Abstract

BackgroundThe vertebrate globin genes encoding the α- and β-subunits of the tetrameric hemoglobins are clustered at two unlinked loci. The highly conserved linear order of the genes flanking the hemoglobins provides a strong anchor for inferring common ancestry of the globin clusters. In fish, the number of α-β-linked globin genes varies considerably between different sublineages and seems to be related to prevailing physico-chemical conditions. Draft sequences of the Atlantic cod genome enabled us to determine the genomic organization of the globin repertoire in this marine species that copes with fluctuating environments of the temperate and Arctic regions.ResultsThe Atlantic cod genome was shown to contain 14 globin genes, including nine hemoglobin genes organized in two unlinked clusters designated β5-α1-β1-α4 and β3-β4-α2-α3-β2. The diverged cod hemoglobin genes displayed different expression levels in adult fish, and tetrameric hemoglobins with or without a Root effect were predicted. The novel finding of maternally inherited hemoglobin mRNAs is consistent with a potential role played by fish hemoglobins in the non-specific immune response. In silico analysis of the six teleost genomes available showed that the two α-β globin clusters are flanked by paralogs of five duplicated genes, in agreement with the proposed teleost-specific duplication of the ancestral vertebrate globin cluster. Screening the genome of extant urochordate and cephalochordate species for conserved globin-flanking genes revealed linkage of RHBDF1, MPG and ARHGAP17 to globin genes in the tunicate Ciona intestinalis, while these genes together with LCMT are closely positioned in amphioxus (Branchiostoma floridae), but seem to be unlinked to the multiple globin genes identified in this species.ConclusionThe plasticity of Atlantic cod to variable environmental conditions probably involves the expression of multiple globins with potentially different properties. The interspecific difference in number of fish hemoglobin genes contrasts with the highly conserved synteny of the flanking genes. The proximity of globin-flanking genes in the tunicate and amphioxus genomes resembles the RHBDF1-MPG-α-globin-ARHGAP17-LCMT linked genes in man and chicken. We hypothesize that the fusion of the three chordate linkage groups 3, 15 and 17 more than 800 MYA led to the ancestral vertebrate globin cluster during a geological period of increased atmospheric oxygen content.

Highlights

  • The vertebrate globin genes encoding the a- and b-subunits of the tetrameric hemoglobins are clustered at two unlinked loci

  • We identified paralogs of stickleback RHBDF1 (ENSGACG00000 004462), ARHGAP17 (ENSGACG00000009145) and FoxJ1 (ENSGACG00000014879) linked on chromosome 5, which, contains no globin genes, whereas an ARHGAP17 duplicate is coupled to the MC locus in pufferfish (ENSTING00000017988), zebrafish (ENS DARG00000075341) and medaka (ENSORLG00000 009090)

  • The Atlantic cod genome was shown to harbor altogether nine a- and b-globin genes organized in two unlinked clusters similar to the other teleost genomes available

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Summary

Introduction

The vertebrate globin genes encoding the a- and b-subunits of the tetrameric hemoglobins are clustered at two unlinked loci. The highly conserved linear order of the genes flanking the hemoglobins provides a strong anchor for inferring common ancestry of the globin clusters. Gnathostomes, the hemoglobin tetramer consists of two pairs of a- and bglobins, which probably arose by duplication of a single primordial globin gene about 500-570 million years ago (MYA) [1,2]. Based on the conservation of the globin-flanking genes, including MPG and c16orf, all gnathostomes examined share a common globin cluster referred to as the MC locus [5] corresponding to the a-globin cluster in placental mammals and chicken. The teleost-specific genome duplication event 350-400 MYA probably gave rise to the second fish a-b globin cluster flanked by ARHGAP17, LCMT and AQP8 [5,8]. The amniotic b-globin cluster is thought to have originated from the transposition of a b gene copy into a region of olfactory receptor genes in their ancestor [8,9,10]

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