Discriminative Prediction of A-To-I RNA Editing Events from DNA Sequence

Autor: Bérengère Valtat, Hindrik Mulder, Jiangming Sun, Pratibha Singh, Yang De Marinis, Peter Osmark, Petter Vikman, Peter Spégel, Annika Bagge
Jazyk: angličtina
Rok vydání: 2016
Předmět:
0301 basic medicine
RNA editing
Adenosine
Molecular biology
lcsh:Medicine
Biochemistry
Machine Learning
chemistry.chemical_compound
Database and Informatics Methods
Mice
Protein structure
Sequencing techniques
Invertebrate Genomics
lcsh:Science
Genetics
Multidisciplinary
Mammalian Genomics
RNA sequencing
Genomics
Animal Models
Genomic Databases
Nucleic acids
Sequence Analysis
Research Article
In silico
Sequence Databases
Mouse Models
Biology
Research and Analysis Methods
DNA sequencing
Deep sequencing
Human Genomics
03 medical and health sciences
Model Organisms
Animals
Humans
Computer Simulation
Biology and life sciences
Base Sequence
Genome
Human

lcsh:R
RNA
Computational Biology
DNA
Genome Analysis
Inosine
030104 developmental biology
Biological Databases
Molecular biology techniques
chemistry
Animal Genomics
lcsh:Q
Human genome
Zdroj: PLoS ONE
PLoS ONE, Vol 11, Iss 10, p e0164962 (2016)
ISSN: 1932-6203
Popis: RNA editing is a post-transcriptional alteration of RNA sequences that, via insertions, deletions or base substitutions, can affect protein structure as well as RNA and protein expression. Recently, it has been suggested that RNA editing may be more frequent than previously thought. A great impediment, however, to a deeper understanding of this process is the paramount sequencing effort that needs to be undertaken to identify RNA editing events. Here, we describe an in silico approach, based on machine learning, that ameliorates this problem. Using 41 nucleotide long DNA sequences, we show that novel A-to-I RNA editing events can be predicted from known A-to-I RNA editing events intra- and interspecies. The validity of the proposed method was verified in an independent experimental dataset. Using our approach, 203 202 putative A-to-I RNA editing events were predicted in the whole human genome. Out of these, 9% were previously reported. The remaining sites require further validation, e.g., by targeted deep sequencing. In conclusion, the approach described here is a useful tool to identify potential A-to-I RNA editing events without the requirement of extensive RNA sequencing.
Databáze: OpenAIRE