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Long 5' leaders inhibit removal of a 3' trailer from a precursor tRNA by mammalian tRNA 3' processing endoribonuclease.

机译:长的5'前导序列通过哺乳动物tRNA 3'加工核糖核酸内切酶抑制从前体tRNA中去除3'尾端。

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摘要

Mammalian tRNA 3' processing endoribonuclease (3' tRNase) can remove a 3' trailer from various pre-tRNAs without 5' leader nucleotides. To examine how 5[prime] leader sequences affect 3' processing efficiency, we performed in vitro 3' processing reactions with purified pig 3' tRNase and pre-tRNAArgs containing a 13-nt 3' trailer and a 5[prime] leader of various lengths. The 3' processing was slightly stimulated by 5[prime] leaders containing up to 7 nt, whereas leaders of 9 nt or longer severely inhibited the reaction. Structure probing indicated that the 5' leader sequences had little effect on pre-tRNA folding. Similar results were obtained using pre-tRNA(Val)s containing a 5' leader of various lengths. We also investigated whether 3'tRNase can remove 3' trailers that are stably base-paired with 5' leaders to form an extended acceptor stem. Even such small 5' leaders as 3 and 6 nt, when base-paired with a 3' trailer, severely hindered removal of the 3' trailer by 3' tRNase.
机译:哺乳动物tRNA 3'加工核糖核酸内切酶(3'tRNase)可以从各种不含5'前导核苷酸的pre-tRNA中去除3'尾部。为了检查5 [prime]前导序列如何影响3'加工效率,我们用纯化的猪3'tRNase和含有13-nt 3'预告片和各种5 [prime]前导的pre-tRNAArgs进行了体外3'处理反应。长度。含有最多7 nt的5 [prime]引导分子会轻微刺激3'的加工,而9 nt或更长的引导分子会严重抑制反应。结构探测表明5'前导序列对pre-tRNA折叠几乎没有影响。使用包含各种长度的5'前导序列的pre-tRNA(Val)获得相似的结果。我们还研究了3'tRNase是否可以去除与5'前导序列碱基稳定配对的3'拖车,从而形成延伸的受体茎。与3'拖车进行碱基配对时,即使3'和6 nt这样小的5'前导分子也严重阻碍了3'tRNase去除3'拖车。

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