Detection of Alternative Splice Variants at the Proteome Level in Aspergillus flavus

dc.contributor.author

Chang, Kung-Yen

dc.contributor.author

Georgianna, D Ryan

dc.contributor.author

Heber, Steffen

dc.contributor.author

Payne, Gary A

dc.contributor.author

Muddiman, David C

dc.date.accessioned

2011-06-21T17:27:12Z

dc.date.available

2011-06-21T17:27:12Z

dc.date.issued

2010

dc.description.abstract

Identification of proteins from proteolytic peptides or intact proteins plays an essential role in proteomics. Researchers use search engines to match the acquired peptide sequences to the target proteins. However, search engines depend on protein databases to provide candidates for consideration. Alternative splicing (AS), the mechanism where the exon of pre-mRNAs can be spliced and rearranged to generate distinct mRNA and therefore protein variants, enable higher eukaryotic organisms, with only a limited number of genes, to have the requisite complexity and diversity at the proteome level. Multiple alternative isoforms from one gene often share common segments of sequences. However, many protein databases only include a limited number of isoforms to keep minimal redundancy. As a result, the database search might not identify a target protein even with high quality tandem MS data and accurate intact precursor ion mass. We computationally predicted an exhaustive list of putative isoforms of Aspergillus flavus proteins from 20 371 expressed sequence tags to investigate whether an alternative splicing protein database can assign a greater proportion of mass spectrometry data. The newly constructed AS database provided 9807 new alternatively spliced variants in addition to 12 832 previously annotated proteins. The searches of the existing tandem MS spectra data set using the AS database identified 29 new proteins encoded by 26 genes. Nine fungal genes appeared to have multiple protein isoforms. In addition to the discovery of splice variants, AS database also showed potential to improve genome annotation. In summary, the introduction of an alternative splicing database helps identify more proteins and unveils more information about a proteome.

dc.description.version

Version of Record

dc.identifier.citation

Chang,Kung-Yen;Georgianna,D. Ryan;Heber,Steffen;Payne,Gary A.;Muddiman,David C.. 2010. Detection of Alternative Splice Variants at the Proteome Level in Aspergillus flavus. Journal of Proteome Research 9(3): 1209-1217.

dc.identifier.issn

1535-3893

dc.identifier.uri

https://hdl.handle.net/10161/4113

dc.language.iso

en_US

dc.publisher

American Chemical Society (ACS)

dc.relation.isversionof

10.1021/pr900602d

dc.relation.journal

Journal of Proteome Research

dc.subject

mass spectrometry

dc.subject

proteomics

dc.subject

alternative splicing

dc.subject

database

dc.subject

aspergillus flavus

dc.subject

cystathionine beta-synthase

dc.subject

tandem mass-spectrometry

dc.subject

identification

dc.subject

gene

dc.subject

sequence

dc.subject

genome

dc.subject

proteins

dc.subject

peptides

dc.subject

polymorphisms

dc.subject

biochemical research methods

dc.title

Detection of Alternative Splice Variants at the Proteome Level in Aspergillus flavus

dc.title.alternative
dc.type

Other article

duke.date.pubdate

2010-3-0

duke.description.issue

3

duke.description.volume

9

pubs.begin-page

1209

pubs.end-page

1217

Files

Original bundle

Now showing 1 - 1 of 1
Loading...
Thumbnail Image
Name:
275088100004.pdf
Size:
1.85 MB
Format:
Adobe Portable Document Format