Network-based bioinformatics analysis of spatio-temporal RNA-Seq data reveals transcriptional programs underpinning normal and aberrant retinal development
| Autor: | Christopher Lemoine, Devi Krishna Priya Karunakaran, Abdul Rouf Banday, Ion I. Mandoiu, Sahar Al Seesi, Marybeth Baumgartner, Anouk M. Olthof, Rahul N. Kanadia |
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| Rok vydání: | 2016 |
| Předmět: |
0301 basic medicine
RNA-Seq Computational biology Biology Deep sequencing Retina Transcriptome 03 medical and health sciences Mice Spatio-Temporal Analysis Genetics Animals Gene Mice Knockout Sequence Analysis RNA Gene Expression Profiling Research Alternative splicing Computational Biology Gene expression profiling Alternative Splicing Kinetics 030104 developmental biology Disease Progression DNA microarray Functional genomics Biotechnology |
| Zdroj: | BMC Genomics |
| ISSN: | 1471-2164 |
| Popis: | Background The retina as a model system with extensive information on genes involved in development/maintenance is of great value for investigations employing deep sequencing to capture transcriptome change over time. This in turn could enable us to find patterns in gene expression across time to reveal transition in biological processes. Methods We developed a bioinformatics pipeline to categorize genes based on their differential expression and their alternative splicing status across time by binning genes based on their transcriptional kinetics. Genes within same bins were then leveraged to query gene annotation databases to discover molecular programs employed by the developing retina. Results Using our pipeline on RNA-Seq data obtained from fractionated (nucleus/cytoplasm) developing retina at embryonic day (E) 16 and postnatal day (P) 0, we captured high-resolution as in the difference between the cytoplasm and the nucleus at the same developmental time. We found de novo transcription of genes whose transcripts were exclusively found in the nuclear transcriptome at P0. Further analysis showed that these genes enriched for functions that are known to be executed during postnatal development, thus showing that the P0 nuclear transcriptome is temporally ahead of that of its cytoplasm. We extended our strategy to perform temporal analysis comparing P0 data to either P21-Nrl-wildtype (WT) or P21-Nrl-knockout (KO) retinae, which predicted that the KO retina would have compromised vasculature. Indeed, histological manifestation of vasodilation has been reported at a later time point (P60). Conclusions Thus, our approach was predictive of a phenotype before it presented histologically. Our strategy can be extended to investigating the development and/or disease progression of other tissue types. Electronic supplementary material The online version of this article (doi:10.1186/s12864-016-2822-z) contains supplementary material, which is available to authorized users. |
| Databáze: | OpenAIRE |
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