lnCeDB: database of human long noncoding RNA acting as competing endogenous RNA.

Long noncoding RNA (lncRNA) influences post-transcriptional regulation by interfering with the microRNA (miRNA) pathways, acting as competing endogenous RNA (ceRNA). These lncRNAs have miRNA responsive elements (MRE) in them, and control endogenous miRNAs available for binding with their target mRNA...

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Main Authors: Shaoli Das, Suman Ghosal, Rituparno Sen, Jayprokas Chakrabarti
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2014-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC4057149?pdf=render
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spelling doaj-6259201fb05b4ab0aa3df25dbe372b942020-11-24T21:50:32ZengPublic Library of Science (PLoS)PLoS ONE1932-62032014-01-0196e9896510.1371/journal.pone.0098965lnCeDB: database of human long noncoding RNA acting as competing endogenous RNA.Shaoli DasSuman GhosalRituparno SenJayprokas ChakrabartiLong noncoding RNA (lncRNA) influences post-transcriptional regulation by interfering with the microRNA (miRNA) pathways, acting as competing endogenous RNA (ceRNA). These lncRNAs have miRNA responsive elements (MRE) in them, and control endogenous miRNAs available for binding with their target mRNAs, thus reducing the repression of these mRNAs. lnCeDB provides a database of human lncRNAs (from GENCODE 19 version) that can potentially act as ceRNAs. The putative mRNA targets of human miRNAs and the targets mapped to AGO clipped regions are collected from TargetScan and StarBase respectively. The lncRNA targets of human miRNAs (up to GENCODE 11) are downloaded from miRCode database. miRNA targets on the rest of the GENCODE 19 lncRNAs are predicted by our algorithm for finding seed-matched target sites. These putative miRNA-lncRNA interactions are mapped to the Ago interacting regions within lncRNAs. To find out the likelihood of an lncRNA-mRNA pair for actually being ceRNA we take recourse to two methods. First, a ceRNA score is calculated from the ratio of the number of shared MREs between the pair with the total number of MREs of the individual candidate gene. Second, the P-value for each ceRNA pair is determined by hypergeometric test using the number of shared miRNAs between the ceRNA pair against the number of miRNAs interacting with the individual RNAs. Typically, in a pair of RNAs being targeted by common miRNA(s), there should be a correlation of expression so that the increase in level of one ceRNA results in the increased level of the other ceRNA. Near-equimolar concentration of the competing RNAs is associated with more profound ceRNA effect. In lnCeDB one can not only browse for lncRNA-mRNA pairs having common targeting miRNAs, but also compare the expression of the pair in 22 human tissues to estimate the chances of the pair for actually being ceRNAs.Downloadable freely from http://gyanxet-beta.com/lncedb/.http://europepmc.org/articles/PMC4057149?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Shaoli Das
Suman Ghosal
Rituparno Sen
Jayprokas Chakrabarti
spellingShingle Shaoli Das
Suman Ghosal
Rituparno Sen
Jayprokas Chakrabarti
lnCeDB: database of human long noncoding RNA acting as competing endogenous RNA.
PLoS ONE
author_facet Shaoli Das
Suman Ghosal
Rituparno Sen
Jayprokas Chakrabarti
author_sort Shaoli Das
title lnCeDB: database of human long noncoding RNA acting as competing endogenous RNA.
title_short lnCeDB: database of human long noncoding RNA acting as competing endogenous RNA.
title_full lnCeDB: database of human long noncoding RNA acting as competing endogenous RNA.
title_fullStr lnCeDB: database of human long noncoding RNA acting as competing endogenous RNA.
title_full_unstemmed lnCeDB: database of human long noncoding RNA acting as competing endogenous RNA.
title_sort lncedb: database of human long noncoding rna acting as competing endogenous rna.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2014-01-01
description Long noncoding RNA (lncRNA) influences post-transcriptional regulation by interfering with the microRNA (miRNA) pathways, acting as competing endogenous RNA (ceRNA). These lncRNAs have miRNA responsive elements (MRE) in them, and control endogenous miRNAs available for binding with their target mRNAs, thus reducing the repression of these mRNAs. lnCeDB provides a database of human lncRNAs (from GENCODE 19 version) that can potentially act as ceRNAs. The putative mRNA targets of human miRNAs and the targets mapped to AGO clipped regions are collected from TargetScan and StarBase respectively. The lncRNA targets of human miRNAs (up to GENCODE 11) are downloaded from miRCode database. miRNA targets on the rest of the GENCODE 19 lncRNAs are predicted by our algorithm for finding seed-matched target sites. These putative miRNA-lncRNA interactions are mapped to the Ago interacting regions within lncRNAs. To find out the likelihood of an lncRNA-mRNA pair for actually being ceRNA we take recourse to two methods. First, a ceRNA score is calculated from the ratio of the number of shared MREs between the pair with the total number of MREs of the individual candidate gene. Second, the P-value for each ceRNA pair is determined by hypergeometric test using the number of shared miRNAs between the ceRNA pair against the number of miRNAs interacting with the individual RNAs. Typically, in a pair of RNAs being targeted by common miRNA(s), there should be a correlation of expression so that the increase in level of one ceRNA results in the increased level of the other ceRNA. Near-equimolar concentration of the competing RNAs is associated with more profound ceRNA effect. In lnCeDB one can not only browse for lncRNA-mRNA pairs having common targeting miRNAs, but also compare the expression of the pair in 22 human tissues to estimate the chances of the pair for actually being ceRNAs.Downloadable freely from http://gyanxet-beta.com/lncedb/.
url http://europepmc.org/articles/PMC4057149?pdf=render
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