A critical role for non-coding RNA GAS5 in growth arrest and rapamycin inhibition in human T-lymphocytes

被引:87
|
作者
Williams, Gwyn T. [1 ,2 ]
Mourtada-Maarabouni, Mirna [1 ,2 ]
Farzaneh, Farzin [3 ]
机构
[1] Keele Univ, Inst Sci & Technol Med, Keele ST5 5BG, Staffs, England
[2] Keele Univ, Sch Life Sci, Keele ST5 5BG, Staffs, England
[3] Kings Coll London, Rayne Inst, Dept Haematol Med, London SE5 9NU, England
基金
英国生物技术与生命科学研究理事会; 英国惠康基金;
关键词
growth arrest-specific transcript 5 (GASS); mammalian target of rapamycin (mTOR); non-coding RNA; rapamycin; small nucleolar RNA (snoRNA); T-cell; EXPRESSION CLONING REVEALS; FUNCTIONAL EXPRESSION; MAMMALIAN TARGET; SNORNA U50; CELL-CYCLE; APOPTOSIS; GENE; MUTATION; PROLIFERATION; VARIANTS;
D O I
10.1042/BST0390482
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
Non-coding RNA GAS5 (growth arrest-specific transcript 5) is a 5'-TOP (5'-terminal oligopyrimidine tract) RNA, whose translation, and consequently also stability, is controlled by the mTOR (mammalian target of rapamycin) pathway. GASS was identified by functional expression cloning and is necessary and sufficient for normal growth arrest in both leukaemic and untransformed human T-lymphocytes. GAS5 is also required for the inhibitory effects of rapamycin and its analogues on T-cells. The striking functional effects of GAS5 may be mediated through the snoRNAs (small nucleolar RNAs) encoded in its introns and/or through the unusual folding of the mRNA itself, which sequesters, and therefore inhibits, the glucocorticoid receptor.
引用
收藏
页码:482 / 486
页数:5
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