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Oellermann, Michael; Strugnell, Jan M; Lieb, Bernhard; Mark, Felix Christopher (2015): DNA alignment and Bayesian trees of partial sequences of COI, COIII and the haemocyanin functional unit f-g of 28 octopod species [dataset]. PANGAEA, https://doi.org/10.1594/PANGAEA.839802, Supplement to: Oellermann, M et al. (2015): Positive selection in octopus haemocyanin indicates functional links to temperature adaptation. BMC Evolutionary Biology, 15, 133-150, https://doi.org/10.1186/s12862-015-0411-4

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Abstract:
Background: Octopods have successfully colonised the world's oceans from the tropics to the poles. Yet, successful persistence in these habitats has required adaptations of their advanced physiological apparatus to compensate impaired oxygen supply. Their oxygen transporter haemocyanin plays a major role in cold tolerance and accordingly has undergone functional modifications to sustain oxygen release at sub-zero temperatures. However, it remains unknown how molecular properties evolved to explain the observed functional adaptations. We thus aimed to assess whether natural selection affected molecular and structural properties of haemocyanin that explains temperature adaptation in octopods.
Results: Analysis of 239 partial sequences of the haemocyanin functional units (FU) f and g of 28 octopod species of polar, temperate, subtropical and tropical origin revealed natural selection was acting primarily on charge properties of surface residues. Polar octopods contained haemocyanins with higher net surface charge due to decreased glutamic acid content and higher numbers of basic amino acids. Within the analysed partial sequences, positive selection was present at site 2545, positioned between the active copper binding centre and the FU g surface. At this site, methionine was the dominant amino acid in polar octopods and leucine was dominant in tropical octopods. Sites directly involved in oxygen binding or quaternary interactions were highly conserved within the analysed sequence.
Conclusions: This study has provided the first insight into molecular and structural mechanisms that have enabled octopods to sustain oxygen supply from polar to tropical conditions. Our findings imply modulation of oxygen binding via charge-charge interaction at the protein surface, which stabilize quaternary interactions among functional units to reduce detrimental effects of high pH on venous oxygen release. Of the observed partial haemocyanin sequence, residue 2545 formed a close link between the FU g surface and the active centre, suggesting a role as allosteric binding site. The prevalence of methionine at this site in polar octopods, implies regulation of oxygen affinity via increased sensitivity to allosteric metal binding. High sequence conservation of sites directly involved in oxygen binding indicates that functional modifications of octopod haemocyanin rather occur via more subtle mechanisms, as observed in this study.
Related to:
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Coverage:
Median Latitude: -19.904138 * Median Longitude: -7.694828 * South-bound Latitude: -70.510000 * West-bound Longitude: -124.430000 * North-bound Latitude: 79.620000 * East-bound Longitude: 169.630000
Parameter(s):
#NameShort NameUnitPrincipal InvestigatorMethod/DeviceComment
1IdentificationIDOellermann, MichaelAnimal identifier
2SpeciesSpeciesOellermann, Michael
3Cruise/expeditionExpeditionOellermann, Michael
4Station labelStationOellermann, Michael
5GearGearOellermann, MichaelFishing gear
6Sampling dateSampling dateOellermann, MichaelDate of capture
7LATITUDELatitudeOellermann, MichaelGeocode
8LONGITUDELongitudeOellermann, MichaelGeocode
9Depth, bathymetricBathy depthmOellermann, Michael
10LocationLocationOellermann, Michael
11Temperature, waterTemp°COellermann, Michaelat depth
12Temperature, water, minimumTemp min°COellermann, Michael
13Temperature, water, maximumTemp max°COellermann, Michael
14Reference/sourceReferenceOellermann, MichaelTemperature
15SalinitySalOellermann, MichaelPSU, at depth
16Salinity, minimumSal minOellermann, Michael
17Salinity, maximumSal maxOellermann, Michael
18Reference/sourceReferenceOellermann, MichaelSalinity
19Sample massSamp mgOellermann, MichaelTotal weight
20Sample massSamp mgOellermann, MichaelGutted weight
21LengthlmmOellermann, MichaelMantle length
22SexSexOellermann, Michael
23CommentCommentOellermann, Michael
Size:
603 data points

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