Abstract

Insects have long been thought to largely not require hemoglobins, with some notable exceptions like the red hemolymph of chironomid larvae. The tubular, branching network of tracheae in hexapods is traditionally considered sufficient for their respiration. Where hemoglobins do occur sporadically in plants and animals, they are believed to be either convergent, or because they are ancient in origin and their expression is lost in many clades. Our comprehensive analysis of 845 Hexapod transcriptomes, totaling over 38 Gbases, revealed the expression of hemoglobins in all 32 orders of hexapods, including the 29 recognized orders of insects. Discovery and identification of 1333 putative hemoglobins were achieved with target-gene BLAST searches of the NCBI TSA database, verifying functional residues, secondary- and tertiary-structure predictions, and localization predictions based on machine learning. While the majority of these hemoglobins are intracellular, extracellular ones were recovered in 38 species. Gene trees were constructed via multiple-sequence alignments and phylogenetic analyses. These indicate duplication events within insects and a monophyletic grouping of hemoglobins outside other globin clades, for which we propose the term insectahemoglobins. These hemoglobins are phylogenetically adjacent and appear structurally convergent with the clade of chordate myoglobins, cytoglobins, and hemoglobins. Their derivation and co-option from early neuroglobins may explain the widespread nature of hemoglobins in various kingdoms and phyla. These results will guide future work involving genome comparisons to transcriptome results, experimental investigations of gene expression, cell and tissue localization, and gas binding properties, all of which are needed to further illuminate the complex respiratory adaptations in insects.

Highlights

  • The colonization of land by arthropods in the Paleozoic required profound changes in respiration. These animals transitioned from a system of gills and respiratory proteins, like hemocyanins, to breathing air

  • Hemoglobins are well known for their common role in respiration, they have various other roles too, discussed below

  • The objective of our study was an extensive, comparative approach to test if hemoglobins are present in the genome, but more importantly, if they are expressed across all orders of Hexapoda

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Summary

Introduction

The colonization of land by arthropods in the Paleozoic required profound changes in respiration. These animals transitioned from a system of gills and respiratory proteins, like hemocyanins, to breathing air. Hemoglobins are well known for their common role in respiration, they have various other roles too, discussed below. Hemoglobins in Hexapoda proteins of 140–150 aa length, usually comprised of eight 3-over-3 α-helical segments (A-H), with Fe++ that binds O2, CO, NO, and CO2. The amino acid sequences can vary widely among taxa, but to preserve the oxygen-binding properties there are two highly recognizable regions in hemoglobin, comprising the characteristic "globin fold": Phe and His occur at positions CD1 and F8, respectively, and hydrophobic residues occur in each of the α-helical segments [1]. Hemoglobins occur in at least five kingdoms of life and 12 phyla of animals from protists to vertebrates [1], but despite their apparent antiquity their expression among animals is presently known to be sporadic, and absent in most orders and species of the largest radiation, the insects [1,2]

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