Past experiences have demonstrated that available EST data are not strongly associated with RNA editing events and are often misleading-for most coordinates in DARNED, EST data are not available.
#Dj kiran dj g wiki license#
ENSEMBL receives up-to-date date DARNED information through a dedicated Distributed Annotation System (DAS) server ( 42) for all assemblies, see AVAILABILITY AND LICENSE section.
#Dj kiran dj g wiki update#
The DARNED data from the previous update are also directly available in the UCSC browser. The DARNED database is linked to the UCSC Genome Browser ( 40) and ENSEMBL (except for hg18 and mm9 assemblies) ( 41), so that each RNA editing event could be explored in conjunction with annotation tracks within these genome browsers. Preview of sequence-based search results with highlighted known RNA editing locations in the RNA–DNA alignment. Integration of Wikipedia with DARNED through bidirectional hyperlinking is another novel feature of DARNED. Wikipedia was chosen as a platform for this purpose due to its popularity and convenience for community-based annotations ( 38). Inequalities in the functional significance of particular RNA editing events prompted us to start detailed annotation of events whose functions are well-established. In addition to improving DARNED interface, we expanded the database by including RNA editing data from mouse and flies ( 36, 37). We hope that this will stimulate exploration of the true nature of these discrepancies. However, because we cannot exclude a possibility that these events are real, we felt that their inclusion in DARNED is important and appropriate. The absence of plausible mechanisms for RNA editing corresponding to these discrepancies combined with the presence of false positives even in high-confident datasets suggests that corresponding editing events are spurious. Nonetheless, RNA:DNA discrepancies (other than A-to-G and C-to-U) can be found within more confident datasets ( 33–35) which are included into the update. Therefore, these data are not included in the current update of DARNED. This study generated a major controversy, as many follow-up analyses demonstrated that the dataset contains large number of false positives ( 29–32). Recently the existence of all other 10 possible discrepancies between RNA and DNA has also been reported ( 28). In addition to A-to-I editing, a few examples of C-to-U RNA editing (Deamination Cytidine to Uridine) are also well-established in humans ( 26–28). The latter event can generate alternative transcript variants by affecting splice junctions ( 21, 22) or synthesize alternative protein isoforms by non-synonymous codon substitutions in coding regions of mRNA ( 23–25). However, it also occurs in non-repetitive regions and affects sequences of small non-coding RNAs ( 18–20) and pre-mRNAs. sapiens, A-to-I editing dominates in transcripts from the repetitive regions of the genome, especially from Alu elements ( 15–17). Inosine is recognized as Guanosine by ribosomes and reverse transcriptase due to its base pairing with Cytidine ( 14). A-to-I RNA editing (Deamination of Adenosine to Inosine) is the most common type of editing in organisms with a developed central nervous system (CNS) ( 2, 9–13). It is ubiquitous to almost all known life forms ( 2–8). RNA editing results in localized alterations in RNA sequences relative to their genomic templates. The initial release of the database provided access to ∼42 000 coordinates in the human reference genome which have been identified or predicted to undergo RNA editing process upon transcription ( 1).
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