Abstract

BackgroundHormones are chemical communication signaling molecules released into the body fluids to stimulate target cells of multicellular organisms. We recently showed that histone deacetylase 1 (HDAC1) plays an important role in juvenile hormone (JH) suppression of metamorphosis in the red flour beetle, Tribolium castaneum. Here, we investigated the function of another class I HDAC member, HDAC3, and show that it is required for the normal development of T. castaneum.ResultsRNA interference-mediated knockdown of the HDAC3 gene affected development resulting in abnormally folded wings in pupae and adults. JH analog, hydroprene, suppressed the expression of HDAC3 in T. castaneum larvae. The knockdown of HDAC3 during the final instar larval stage resulted in an increase in the expression of genes coding for proteins involved in JH action. Sequencing of RNA isolated from larvae injected with dsRNA targeting malE (E. coli gene, control) or HDAC3 followed by differential gene expression analysis identified 148 and 741 differentially expressed genes based on the P-value < 0.01 and four-fold difference, and the P-value < 0.05 and two-fold difference, respectively. Several genes, including those coding for myosin-I heavy chain (Myosin 22), Shaven, and nuclear receptor corepressor 1 were identified as differentially expressed genes in HDAC3 knockdown larvae. An increase in histone H3 acetylation, specifically H3K9, H3K18, and H3K27, was detected in HDAC3 knockdown insects.ConclusionOverall, these data suggest that HDAC3 affects the acetylation levels of histones and influences the expression of genes coding for proteins involved in the regulation of growth, development, and metamorphosis.

Highlights

  • Hormones are chemical communication signaling molecules released into the body fluids to stimulate target cells of multicellular organisms

  • Histone deacetylase 3 (HDAC3) plays a key role in development and metamorphosis HDAC3 is a member of the Arginase/deacetylase superfamily that belongs to class I and is structurally and functionally related to histone deacetylase 1 (HDAC1) and HDAC8

  • The pupae that developed from dsHDAC3 treated larvae are smaller in size than the control larvae treated with dsmalE (Additional file 1, Fig. S2)

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Summary

Introduction

Hormones are chemical communication signaling molecules released into the body fluids to stimulate target cells of multicellular organisms. We recently showed that histone deacetylase 1 (HDAC1) plays an important role in juvenile hormone (JH) suppression of metamorphosis in the red flour beetle, Tribolium castaneum. We investigated the function of another class I HDAC member, HDAC3, and show that it is required for the normal development of T. castaneum. Lysine acetylation is one of the major epigenetic modifications of proteins, which contributes to chromatin remodeling and expression of genes that regulate important biological processes [1]. Lysine acetylation targets large macromolecular complexes responsible for various nuclear and cytoplasmic cellular processes: such as splicing, cell cycle, chromatin remodeling, DNA replication, etc. Class I HDACs are localized in the nucleus, expressed universally, and play essential roles in cell proliferation, whereas class II and IV HDACs have a tissue-specific role [7, 8].

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