High-affinity RNA targets of the Survival Motor Neuron protein reveal diverse preferences for sequence and structural motifs

被引:23
|
作者
Ottesen, Eric W. [1 ]
Singh, Natalia N. [1 ]
Luo, Diou [1 ]
Singh, Ravindra N. [1 ]
机构
[1] Iowa State Univ, Biomed Sci, Ames, IA 50011 USA
基金
美国国家卫生研究院;
关键词
SPINAL MUSCULAR-ATROPHY; ACTIN MESSENGER-RNA; BINDING SPECIFICITY; WIDE IDENTIFICATION; INTRONIC STRUCTURE; GROWTH CONES; SMN COMPLEX; RECOGNITION; CLIP; NEURODEGENERATION;
D O I
10.1093/nar/gky770
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
The Survival Motor Neuron (SMN) protein is essential for survival of all animal cells. SMN harbors a nucleic acid-binding domain and plays an important role in RNA metabolism. However, the RNA-binding property of SMN is poorly understood. Here we employ iterative in vitro selection and chemical structure probing to identify sequence and structural motif(s) critical for RNA-SMN interactions. Our results reveal that motifs that drive RNA-SMN interactions are diverse and suggest that tight RNA-SMN interaction requires presence of multiple contact sites on the RNA molecule. We performed UV crosslinking and immunoprecipitation coupled with high-throughput sequencing (HITS-CLIP) to identify cellular RNA targets of SMN in neuronal SH-SY5Y cells. Results of HITS-CLIP identified a wide variety of targets, including mRNAs coding for ribosome biogenesis and cytoskeleton dynamics. We show critical determinants of ANXA2 mRNA for a direct SMN interaction in vitro. Our data confirms the ability of SMN to discriminate among close RNA sequences, and represent the first validation of a direct interaction of SMN with a cellular RNA target. Our findings suggest direct RNA-SMN interaction as a novel mechanism to initiate the cascade of events leading to the execution of SMN-specific functions.
引用
收藏
页码:10983 / 11001
页数:19
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