New scoring system to identify RNA G-quadruplex folding

被引:97
作者
Beaudoin, Jean-Denis [1 ]
Jodoin, Rachel [1 ]
Perreault, Jean-Pierre [1 ]
机构
[1] Univ Sherbrooke, Pavillon Rech Appl Canc, Fa Med & Sci Sante, RNA Group Groupe ARN,Dept Biochim, Sherbrooke, PQ J1E 4K8, Canada
关键词
REGULATORY MOTIFS; HUMAN GENOME; DNA; STABILITY; SEQUENCES; DEFINITION; PREVALENCE; TOPOLOGY; ROLES;
D O I
10.1093/nar/gkt904
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
G-quadruplexes (G4s) are non-canonical structures involved in many important cellular processes. To date, the prediction of potential G-quadruplex structures (PG4s) has been based almost exclusively on the sequence of interest agreeing with the algorithm G(x)-N-(1-7)-G(x)-N1-7-G(x)-N1-7-G(x) (where x >= 3 and N = A, U, G or C). However, many sequences agreeing with this algorithm do not form G4s and are considered false-positive predictions. Here we show the RNA PG4 candidate in the 3'-untranslated region (UTR) of the TTYH1 gene to be one such false positive. Specifically, G4 folding was observed to be inhibited by the presence of multiple-cytosine tracks, located in the candidate's genomic context, that adopted a Watson-Crick base-paired structure. Clearly, the neighbouring sequences of a PG4 may influence its folding. The secondary structure of 12 PG4 motifs along with either 15 or 50 nucleotides of their upstream and downstream genomic contexts were evaluated by in-line probing. Data permitted the development of a scoring system for the prediction of PG4s taking into account the effect of the neighbouring sequences. The accuracy of this scoring system was assessed by probing 14 other novel PG4 candidates retrieved in human 5'-UTRs. This new scoring system can be used, in combination with the standard algorithm, to better predict the folding of RNA G4s.
引用
收藏
页码:1209 / 1223
页数:15
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