Chan Russell T, Keating Kevin S, Go Michaela C, Toor Navtej
Department of Chemistry and Biochemistry, University of California, San Diego, La Jolla, CA, 92093, USA.
Schrödinger, LLC, New York, NY, 10036, USA.
J Mol Biol. 2016 Dec 4;428(24 Pt B):4882-4889. doi: 10.1016/j.jmb.2016.10.015. Epub 2016 Oct 19.
Large RNAs often utilize GNRA tetraloops as structural elements to stabilize the overall tertiary fold. These tetraloop-receptor (TR) interactions have a conserved geometry in which the tetraloop docks into the receptor at an angle of ~15° from the helix containing the receptor. Here, we show that the conserved GUAAY pentaloop found in domain III of group IIB1 introns participates in a novel class of RNA tertiary interaction with a geometry and mode of binding that are significantly different from that found in GNRA TR interactions. This pentaloop is highly conserved within the IIB1 class and interacts with the minor groove of the catalytic domain V. The base planes of the loop and receptor nucleotides are not coplanar and greatly deviate from standard A-minor motifs. The helical axis of the GUAAY stem loop diverges ~70° from the angle of insertion found in a typical GNRA TR interaction. Therefore, the loop architecture and insertion orientation are distinctive, with in vitro splicing data indicating that a GNRA tetraloop is incompatible at this position. The GUAAY pentaloop-receptor motif is also found in the structure of the eukaryotic thiamine pyrophosphate riboswitch in the context of a hexanucleotide loop sequence. We therefore propose, based on phylogenetic, structural, and biochemical data, that the GUAAY pentaloop-receptor interaction represents a novel structural motif that is present in multiple structured RNAs.
大的RNA常常利用GNRA四环作为结构元件来稳定整体三级折叠。这些四环-受体(TR)相互作用具有保守的几何结构,其中四环以与包含受体的螺旋呈约15°的角度对接至受体。在此,我们表明在IIB1组内含子的结构域III中发现的保守的GUAAY五环参与了一类新型的RNA三级相互作用,其几何结构和结合模式与GNRA TR相互作用中的显著不同。该五环在IIB1类中高度保守,并与催化结构域V的小沟相互作用。环和受体核苷酸的碱基平面不共面,且与标准的A-小基序有很大偏差。GUAAY茎环的螺旋轴与典型GNRA TR相互作用中的插入角度偏离约70°。因此,环结构和插入方向是独特的,体外剪接数据表明在该位置GNRA四环是不相容的。在六核苷酸环序列的背景下,在真核硫胺焦磷酸核糖开关的结构中也发现了GUAAY五环-受体基序。因此,基于系统发育、结构和生化数据,我们提出GUAAY五环-受体相互作用代表了一种存在于多种结构化RNA中的新型结构基序。