Literature DB >> 15797904

A bioinformatic screen for novel A-I RNA editing sites reveals recoding editing in BC10.

D R Clutterbuck1, A Leroy, M A O'Connell, C A M Semple.   

Abstract

MOTIVATION: Recent studies have demonstrated widespread adenosine-inosine RNA editing in non-coding sequence. However, the extent of editing in coding sequences has remained unknown. For many of the known sites, editing can be observed in multiple species and often occurs in well-conserved sequences. In addition, they often occur within imperfect inverted repeats and in clusters. Here we present a bioinformatic approach to identify novel sites based on these shared features. Mismatches between genomic and expressed sequences were filtered to remove the main sources of false positives, and then prioritized based on these features. This protocol is tailored to identifying specific recoding editing sites, rather than sites in non-coding repeat sequences.
RESULTS: Our protocol is more sensitive for identifying known coding editing sites than any previously published mammalian screen. A novel multiply edited transcript, BC10, was identified and experimentally verified. BC10 is highly conserved across a range of metazoa and has been implicated in two forms of cancer.

Entities:  

Mesh:

Substances:

Year:  2005        PMID: 15797904     DOI: 10.1093/bioinformatics/bti411

Source DB:  PubMed          Journal:  Bioinformatics        ISSN: 1367-4803            Impact factor:   6.937


  32 in total

1.  Extra double-stranded RNA binding domain (dsRBD) in a squid RNA editing enzyme confers resistance to high salt environment.

Authors:  Juan Pablo Palavicini; Rodrigo A Correa-Rojas; Joshua J C Rosenthal
Journal:  J Biol Chem       Date:  2012-03-28       Impact factor: 5.157

2.  Altered RNA editing in mice lacking ADAR2 autoregulation.

Authors:  Yi Feng; Christopher L Sansam; Minati Singh; Ronald B Emeson
Journal:  Mol Cell Biol       Date:  2006-01       Impact factor: 4.272

3.  Dimerization of ADAR2 is mediated by the double-stranded RNA binding domain.

Authors:  Hanne Poulsen; Rasmus Jorgensen; Anders Heding; Finn C Nielsen; Bjarne Bonven; Jan Egebjerg
Journal:  RNA       Date:  2006-05-08       Impact factor: 4.942

4.  An extra double-stranded RNA binding domain confers high activity to a squid RNA editing enzyme.

Authors:  Juan Pablo Palavicini; Mary A O'Connell; Joshua J C Rosenthal
Journal:  RNA       Date:  2009-04-23       Impact factor: 4.942

Review 5.  Letter from the editor: Adenosine-to-inosine RNA editing in Alu repeats in the human genome.

Authors:  Keren Levanon; Eli Eisenberg; Gideon Rechavi; Erez Y Levanon
Journal:  EMBO Rep       Date:  2005-09       Impact factor: 8.807

6.  Hybridization properties of long nucleic acid probes for detection of variable target sequences, and development of a hybridization prediction algorithm.

Authors:  Christina Ohrmalm; Magnus Jobs; Ronnie Eriksson; Sultan Golbob; Amal Elfaitouri; Farid Benachenhou; Maria Strømme; Jonas Blomberg
Journal:  Nucleic Acids Res       Date:  2010-09-22       Impact factor: 16.971

7.  Bladder cancer-associated protein, a potential prognostic biomarker in human bladder cancer.

Authors:  José M A Moreira; Gita Ohlsson; Pavel Gromov; Ronald Simon; Guido Sauter; Julio E Celis; Irina Gromova
Journal:  Mol Cell Proteomics       Date:  2009-09-25       Impact factor: 5.911

8.  RNA editing: a driving force for adaptive evolution?

Authors:  Willemijn M Gommans; Sean P Mullen; Stefan Maas
Journal:  Bioessays       Date:  2009-10       Impact factor: 4.345

Review 9.  Identification of human RNA editing sites: A historical perspective.

Authors:  Gokul Ramaswami; Jin Billy Li
Journal:  Methods       Date:  2016-05-18       Impact factor: 3.608

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

Authors:  Mats Ensterö; Orjan Akerborg; Daniel Lundin; Bei Wang; Terrence S Furey; Marie Ohman; Jens Lagergren
Journal:  BMC Bioinformatics       Date:  2010-01-04       Impact factor: 3.169

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.