Chavatte L, Frolova L, Kisselev L, Favre A
Institut Jacques Monod, UMR 7592 CNRS-Universités Paris 7-Paris 6, France.
Eur J Biochem. 2001 May;268(10):2896-904. doi: 10.1046/j.1432-1327.2001.02177.x.
It has been shown previously [Brown, C.M. & Tate, W.P. (1994) J. Biol. Chem. 269, 33164-33170.] that the polypeptide chain release factor RF2 involved in translation termination in prokaryotes was able to photocrossreact with mini-messenger RNAs containing stop signals in which U was replaced by 4-thiouridine (s4U). Here, using the same strategy we have monitored photocrosslinking to eukaryotic ribosomal components of 14-mer mRNA in the presence of tRNA(f)(Met), and 42-mer mRNA in the presence of tRNA(Asp) (tRNA(Asp) gene transcript). We show that: (a) both 14-mer and 42-mer mRNAs crossreact with ribosomal RNA and ribosomal proteins. The patterns of the crosslinked ribosomal proteins are similar with both mRNAs and sensitive to ionic conditions; (b) the crosslinking patterns obtained with 42-mer mRNAs show characteristic modification upon addition of tRNA(Asp) providing evidence for appropriate mRNA phasing onto the ribosome. Similar changes are not detected with the 14-mer mRNA.tRNA(f)(Met) pairs; (c) when eukaryotic polypeptide chain release factor 1 (eRF1) is added to the ribosome.tRNA(Asp) complex it crossreacts with the 42-mer mRNA containing the s(4)UGA stop codon located in the A site, but not with the s(4)UCA sense codon; this crosslink involves the N-terminal and middle domains of eRF1 but not the C domain which interacts with eukaryotic polypeptide chain release factor 3 (eRF3); (d) addition of eRF3 has no effect on the yield of eRF1-42-mer mRNA crosslinking and eRF3 does not crossreact with 42-mer mRNA. These experiments delineate the in vitro conditions allowing optimal phasing of mRNA on the eukaryotic ribosome and demonstrate a direct and specific contact of 'core' eRF1 and s(4)UGA stop codon within the ribosomal A site.
先前已表明[布朗,C.M. 及泰特,W.P.(1994年)《生物化学杂志》269卷,33164 - 33170页],参与原核生物翻译终止的多肽链释放因子RF2能够与含有终止信号(其中U被4 - 硫尿苷(s4U)取代)的微型信使RNA进行光交联反应。在此,我们采用相同策略,在甲硫氨酸起始转运RNA(tRNA(f)(Met))存在的情况下监测了14聚体信使RNA与真核核糖体组分的光交联反应,以及在天冬氨酸转运RNA(tRNA(Asp))(tRNA(Asp)基因转录本)存在的情况下监测了42聚体信使RNA与真核核糖体组分的光交联反应。我们发现:(a)14聚体和42聚体信使RNA均与核糖体RNA和核糖体蛋白发生交联反应。两种信使RNA的交联核糖体蛋白模式相似,且对离子条件敏感;(b)在添加tRNA(Asp)后,42聚体信使RNA获得的交联模式呈现出特征性变化,这为信使RNA在核糖体上的正确相位提供了证据。14聚体信使RNA与tRNA(f)(Met)的组合未检测到类似变化;(c)当将真核多肽链释放因子1(eRF1)添加到核糖体 - tRNA(Asp)复合物中时,它会与位于A位点、含有s(4)UGA终止密码子的42聚体信使RNA发生交联反应,但不与s(4)UCA有义密码子发生交联反应;这种交联涉及eRF1的N端和中间结构域,而不涉及与真核多肽链释放因子3(eRF3)相互作用的C结构域;(d)添加eRF3对eRF1与42聚体信使RNA交联的产量没有影响,且eRF3不与42聚体信使RNA发生交联反应。这些实验描绘了使信使RNA在真核核糖体上实现最佳相位的体外条件,并证明了“核心”eRF1与核糖体A位点内的s(4)UGA终止密码子之间存在直接且特异性的接触。