Abstract

BackgroundUnlike mammals, zebrafish have a remarkable capacity to regenerate a variety of tissues, including central nervous system tissue. The function of macrophages in tissue regeneration is of great interest, as macrophages respond and participate in the landscape of events that occur following tissue injury in all vertebrate species examined. Understanding macrophage populations in regenerating tissue (such as in zebrafish) may inform strategies that aim to regenerate tissue in humans. We recently published an RNA-seq experiment that identified genes enriched in microglia/macrophages in regenerating zebrafish retinas. Interestingly, a small number of transcripts differentially expressed by retinal microglia/macrophages during retinal regeneration did not have predicted orthologs in human or mouse. We reasoned that at least some of these genes could be functionally important for tissue regeneration, but most of these genes have not been studied experimentally and their functions are largely unknown. To reveal their possible functions, we performed a variety of bioinformatic analyses aimed at identifying the presence of functional protein domains as well as orthologous relationships to other species.ResultsOur analyses identified putative functional domains in predicted proteins for a number of selected genes. For example, we confidently predict kinase function for one gene, cytokine/chemokine function for another, and carbohydrate enzymatic function for a third. Predicted orthologs were identified for some, but not all, genes in species with described regenerative capacity, and functional domains were consistent with identified orthologs. Comparison to other published gene expression datasets suggest that at least some of these genes could be important in regenerative responses in zebrafish and not necessarily in response to microbial infection.ConclusionsThis work reveals previously undescribed putative function of several genes implicated in regulating tissue regeneration. This will inform future work to experimentally determine the function of these genes in vivo, and how these genes may be involved in microglia/macrophage roles in tissue regeneration.

Highlights

  • Unlike mammals, zebrafish have a remarkable capacity to regenerate a variety of tissues, including central nervous system tissue

  • These particular 409 transcripts were considered to be “regeneration associated” because they were enriched in microglia/macrophages isolated from regenerating retinal tissue, but were not found to be enriched in resting/steady-state zebrafish brain microglia in another published study [30, 52]

  • Twelve (12) of these genes did not show predicted orthology to human or mouse genes with this analysis and were selected for further bioinformatic analysis (Table 1, denoted P1-P12 throughout the manuscript). We reasoned that these twelve transcripts could be part of a transcriptional program executed in microglia/macrophages during central nervous system (CNS) regeneration, and could be important in understanding similarities and differences in mammalian vs. zebrafish outcomes following tissue damage

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Summary

Introduction

Zebrafish have a remarkable capacity to regenerate a variety of tissues, including central nervous system tissue. We reasoned that at least some of these genes could be functionally important for tissue regeneration, but most of these genes have not been studied experimentally and their functions are largely unknown To reveal their possible functions, we performed a variety of bioinformatic analyses aimed at identifying the presence of functional protein domains as well as orthologous relationships to other species. Macrophage populations appear to be crucial to tissue regeneration [21,22,23,24,25,26,27,28,29,30], though in the mammalian CNS they appear to instead engage in pathological functions [31,32,33,34,35]

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