting, the 3' UTR of cGSH-Px is less efficient than the 3' UTR of PHGSH-Px. The results suggest that the 3' UTR of these selenoprotein mRNA species influences their extent of translation when selenium levels are low. The different sensitivity of the 3' UTRs to selenium deficiency can explain the differential effect that selenium deficiency has on cGSH-Px and PHGSH-Px activity and mRNA levels, stability and translation This might be partly responsible for channelling selenium for synthesis of PHGSH-Px rather than cGSH-Px.
引用
收藏
页码:891 / 895
页数:5
相关论文
共 23 条
  • [1] Arthur J. R., 1994, Selenium in biology and human health., P93
  • [2] HEPATIC IODOTHYRONINE 5'-DEIODINASE - THE ROLE OF SELENIUM
    ARTHUR, JR
    NICOL, F
    BECKETT, GJ
    [J]. BIOCHEMICAL JOURNAL, 1990, 272 (02) : 537 - 540
  • [3] Regulation of selenoprotein gene expression and thyroid hormone metabolism
    Arthur, JR
    Bermano, G
    Mitchell, JH
    Hesketh, JE
    [J]. BIOCHEMICAL SOCIETY TRANSACTIONS, 1996, 24 (02) : 384 - 388
  • [4] TISSUE-SPECIFIC REGULATION OF SELENOENZYME GENE-EXPRESSION DURING SELENIUM DEFICIENCY IN RATS
    BERMANO, G
    NICOL, F
    DYER, JA
    SUNDE, RA
    BECKETT, GJ
    ARTHUR, JR
    HESKETH, JE
    [J]. BIOCHEMICAL JOURNAL, 1995, 311 : 425 - 430
  • [5] Selective control of cytosolic glutathione peroxidase and phospholipid hydroperoxide glutathione peroxidase mRNA stability by selenium supply
    Bermano, G
    Arthur, JR
    Hesketh, JE
    [J]. FEBS LETTERS, 1996, 387 (2-3) : 157 - 160
  • [6] TYPE-I IODOTHYRONINE DEIODINASE IS A SELENOCYSTEINE-CONTAINING ENZYME
    BERRY, MJ
    BANU, L
    LARSEN, PR
    [J]. NATURE, 1991, 349 (6308) : 438 - 440
  • [7] RECOGNITION OF UGA AS A SELENOCYSTEINE CODON IN TYPE-I DEIODINASE REQUIRES SEQUENCES IN THE 3' UNTRANSLATED REGION
    BERRY, MJ
    BANU, L
    CHEN, Y
    MANDEL, SJ
    KIEFFER, JD
    HARNEY, JW
    LARSEN, PR
    [J]. NATURE, 1991, 353 (6341) : 273 - 276
  • [8] BERRY MJ, 1991, J BIOL CHEM, V266, P14156
  • [9] REGULATION OF SELENOPROTEINS
    BURK, RF
    HILL, KE
    [J]. ANNUAL REVIEW OF NUTRITION, 1993, 13 : 65 - 81
  • [10] THE STRUCTURE OF THE MOUSE GLUTATHIONE-PEROXIDASE GENE - THE SELENOCYSTEINE IN THE ACTIVE-SITE IS ENCODED BY THE TERMINATION CODON, TGA
    CHAMBERS, I
    FRAMPTON, J
    GOLDFARB, P
    AFFARA, N
    MCBAIN, W
    HARRISON, PR
    [J]. EMBO JOURNAL, 1986, 5 (06) : 1221 - 1227