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一个与假结兼容的通用位点位于肽基转移酶中心的大核糖体RNA中。

A pseudoknot-compatible universal site is located in the large ribosomal RNA in the peptidyltransferase center.

作者信息

Ivanov V I, Bondarenko S A, Zdobnov E M, Beniaminov A D, Minyat E E, Ulyanov N B

机构信息

Engelhardt Institute of Molecular Biology, Russian Academy of Sciences, Moscow.

出版信息

FEBS Lett. 1999 Mar 5;446(1):60-4. doi: 10.1016/s0014-5793(99)00166-0.

Abstract

The RNA secondary structure is not confined to a system of the hairpins and can contain pseudoknots as well as topologically equivalent slipped-loop structure (SLS) conformations. A specific primary structure that directs folding to the pseudoknot or SLS is called SL-palindrome (SLP). Using a computer program for searching the SLP in the genomic sequences, 419 primary structures of large ribosomal RNAs from different kingdoms (prokaryota, eukaryota, archaebacteria) as well as plastids and mitochondria were analyzed. A universal site was found in the peptidyltransferase center (PTC) capable of folding to a pseudoknot of 48 nucleotides in length. Phylogenetic conservation of its helices (concurrent replacements with no violation of base pairing, covariation) has been demonstrated. We suggest the reversible folding-unfolding of the pseudoknot for certain stages of the ribosome functioning.

摘要

RNA二级结构并不局限于发夹系统,还可以包含假结以及拓扑等价的滑环结构(SLS)构象。一种指导折叠成假结或SLS的特定一级结构被称为SL-回文序列(SLP)。使用一个计算机程序在基因组序列中搜索SLP,分析了来自不同界(原核生物、真核生物、古细菌)以及质体和线粒体的419个大核糖体RNA的一级结构。在肽基转移酶中心(PTC)发现了一个通用位点,它能够折叠成一个长度为48个核苷酸的假结。已经证明了其螺旋的系统发育保守性(在不违反碱基配对的情况下同时替换,共变)。我们认为在核糖体功能的某些阶段假结会发生可逆的折叠-解折叠。

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