- Discovery notes
- Open Access
Phylogenetic analysis reveals wide distribution of globin X
© Dröge and Makałowski; licensee BioMed Central Ltd. 2011
Received: 26 August 2011
Accepted: 17 October 2011
Published: 17 October 2011
The vertebrate globin gene repertoire consists of seven members that differ in terms of structure, function and phyletic distribution. While hemoglobin, myoglobin, cytoglobin, and neuroglobin are present in almost all gnathostomes examined so far, other globin genes, like globin X, are much more restricted in their phyletic distribution. Till today, globin X has only been found in teleost fish and Xenopus. Here, we report that globin X is also present in the genomes of the sea lamprey, ghost shark and reptiles. Moreover, the identification of orthologs of globin X in crustacean, insects, platyhelminthes, and hemichordates confirms its ancient origin.
Globins are small heme proteins that bind various external ligands, such as oxygen and nitric oxide, and they are found in all kingdoms of life . Best known are hemoglobin (Hb) and myoglobin (Mb), which have been studied for a long time to understand relationships between protein function and structure. In the past ten years, several new members of the globin gene family were added to the vertebrate's globin gene repertoire. Neuroglobin (Ngb) and cytoglobin (Cygb) are highly conserved and present in all gnathostomes examined till today [2–4]. Other novel globin genes are much more restricted in their phyletic distributions, e.g. globin Y (GbY) has been found in Xenopus, lizards, and platypus while globin E (GbE) is only expressed in the eyes of birds [5–7]. Finally, globin X (GbX) seems to be restricted to the genomes of teleost fish and Xenopus [5, 8]. The physiological functions of these novel globin proteins are unknown, although a species-specific regulation of GbX under hypoxic conditions has been observed [9, 10]. Here, we show that the GbX gene is not just restricted to teleost fish and Xenopus genomes, but is also present in the genomes of sea lamprey, ghost shark, and reptiles. Additionally, several invertebrate orthologs of GbX were detected in crustacean, insects, platyhelminthes, and hemichordates, confirming its ancient origin.
The BLAST algorithms  were employed to search the non-redundant protein database of NCBI, the sequence databases at the GenBank and the genomic sequences of the sea lamprey, the ghost shark, the Burmese python, and the green anole lizard for homologous globin proteins. Corresponding nucleotide sequences were extracted from the genomes and translation start sites and splice sites were predicted using GENSCAN and GeneNet2, respectively, and manually adjusted [12–14]. The ExPASy Molecular Biology Server at the Swiss Institute of Bioinformatics was used for the translation of the putative CDS (http://www.expasy.org). A table with accession numbers of sequences used in the consecutive analyses and a table with CDS sequences of the newly annotated genes are provided in the supplementary materials [see Additional file 1]. The derived sequences were initially aligned using the MUSCLE program and manually refined . The alignment is provided in the supplementary materials [see Additional file 2]. Phylogenetic trees were reconstructed using maximum likelihood and Bayesian approaches. The program package RAxML 7.2.8 [16, 17] was employed for maximum likelihood analyses using the rapid bootstrapping algorithm with 1,000 bootstrap replications. Bayesian analyses were conducted in MrBayes 3.1.2 [18, 19] using default priors. Two simultaneous Metropolis-coupled Markov chain Monte Carlo samplings were performed with one cold and three heated chains that were run for 5,000,000 generations. The trees were sampled every 100th generation and the 'burn in' was set to 25%. For the calculation of the phylogenetic trees, the CIPRES portal was used (CIPRES Web Portal V3.1) . Phylogenetic analyses were based on the WAG  model of amino acid evolution assuming gamma distribution of substitution rates, as suggested by analysis of the alignment with ProtTest3 . The phylogenetic trees were visualized with iTOL .
Similarity searches for putative GbX proteins in the nr protein database of NCBI using GbX of zebrafish as query [GenPept: NP_001012261] resulted in the identification of several homologous invertebrate globin proteins and a partial GbX sequence of the green anole lizard [GenPept: XP_003228427]. A tBLASTn search against several vertebrate genomes revealed that GbX is not restricted to teleost fish and amphibians. The GbX gene is also present in the genomes of green anole lizard, Burmese python, ghost shark, and sea lamprey. While teleost fish possess only one copy of the GbX gene, X. tropicalis may indeed contain two GbX genes . For lizard and python we obtained sequences that each correspond to a single GbX gene. Interestingly, ghost shark and sea lamprey may possess two copies of the GbX gene. The coding regions of fish and amphibian GbX are distributed on five exons. The introns are located at positions B12.2 (i.e. between the second and third base of the 12th codon in globin helix B), G7.0, E10.2 and H10.0 . The putative lizard and python GbX genes consist of four coding exons and were found on chrUn_GL343635 and on several contigs (contig24997472, contig25376860, contig25192522, contig25757037), respectively. We couldn't locate the first coding exon of fish and Xenopus GbX, comprising the N-terminal extension and some part of the globin domain (on average the first 57 amino acids), completely in the lizard and partially in the python genome. Moreover, in python the last coding exon comprising the C-terminal extension of the protein seems to be absent. Interestingly, we were able to identify the first coding exon in the previous assembly of the lizard genome (anoCar1.0). Thus, it is most likely that complete first and last coding exons couldn't be found due to missing sequence data and/or due to miss-assembly. The potential CDSs of lizard and python GbX translate into peptides of 200 and 129 amino acids, respectively. The putative ghost shark and sea lamprey GbX genes consist of five coding exons and are distributed on several scaffolds (AAVX01210948, AAVX0160156, AAVX01601570, AAVX01646770, AAVX01022872, AAVX01385372, AAVX01173359, AAVX01250480) and contigs (contig19308, contig21159, contig11157, contig27503), respectively. The putative cDNAs of ghost shark and sea lamprey GbX translate into peptides of 193 and 222 amino acids, respectively. Interestingly, in both species we found partial sequences of a putative second GbX gene (GbX-2). The partial GbX-2 genes of lamprey and shark reside on contig20413, contig362 and on AAVX01509327, AAVX01477794, respectively. For the sea lamprey coding exons two to four were identified that translate into a peptide of 103 amino acids that is 71% identical and (based on BLOSUM62) 88% similar to the other copy of GbX (GbX-1). For the ghost shark only coding exons two and three were identified that translate into a peptide of 75 amino acids. The GbX-2 peptide of the ghost shark is 67% identical and 83% similar to GbX-1. Since large parts of the putative GbX-2 genes couldn't be found in the genomes, those sequences might represent pseudo-genes. The key residues important in oxygen binding, like the proximal and distal histidines in the E- and F-helix (HisE7, HisF8) and the phenylalanine in the CD region (PheCD1) are strictly conserved in all new annotated GbX proteins.
Our phylogenetic analysis supports the scenario that the GbX gene is a product of a duplication event that predates the divergence between protostomes and deuterostomes [8, 24]. As reported before, we were not able to detect GbX in the genomes of mammals and birds. Thus, it seems that GbX was lost twice in vertebrate evolution. Interestingly, the vertebrate lineages that possess a GbX gene represent ectothermic animals while those who lost the GbX gene are endotherms. This distribution may give some hints towards GbX function. Moreover, it will be interesting to see if the ectothermic crocodiles, which are a sister group of birds, own a GbX gene. Crocodiles possess a four-chambered heart which is a characteristic of endotherms in which higher metabolic rates would select for the perfect separation of blood. This led to the hypothesis that the ancestors of crocodilians and birds were endothermic . It will be intriguing to see if GbX was lost in the lineage leading to birds or if was already lost in stem archosaurs.
Reviewer's report 1: Gáspár Jékely, Max Planck Institute for Developmental Biology, Tübingen, Germany
This paper describes novel globin X genes from several vertebrates and invertebrates. The classification of these genes as globin X is confirmed by molecular phylogeny.
Since some nodes in the phylogeny are not well resolved, and there are some groupings inconsistent with the species tree (e.g. the sequences from the deuterostome Saccoglossus grouping with protostome ones), it would be worth showing the alignments as a separate figure. In the alignment members of other globin families should also be included. This could reveal if the globin X group has some shared sequence signatures, distinguishing them from other globins.
The authors should also comment on the putative amphioxus globin X orthologues described in ref 24. The tree in Figure 1 indicates that the amphioxus genes (BflGb3,12,13,14) represent a distinct class, maybe originating at a separate duplication event, predating bilaterian radiation. BflGb6 is missing from the tree.
Thank you for the insightful comments. Globin sequences are difficult to align, indeed. We agree that in such cases it is useful to provide the alignment, which is now available in phylip format as an additional file 2. The amphioxus globin BflGb6 was excluded from the analysis because no globin domain was detected using the normal mode of SMART. The sequence may be mis-annotated since a part of the globin domain is absent in the current version. Other members of the vertebrate globin gene family were not added to the alignment to improve readability of the tree. Moreover, globin X sequences share only little sequence similarity with other vertebrate globin types. We agree that the amphioxus genes (BflGb3, 12, 13, 14) represent a distinct class derived from a separate duplication event predating bilaterian radiation.
Reviewer's report 2: Arcady Mushegian, Stowers Institute for Medical Research, United States of America
This is an interesting observation of broader-then-expected distribution of globin X among metazoa, and of the possible connection between globin X and ectothermy. It is suitable for publication as a Discovery Note, with perhaps one clarification. How do we know what was the ingroup and what was the outgroup, i.e., what are X and what are non-X? Apparently, these calls were made before tree inference, but in principle, the ultimate orthology assignment can be only done by examination of the phylogenetic tree. I suspect that the answer is that globin X sequences were much closer to each other than to any other globins, and therefore the extent of the family could be defined without tree mapping - but this was not stated in the manuscript.
Thank you for your comment that gives us the opportunity to clarify our methodology. The analysis was conducted without prior expectations. A BLAST search was carried out using vertebrate globin X as query to search for similar sequences in invertebrate species. Subsequently, phylogenetic trees were computed to identify relationships between sequences. Neuroglobin was chosen as an outgroup, because it is assumed that neuroglobin emerged before the split of protostomier and deuterostomier. Moreover, globin X is closer related to neuroglobin than to any other vertebrate globin type with identity values ranging from 26% to 34.6%.
Acknowledgements and Funding
This work has been supported by the Institute of Bioinformatics funds.
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