Abstract

Coordinated regulation of apoptosis is critical for development, homeostasis, and immunity in larvae of Metazoa. We determined the full nucleotide sequence of an inhibitor of an apoptosis protein in a lepidopteran insect Mythimna separata (Walker) (MsIAP) and carried out functional analyses of the MsIAP. The full-length cDNA of MsIAP was 1642 bp, which encoded 379 amino acid residues with a calculated molecular mass of 41,834 Da, and two BIR domains and one RING domain revealed using amino acid sequence analysis. In addition, the sequences of these domains were similar to Drosophila IAP1 and those of some other lepidopteran insects. We carried out a functional analyses of MsIAP related to apoptosis regulation using RNA interference. The effects of MsIAP knockdown on adhering hemocytes and non-adhering hemocytes as controls were examined using Hoechst33342/propidium iodide staining, effector caspase activity and terminal deoxynucleotidyl transferase-mediated dUTP nick-end labelling (TUNEL) staining. A significantly higher number of propidium iodide and TUNEL-positive cells was recorded in adhering hemocytes from MsIAP knockdown larvae than from control larvae, but these differences were not recorded for non-adhering hemocytes. However, higher effector caspase activity was detected in both adhering and non-adhering hemocytes from MsIAP knockdown larvae compared to that in control larvae. These results indicate that the knockdown of MsIAP induces apoptosis in larval adhering hemocytes, which MsIAP negatively and non-redundantly regulate apoptosis, and that IAP function is conserved in M. separata and other insect species including Drosophila and several lepidopteran insects.

Highlights

  • Apoptosis is a genetically programmed cellular process that removes unwanted, damaged, or infected cells by inducing “suicide” in these cells (Clarke, 1990)

  • We investigated whether the function of an IAP orthologue in the lepidopteran insect, Mythimna separata (Walker) (MsIAP), is conserved

  • Using a partial sequence of MsIAP, we found that MsIAP mRNA was ubiquitously expressed and that significant gene silencing of MsIAP was achieved only in adhering hemocytes from isolated abdomens treated with MsIAP double-stranded RNA

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Summary

Introduction

Apoptosis is a genetically programmed cellular process that removes unwanted, damaged, or infected cells by inducing “suicide” in these cells (Clarke, 1990). The molecular mechanism of apoptosis was initially investigated in the model nematode Caenorhabditis elegans (Maupas), which has a protease ced-3 and nuclease nuc-1 that function as positive and negative regulators of apoptosis, respectively (Horvitz, 2003; Riedl & Shi, 2004). Drosophila melanogaster (Meigen) and mammals have more complex cell death mechanisms. Multiple family ced-3 protease homologs, which are known as caspases, have central roles in regulating apoptosis. During the cell death process, a series of morphologically recognizable changes, such as cell shrinkage, chromatin condensation, genomic DNA fragmentation, membrane blebbing and the emergence of apoptotic bodies, occur (Wyllie et al, 1980)

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