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Sökning: onr:"swepub:oai:DiVA.org:kth-19281" > A computational scr...

A computational screen for site selective A-to-I editing detects novel sites in neuron specific Hu proteins

Ensterö, Mats (författare)
Stockholms universitet,Institutionen för molekylärbiologi och funktionsgenomik,Department of Molecular Biology and Functional Genomics, Stockholm University
Åkerborg, Örjan (författare)
Stockholms universitet,KTH,Beräkningsbiologi, CB,Institutionen för biokemi och biofysik,Stockholm University ; KTH Royal Institute of Technology
Lundin, Daniel (författare)
Stockholms universitet,Institutionen för molekylärbiologi och funktionsgenomik,Department of Molecular Biology and Functional Genomics, Stockholm University,Jarone Pinhassi
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Wang, Bei (författare)
Department of Computer Science, Duke University, Durham, United States,Duke University, USA
Furey, Terrence S. (författare)
Department of Computer Science, Duke University, Durham, United States,Institute for Genome Sciences and Policy (IGSP), USA ; Duke University, USA
Öhman, Marie (författare)
Stockholms universitet,Institutionen för molekylärbiologi och funktionsgenomik,Department of Molecular Biology and Functional Genomics, Stockholm University
Lagergren, Jens (författare)
KTH,Beräkningsbiologi, CB,Stockholm University ; KTH Royal Institute of Technology
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 (creator_code:org_t)
2010-01-04
2010
Engelska.
Ingår i: BMC Bioinformatics. - : Springer Science and Business Media LLC. - 1471-2105. ; 11
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Background: Several bioinformatic approaches have previously been used to find novel sites of ADAR mediated A-to-I RNA editing in human. These studies have discovered thousands of genes that are hyper-edited in their non-coding intronic regions, especially in alu retrotransposable elements, but very few substrates that are site-selectively edited in coding regions. Known RNA edited substrates suggest, however, that site selective A-to-I editing is particularly important for normal brain development in mammals. Results: We have compiled a screen that enables the identification of new sites of site-selective editing, primarily in coding sequences. To avoid hyper-edited repeat regions, we applied our screen to the alu-free mouse genome. Focusing on the mouse also facilitated better experimental verification. To identify candidate sites of RNA editing, we first performed an explorative screen based on RNA structure and genomic sequence conservation. We further evaluated the results of the explorative screen by determining which transcripts were enriched for A-G mismatches between the genomic template and the expressed sequence since the editing product, inosine (I), is read as guanosine (G) by the translational machinery. For expressed sequences, we only considered coding regions to focus entirely on re-coding events. Lastly, we refined the results from the explorative screen using a novel scoring scheme based on characteristics for known A-to-I edited sites. The extent of editing in the final candidate genes was verified using total RNA from mouse brain and 454 sequencing. Conclusions: Using this method, we identified and confirmed efficient editing at one site in the Gabra3 gene. Editing was also verified at several other novel sites within candidates predicted to be edited. Five of these sites are situated in genes coding for the neuron-specific RNA binding proteins HuB and HuD.

Ämnesord

NATURVETENSKAP  -- Biologi -- Bioinformatik och systembiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Bioinformatics and Systems Biology (hsv//eng)
NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)

Nyckelord

double-stranded-rna
pre-messenger-rna
adenosine deamination
snp
database
identification
adar1
gene
sequences
mouse
information
Bioinformatics
Bioinformatik
NATURAL SCIENCES
Biochemistry

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