Functional modelling of an equine bronchoalveolar lavage fluid proteome provides experimental confirmation and functional annotation of equine genome sequences

• Published in: Animal genetics 2011-08, Vol.42 (4), p.395-405
• Main Authors: Bright, L. A., Mujahid, N., Nanduri, B., McCarthy, F. M., Costa, L. R. R., Burgess, S. C., Swiderski, C. E.
• Format: Article
• Language: English
• Subjects: Animals; bronchoalveolar lavage; Bronchoalveolar Lavage Fluid - chemistry; equine; Genes; Genome - genetics; genome annotation; Genomes; Genomics; Horses - genetics; Humans; Mass Spectrometry; Medical research; Mice; Models, Biological; Molecular Sequence Annotation - methods; Proteins; Proteins - analysis; Proteins - genetics; Proteins - physiology; proteomics; Proteomics - methods
• ISSN: 0268-9146; 1365-2052
• DOI: 10.1111/j.1365-2052.2010.02158.x

Summary The equine genome sequence enables the use of high‐throughput genomic technologies in equine research, but accurate identification of expressed gene products and interpreting their biological relevance require additional structural and functional genome annotation. Here, we employ the equine genome sequence to identify predicted and known proteins using proteomics and model these proteins into biological pathways, identifying 582 proteins in normal cell‐free equine bronchoalveolar lavage fluid (BALF). We improved structural and functional annotation by directly confirming the in vivo expression of 558 (96%) proteins, which were computationally predicted previously, and adding Gene Ontology (GO) annotations for 174 proteins, 108 of which lacked functional annotation. Bronchoalveolar lavage is commonly used to investigate equine respiratory disease, leading us to model the associated proteome and its biological functions. Modelling of protein functions using Ingenuity Pathway Analysis identified carbohydrate metabolism, cell‐to‐cell signalling, cellular function, inflammatory response, organ morphology, lipid metabolism and cellular movement as key biological processes in normal equine BALF. Comparative modelling of protein functions in normal cell‐free bronchoalveolar lavage proteomes from horse, human, and mouse, performed by grouping GO terms sharing common ancestor terms, confirms conservation of functions across species. Ninety‐one of 92 human GO categories and 105 of 109 mouse GO categories were conserved in the horse. Our approach confirms the utility of the equine genome sequence to characterize protein networks without antibodies or mRNA quantification, highlights the need for continued structural and functional annotation of the equine genome and provides a framework for equine researchers to aid in the annotation effort.