| Autor: |
Piro RM; Institut für Informatik, Freie Universität Berlin, Berlin, Germany.; Institut für Medizinische Genetik und Humangenetik, Charité-Universitätsmedizin Berlin, Berlin, Germany., Marsico A; Institut für Informatik, Freie Universität Berlin, Berlin, Germany. marsico@molgen.mpg.de.; Max-Planck-Institut für molekulare Genetik, Berlin, Germany. marsico@molgen.mpg.de. |
| Jazyk: |
angličtina |
| Zdroj: |
Methods in molecular biology (Clifton, N.J.) [Methods Mol Biol] 2019; Vol. 1912, pp. 301-321. |
| DOI: |
10.1007/978-1-4939-8982-9_12 |
| Abstrakt: |
The discovery that a considerable portion of eukaryotic genomes is transcribed and gives rise to long noncoding RNAs (lncRNAs) provides an important new perspective on the transcriptome and raises questions about the centrality of these lncRNAs in gene-regulatory processes and diseases. The rapidly increasing number of mechanistically investigated lncRNAs has provided evidence for distinct functional classes, such as enhancer-like lncRNAs, which modulate gene expression via chromatin looping, and noncoding competing endogenous RNAs (ceRNAs), which act as microRNA decoys. Despite great progress in the last years, the majority of lncRNAs are functionally uncharacterized and their implication for disease biogenesis and progression is unknown. Here, we summarize recent developments in lncRNA function prediction in general and lncRNA-disease associations in particular, with emphasis on in silico methods based on network analysis and on ceRNA function prediction. We believe that such computational techniques provide a valuable aid to prioritize functional lncRNAs or disease-relevant lncRNAs for targeted, experimental follow-up studies. |
| Databáze: |
MEDLINE |
| Externí odkaz: |
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