Using phylogenetically-informed annotation (PIA) to search for light-interacting genes in transcriptomes from non-model organisms
Metadata
Show full item recordAuthor/Creator
Date
2014-11-19Type of Work
12 pagesText
journal articles
Citation of Original Publication
Daniel I Speiser, M Sabrina Pankey, Alexander K Zaharoff, Barbara A Battelle, et.al, Using phylogenetically-informed annotation (PIA) to search for light-interacting genes in transcriptomes from non-model organisms, BMC Bioinformatics, 2014,15:350, https://doi.org/10.1186/s12859-014-0350-xRights
This item is likely protected under Title 17 of the U.S. Copyright Law. Unless on a Creative Commons license, for uses protected by Copyright Law, contact the copyright holder or the author.Attribution 4.0 International (CC BY 4.0)
https://creativecommons.org/licenses/by/4.0/
Subjects
bioinformaticseyes
evolution
galaxy
next- generation sequence analysis
orthology
phototransduction
transcriptomes
vision
Abstract
Background: Tools for high throughput sequencing and de novo assembly make the analysis of transcriptomes
(i.e. the suite of genes expressed in a tissue) feasible for almost any organism. Yet a challenge for biologists is that it
can be difficult to assign identities to gene sequences, especially from non-model organisms. Phylogenetic analyses
are one useful method for assigning identities to these sequences, but such methods tend to be time-consuming
because of the need to re-calculate trees for every gene of interest and each time a new data set is analyzed. In
response, we employed existing tools for phylogenetic analysis to produce a computationally efficient, tree-based
approach for annotating transcriptomes or new genomes that we term Phylogenetically-Informed Annotation (PIA),
which places uncharacterized genes into pre-calculated phylogenies of gene families.
Results: We generated maximum likelihood trees for 109 genes from a Light Interaction Toolkit (LIT), a collection of
genes that underlie the function or development of light-interacting structures in metazoans. To do so, we searched
protein sequences predicted from 29 fully-sequenced genomes and built trees using tools for phylogenetic analysis
in the Osiris package of Galaxy (an open-source workflow management system). Next, to rapidly annotate transcriptomes
from organisms that lack sequenced genomes, we repurposed a maximum likelihood-based Evolutionary Placement
Algorithm (implemented in RAxML) to place sequences of potential LIT genes on to our pre-calculated gene trees.
Finally, we implemented PIA in Galaxy and used it to search for LIT genes in 28 newly-sequenced transcriptomes from
the light-interacting tissues of a range of cephalopod mollusks, arthropods, and cubozoan cnidarians. Our new trees for
LIT genes are available on the Bitbucket public repository (http://bitbucket.org/osiris_phylogenetics/pia/) and we
demonstrate PIA on a publicly-accessible web server (http://galaxy-dev.cnsi.ucsb.edu/pia/).
Conclusions: Our new trees for LIT genes will be a valuable resource for researchers studying the evolution of eyes or
other light-interacting structures. We also introduce PIA, a high throughput method for using phylogenetic relationships
to identify LIT genes in transcriptomes from non-model organisms. With simple modifications, our methods may be
used to search for different sets of genes or to annotate data sets from taxa outside of Metazoa.
The following license files are associated with this item:
- Creative Commons