Abstract

Crucian carp are unusual among vertebrates in surviving extended periods in the complete absence of molecular oxygen. During this time cardiac output is maintained though these mechanisms are not well understood. Using a high-density cDNA microarray, we have defined the genome-wide gene expression responses of cardiac tissue after exposing the fish at two temperatures (8 and 13°C) to one and seven days of anoxia, followed by seven days after restoration to normoxia. At 8°C, using a false discovery rate of 5%, neither anoxia nor re-oxygenation elicited appreciable changes in gene expression. By contrast, at 13°C, 777 unique genes responded strongly. Up-regulated genes included those involved in protein turnover, the pentose phosphate pathway and cell morphogenesis while down-regulated gene categories included RNA splicing and transcription. Most genes were affected between one and seven days of anoxia, indicating gene regulation over the medium term but with few early response genes. Re-oxygenation for 7 days was sufficient to completely reverse these responses. Glycolysis displayed more complex responses with anoxia up-regulated transcripts for the key regulatory enzymes, hexokinase and phosphofructokinase, but with down-regulation of most of the non-regulatory genes. This complex pattern of responses in genomic transcription patterns indicates divergent cardiac responses to anoxia, with the transcriptionally driven reprogramming of cardiac function seen at 13°C being largely completed at 8°C.

Highlights

  • Vertebrates in general are highly dependent on aerobic metabolism and most suffer profound negative effects of environmental or tissue hypoxia

  • Gene expression profiles following anoxia treatment We contrasted the treatment groups using the design shown in Figure 1 based on a series of comparisons using two-colour arrays

  • Based on a FDR of,5% we identified 777 unique genes that showed changes in transcript abundance between normoxia and anoxia at 13uC, and a near complete reversal following an additional seven days under normoxia

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Summary

Introduction

Vertebrates in general are highly dependent on aerobic metabolism and most suffer profound negative effects of environmental or tissue hypoxia. In contrast to mammalian hearts, cardiac activity in carp is fully maintained during prolonged anoxia [7] to sustain blood transport of glucose to fuel glycolysis in all tissues, of lactate to skeletal muscle, and of ethanol to the gills [8]. The lack of detrimental effects of anoxia exposure on the crucian carp heart contrasts with mammalian hearts, which show extensive and irreversible injury including myocyte cell death following interruption of blood flow (ischemia) and after the subsequent reperfusion [9]. This makes the anoxic crucian carp heart a interesting model to understand how evolution has solved the problem of anoxic survival

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