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胰岛素样生长因子I刺激一种编码14 kDa泛素结合酶的mRNA转录物的降解。

Insulin-like growth factor I stimulates degradation of an mRNA transcript encoding the 14 kDa ubiquitin-conjugating enzyme.

作者信息

Wing S S, Bedard N

机构信息

Department of Medicine, McGill University, Montreal, Quebec, Canada.

出版信息

Biochem J. 1996 Oct 15;319 ( Pt 2)(Pt 2):455-61. doi: 10.1042/bj3190455.

Abstract

Upon fasting, the ubiquitin-dependent proteolytic system is activated in skeletal muscle in parallel with the increases in rates of proteolysis. Levels of mRNA encoding the 14 kDa ubiquitin-conjugating enzyme (E2(14K)), which can catalyse the first irreversible reaction in this pathway, rise and fall in parallel with the rates of proteolysis [Wing and Banville (1994) Am.J. Physiol. 267, E39-E48], indicating that the conjugation of ubiquitin to proteins is a regulated step. To characterize the mechanisms of this regulation, we have examined the effects of insulin, insulin-like growth factor I (IGF-I) and des(1-3) insulin-like growth factor I (DES-IGF-I), which does not bind IGF-binding proteins, on E2(14K) mRNA levels in L6 myotubes. Insulin suppressed levels of E2(14K) mRNA with an IC50 of 4 x 10(-9) M, but had no effects on mRNAs encoding polyubiquitin and proteasome subunits C2 and C8, which, like E2(14K), also increase in skeletal muscle upon fasting. Reduction of E2(14K) mRNA levels was more sensitive to IGF-I with an IC50 of approx. 5 x 10(-10) M. During the incubation of these cells for 12 h there was significant secretion of IGF-I-binding proteins into the medium. DES-IGF-I, which has markedly reduced affinity for these binding proteins, was found to potently reduce E2(14K) mRNA levels with an IC50 of 3 x 10(-11) M. DES-IGF-I did not alter rates of transcription of the E2(14K) gene, but enhanced the rate of degradation of the 1.2 kb mRNA transcript. The half-life of the 1.2 kb transcript was approximately one-third that of the 1.8 kb transcript and can explain the more marked regulation of this transcript observed previously. This indicates that the additional 3' non-coding sequence in the 1.8 kb transcript confers stability. These observations suggest that IGF-I is an important regulator of E2(14K) expression and demonstrate, for the first time, stimulation of degradation of a specific mRNA transcript by this hormone, while overall RNA accumulates.

摘要

禁食时,骨骼肌中泛素依赖性蛋白水解系统被激活,同时蛋白水解速率增加。编码14 kDa泛素结合酶(E2(14K))的mRNA水平与蛋白水解速率同步上升和下降,该酶可催化此途径中的第一个不可逆反应[Wing和Banville(1994年),《美国生理学杂志》267卷,E39 - E48页],表明泛素与蛋白质的结合是一个受调控的步骤。为了阐明这种调控机制,我们研究了胰岛素、胰岛素样生长因子I(IGF - I)和去(1 - 3)胰岛素样生长因子I(DES - IGF - I,其不与IGF结合蛋白结合)对L6肌管中E2(14K) mRNA水平的影响。胰岛素抑制E2(14K) mRNA水平,IC50为4×10(-9) M,但对编码多聚泛素以及蛋白酶体亚基C2和C8的mRNA无影响,这些mRNA与E2(14K)一样,在禁食时骨骼肌中也会增加。E2(14K) mRNA水平的降低对IGF - I更敏感,IC50约为5×10(-10) M。在这些细胞孵育12小时期间,有大量IGF - I结合蛋白分泌到培养基中。DES - IGF - I对这些结合蛋白的亲和力显著降低,被发现能有效降低E2(14K) mRNA水平,IC50为3×10(-11) M。DES - IGF - I并未改变E2(14K)基因的转录速率,但提高了1.2 kb mRNA转录本的降解速率。1.2 kb转录本的半衰期约为1.8 kb转录本的三分之一,这可以解释先前观察到的该转录本受到更显著调控的现象。这表明1.8 kb转录本中额外的3'非编码序列赋予了稳定性。这些观察结果表明IGF - I是E2(14K)表达的重要调节因子,并首次证明了该激素对特定mRNA转录本降解的刺激作用,而总体RNA则积累。

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