4.4 Article

Biochemical Methods To Investigate lncRNA and the Influence of IncRNA:Protein Complexes on Chromatin

Journal

BIOCHEMISTRY
Volume 55, Issue 11, Pages 1615-1630

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.biochem.5b01141

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Funding

  1. Duke University
  2. NIH Predoctoral Training Grant in Biomolecular and Tissue Engineering [T32GM008555]

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Long noncoding RNAs (lncRNAs), defined as non translated transcripts greater than 200 nucleotides in length, are often differentially expressed throughout developmental stages, tissue types, and disease states. The identification, visualization, and suppression/overexpression of these sequences have revealed impacts on a wide range of biological processes, including epigenetic regulation. Biochemical investigations on select systems have revealed striking insight into the biological roles of lncRNAs and lncRNA:protein complexes, which in turn prompt even more unanswered questions. To begin, multiple protein- and RNA-centric technologies have been employed to isolate lncRNA:protein and lncRNA:chromatin complexes. lncRNA interactions with the multi-subunit protein complex PRC2, which acts as a transcriptional silencer, represent some of the few cases where the binding affinity, selectivity, and activity of a lncRNA:protein complex have been investigated. At the same time, recent reports of full-length lncRNA secondary structures suggest the formation of complex structures with multiple independent folding domains and pave the way for more detailed structural investigations and predictions of lncRNA three-dimensional structure. This review will provide an overview of the methods and progress made to date as well as highlight new methods that promise to further inform the molecular recognition, specificity, and function of lncRNAs.

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