TY - JOUR
T1 - Tertiary Motifs Revealed in Analyses of Higher-Order RNA Junctions
AU - Laing, Christian
AU - Jung, Segun
AU - Iqbal, Abdul
AU - Schlick, Tamar
N1 - Funding Information:
This work was supported by the Human Frontier Science Program, by a joint National Science Foundation (NSF)/National Institute of General Medical Sciences initiative in Mathematical Biology (DMS-0201160), and by NSF EMT award # CF-0727001. Partial support by the National Institutes of Health (grant # R01-GM055164 and grant # 1 R01 ES 012692) and NSF (grant # CCF-0727001) is also gratefully acknowledged. A.I. was supported by the New York University Dean's Undergraduate Research Fund FAS Frances and Benjamin Benenson Research Scholar, and S.J. was supported by the Sackler Institute Biomedical Science Training Fellowship and a MacCracken Fellowship.
PY - 2009/10/16
Y1 - 2009/10/16
N2 - RNA junctions are secondary-structure elements formed when three or more helices come together. They are present in diverse RNA molecules with various fundamental functions in the cell. To better understand the intricate architecture of three-dimensional (3D) RNAs, we analyze currently solved 3D RNA junctions in terms of base-pair interactions and 3D configurations. First, we study base-pair interaction diagrams for solved RNA junctions with 5 to 10 helices and discuss common features. Second, we compare these higher-order junctions to those containing 3 or 4 helices and identify global motif patterns such as coaxial stacking and parallel and perpendicular helical configurations. These analyses show that higher-order junctions organize their helical components in parallel and helical configurations similar to lower-order junctions. Their sub-junctions also resemble local helical configurations found in three- and four-way junctions and are stabilized by similar long-range interaction preferences such as A-minor interactions. Furthermore, loop regions within junctions are high in adenine but low in cytosine, and in agreement with previous studies, we suggest that coaxial stacking between helices likely forms when the common single-stranded loop is small in size; however, other factors such as stacking interactions involving noncanonical base pairs and proteins can greatly determine or disrupt coaxial stacking. Finally, we introduce the ribo-base interactions: when combined with the along-groove packing motif, these ribo-base interactions form novel motifs involved in perpendicular helix-helix interactions. Overall, these analyses suggest recurrent tertiary motifs that stabilize junction architecture, pack helices, and help form helical configurations that occur as sub-elements of larger junction networks. The frequent occurrence of similar helical motifs suggest nature's finite and perhaps limited repertoire of RNA helical conformation preferences. More generally, studies of RNA junctions and tertiary building blocks can ultimately help in the difficult task of RNA 3D structure prediction.
AB - RNA junctions are secondary-structure elements formed when three or more helices come together. They are present in diverse RNA molecules with various fundamental functions in the cell. To better understand the intricate architecture of three-dimensional (3D) RNAs, we analyze currently solved 3D RNA junctions in terms of base-pair interactions and 3D configurations. First, we study base-pair interaction diagrams for solved RNA junctions with 5 to 10 helices and discuss common features. Second, we compare these higher-order junctions to those containing 3 or 4 helices and identify global motif patterns such as coaxial stacking and parallel and perpendicular helical configurations. These analyses show that higher-order junctions organize their helical components in parallel and helical configurations similar to lower-order junctions. Their sub-junctions also resemble local helical configurations found in three- and four-way junctions and are stabilized by similar long-range interaction preferences such as A-minor interactions. Furthermore, loop regions within junctions are high in adenine but low in cytosine, and in agreement with previous studies, we suggest that coaxial stacking between helices likely forms when the common single-stranded loop is small in size; however, other factors such as stacking interactions involving noncanonical base pairs and proteins can greatly determine or disrupt coaxial stacking. Finally, we introduce the ribo-base interactions: when combined with the along-groove packing motif, these ribo-base interactions form novel motifs involved in perpendicular helix-helix interactions. Overall, these analyses suggest recurrent tertiary motifs that stabilize junction architecture, pack helices, and help form helical configurations that occur as sub-elements of larger junction networks. The frequent occurrence of similar helical motifs suggest nature's finite and perhaps limited repertoire of RNA helical conformation preferences. More generally, studies of RNA junctions and tertiary building blocks can ultimately help in the difficult task of RNA 3D structure prediction.
KW - RNA structure
KW - junction
KW - non-Watson-Crick base pair
KW - ribo-base interaction
KW - tertiary motif
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U2 - 10.1016/j.jmb.2009.07.089
DO - 10.1016/j.jmb.2009.07.089
M3 - Article
C2 - 19660472
AN - SCOPUS:70349238567
SN - 0022-2836
VL - 393
SP - 67
EP - 82
JO - Journal of Molecular Biology
JF - Journal of Molecular Biology
IS - 1
ER -