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I组内含子RNA中环化位点的选择需要对内部模板样序列进行多重比对。

Selection of circularization sites in a group I IVS RNA requires multiple alignments of an internal template-like sequence.

作者信息

Been M D, Cech T R

出版信息

Cell. 1987 Sep 11;50(6):951-61. doi: 10.1016/0092-8674(87)90522-8.

Abstract

Circularization and reverse circularization of the Tetrahymena thermophila rRNA intervening sequence resemble the first and second steps in splicing, respectively. However, site-specific base substitutions show that different nucleotides are involved in selection of the 5' splice site and the circularization sites. Furthermore, a substitution at the major circularization site that prevents circularization can be suppressed by second substitutions at two different nucleotide positions. A model is proposed in which adjacent and overlapping sequences can function as a binding site, forming a short duplex with the sequence at the circularization site and thus directing circularization and reverse circularization. Because the 5' exon-binding site and three potential circularization binding sites fall within a contiguous eight nucleotide region, this sequence may translocate relative to the catalytic core of the ribozyme in a template-like manner.

摘要

嗜热四膜虫rRNA间隔序列的环化和反向环化分别类似于剪接的第一步和第二步。然而,位点特异性碱基替换表明,5'剪接位点和环化位点的选择涉及不同的核苷酸。此外,主要环化位点处阻止环化的替换可被两个不同核苷酸位置的第二次替换所抑制。提出了一个模型,其中相邻和重叠序列可作为结合位点,与环化位点处的序列形成短双链体,从而指导环化和反向环化。由于5'外显子结合位点和三个潜在的环化结合位点位于连续的八个核苷酸区域内,该序列可能以模板样方式相对于核酶的催化核心发生易位。

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