» Articles » PMID: 17631420

FSDB: a Frameshift Signal Database

Overview
Publisher Elsevier
Date 2007 Jul 17
PMID 17631420
Citations 10
Authors
Affiliations
Soon will be listed here.
Abstract

Programmed frameshifting is a recoding event in which a ribosome shifts reading frame by one or more nucleotides at a specific mRNA signal between overlapping genes. Programmed frameshifting is involved in the expression of many genes in a wide range of organisms, especially in viruses and bacteria. The mechanism of programmed frameshifting is not fully understood despite many studies, and there are few databases available for detailed information on programmed frameshifting. We have developed a database called FSDB (Frameshift Signal Database), which is a comprehensive compilation of experimentally known or computationally predicted data about programmed ribosomal frameshifting. FSDB provides a graphical view of frameshift signals and the genes using programmed frameshifting for their expression. It also allows the user himself/herself to find programmed frameshift sites in genomic sequences using a program called FSFinder (http://wilab.inha.ac.kr/fsfinder2). We believe FSDB will be a valuable resource for scientists studying programmed ribosomal frameshifting. FSDB is freely accessible at http://wilab.inha.ac.kr/fsdb/.

Citing Articles

PRFect: a tool to predict programmed ribosomal frameshifts in prokaryotic and viral genomes.

McNair K, Salamon P, Edwards R, Segall A BMC Bioinformatics. 2024; 25(1):82.

PMID: 38389044 PMC: 10885494. DOI: 10.1186/s12859-024-05701-0.


Characterization of a Novel Double-Stranded RNA Virus from in New Zealand.

Xu Z, Khalifa M, Frampton R, Smith G, McDougal R, MacDiarmid R Viruses. 2022; 14(2).

PMID: 35215841 PMC: 8878296. DOI: 10.3390/v14020247.


High-throughput interrogation of programmed ribosomal frameshifting in human cells.

Mikl M, Pilpel Y, Segal E Nat Commun. 2020; 11(1):3061.

PMID: 32546731 PMC: 7297798. DOI: 10.1038/s41467-020-16961-8.


RNA-mediated translation regulation in viral genomes: computational advances in the recognition of sequences and structures.

Gupta A, Bansal M Brief Bioinform. 2019; 21(4):1151-1163.

PMID: 31204430 PMC: 7109810. DOI: 10.1093/bib/bbz054.


Ribosomal frameshifting and transcriptional slippage: From genetic steganography and cryptography to adventitious use.

Atkins J, Loughran G, Bhatt P, Firth A, Baranov P Nucleic Acids Res. 2016; 44(15):7007-78.

PMID: 27436286 PMC: 5009743. DOI: 10.1093/nar/gkw530.


References
1.
Moon S, Byun Y, Kim H, Jeong S, Han K . Predicting genes expressed via -1 and +1 frameshifts. Nucleic Acids Res. 2004; 32(16):4884-92. PMC: 519117. DOI: 10.1093/nar/gkh829. View

2.
Ivanov I, Anderson C, Gesteland R, Atkins J . Identification of a new antizyme mRNA +1 frameshifting stimulatory pseudoknot in a subset of diverse invertebrates and its apparent absence in intermediate species. J Mol Biol. 2004; 339(3):495-504. PMC: 7125782. DOI: 10.1016/j.jmb.2004.03.082. View

3.
Byun Y, Han K . PseudoViewer: web application and web service for visualizing RNA pseudoknots and secondary structures. Nucleic Acids Res. 2006; 34(Web Server issue):W416-22. PMC: 1538805. DOI: 10.1093/nar/gkl210. View

4.
Baranov P, Gurvich O, Hammer A, Gesteland R, Atkins J . RECODE 2003. Nucleic Acids Res. 2003; 31(1):87-9. PMC: 165471. DOI: 10.1093/nar/gkg024. View

5.
Baranov P, Gurvich O, Fayet O, Prere M, Miller W, GESTELAND R . RECODE: a database of frameshifting, bypassing and codon redefinition utilized for gene expression. Nucleic Acids Res. 2000; 29(1):264-7. PMC: 29850. DOI: 10.1093/nar/29.1.264. View