A refined model of the genomic basis for phenotypic variation in vertebrate hemostasis

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A refined model of the genomic basis for phenotypic variation in vertebrate hemostasis. / Ribeiro, Ângela M.; Zepeda Mendoza, Marie Lisandra; Bertelsen, Mads Frost; Kristensen, Annemarie Thuri; Jarvis, Erich D.; Gilbert, M Thomas P; Rodrigues da Fonseca, Rute Andreia.

In: B M C Evolutionary Biology, Vol. 15, 124, 2015.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Ribeiro, ÂM, Zepeda Mendoza, ML, Bertelsen, MF, Kristensen, AT, Jarvis, ED, Gilbert, MTP & Rodrigues da Fonseca, RA 2015, 'A refined model of the genomic basis for phenotypic variation in vertebrate hemostasis', B M C Evolutionary Biology, vol. 15, 124. https://doi.org/10.1186/s12862-015-0409-y

APA

Ribeiro, Â. M., Zepeda Mendoza, M. L., Bertelsen, M. F., Kristensen, A. T., Jarvis, E. D., Gilbert, M. T. P., & Rodrigues da Fonseca, R. A. (2015). A refined model of the genomic basis for phenotypic variation in vertebrate hemostasis. B M C Evolutionary Biology, 15, [124]. https://doi.org/10.1186/s12862-015-0409-y

Vancouver

Ribeiro ÂM, Zepeda Mendoza ML, Bertelsen MF, Kristensen AT, Jarvis ED, Gilbert MTP et al. A refined model of the genomic basis for phenotypic variation in vertebrate hemostasis. B M C Evolutionary Biology. 2015;15. 124. https://doi.org/10.1186/s12862-015-0409-y

Author

Ribeiro, Ângela M. ; Zepeda Mendoza, Marie Lisandra ; Bertelsen, Mads Frost ; Kristensen, Annemarie Thuri ; Jarvis, Erich D. ; Gilbert, M Thomas P ; Rodrigues da Fonseca, Rute Andreia. / A refined model of the genomic basis for phenotypic variation in vertebrate hemostasis. In: B M C Evolutionary Biology. 2015 ; Vol. 15.

Bibtex

@article{6d7d8b6816e841c09770d2de7a19ed47,
title = "A refined model of the genomic basis for phenotypic variation in vertebrate hemostasis",
abstract = "BACKGROUND: Hemostasis is a defense mechanism that enhances an organism's survival by minimizing blood loss upon vascular injury. In vertebrates, hemostasis has been evolving with the cardio-vascular and hemodynamic systems over the last 450 million years. Birds and mammals have very similar vascular and hemodynamic systems, thus the mechanism that blocks ruptures in the vasculature is expected to be the same. However, the speed of the process varies across vertebrates, and is particularly slow for birds. Understanding the differences in the hemostasis pathway between birds and mammals, and placing them in perspective to other vertebrates may provide clues to the genetic contribution to variation in blood clotting phenotype in vertebrates. We compiled genomic data corresponding to key elements involved in hemostasis across vertebrates to investigate its genetic basis and understand how it affects fitness.RESULTS: We found that: i) fewer genes are involved in hemostasis in birds compared to mammals; and ii) the largest differences concern platelet membrane receptors and components from the kallikrein-kinin system. We propose that lack of the cytoplasmic domain of the GPIb receptor subunit alpha could be a strong contributor to the prolonged bleeding phenotype in birds. Combined analysis of laboratory assessments of avian hemostasis with the first avian phylogeny based on genomic-scale data revealed that differences in hemostasis within birds are not explained by phylogenetic relationships, but more so by genetic variation underlying components of the hemostatic process, suggestive of natural selection.CONCLUSIONS: This work adds to our understanding of the evolution of hemostasis in vertebrates. The overlap with the inflammation, complement and renin-angiotensin (blood pressure regulation) pathways is a potential driver of rapid molecular evolution in the hemostasis network. Comparisons between avian species and mammals allowed us to hypothesize that the observed mammalian innovations might have contributed to the diversification of mammals that give birth to live young.",
author = "Ribeiro, {{\^A}ngela M.} and {Zepeda Mendoza}, {Marie Lisandra} and Bertelsen, {Mads Frost} and Kristensen, {Annemarie Thuri} and Jarvis, {Erich D.} and Gilbert, {M Thomas P} and {Rodrigues da Fonseca}, {Rute Andreia}",
year = "2015",
doi = "10.1186/s12862-015-0409-y",
language = "English",
volume = "15",
journal = "B M C Evolutionary Biology",
issn = "1471-2148",
publisher = "BioMed Central Ltd.",

}

RIS

TY - JOUR

T1 - A refined model of the genomic basis for phenotypic variation in vertebrate hemostasis

AU - Ribeiro, Ângela M.

AU - Zepeda Mendoza, Marie Lisandra

AU - Bertelsen, Mads Frost

AU - Kristensen, Annemarie Thuri

AU - Jarvis, Erich D.

AU - Gilbert, M Thomas P

AU - Rodrigues da Fonseca, Rute Andreia

PY - 2015

Y1 - 2015

N2 - BACKGROUND: Hemostasis is a defense mechanism that enhances an organism's survival by minimizing blood loss upon vascular injury. In vertebrates, hemostasis has been evolving with the cardio-vascular and hemodynamic systems over the last 450 million years. Birds and mammals have very similar vascular and hemodynamic systems, thus the mechanism that blocks ruptures in the vasculature is expected to be the same. However, the speed of the process varies across vertebrates, and is particularly slow for birds. Understanding the differences in the hemostasis pathway between birds and mammals, and placing them in perspective to other vertebrates may provide clues to the genetic contribution to variation in blood clotting phenotype in vertebrates. We compiled genomic data corresponding to key elements involved in hemostasis across vertebrates to investigate its genetic basis and understand how it affects fitness.RESULTS: We found that: i) fewer genes are involved in hemostasis in birds compared to mammals; and ii) the largest differences concern platelet membrane receptors and components from the kallikrein-kinin system. We propose that lack of the cytoplasmic domain of the GPIb receptor subunit alpha could be a strong contributor to the prolonged bleeding phenotype in birds. Combined analysis of laboratory assessments of avian hemostasis with the first avian phylogeny based on genomic-scale data revealed that differences in hemostasis within birds are not explained by phylogenetic relationships, but more so by genetic variation underlying components of the hemostatic process, suggestive of natural selection.CONCLUSIONS: This work adds to our understanding of the evolution of hemostasis in vertebrates. The overlap with the inflammation, complement and renin-angiotensin (blood pressure regulation) pathways is a potential driver of rapid molecular evolution in the hemostasis network. Comparisons between avian species and mammals allowed us to hypothesize that the observed mammalian innovations might have contributed to the diversification of mammals that give birth to live young.

AB - BACKGROUND: Hemostasis is a defense mechanism that enhances an organism's survival by minimizing blood loss upon vascular injury. In vertebrates, hemostasis has been evolving with the cardio-vascular and hemodynamic systems over the last 450 million years. Birds and mammals have very similar vascular and hemodynamic systems, thus the mechanism that blocks ruptures in the vasculature is expected to be the same. However, the speed of the process varies across vertebrates, and is particularly slow for birds. Understanding the differences in the hemostasis pathway between birds and mammals, and placing them in perspective to other vertebrates may provide clues to the genetic contribution to variation in blood clotting phenotype in vertebrates. We compiled genomic data corresponding to key elements involved in hemostasis across vertebrates to investigate its genetic basis and understand how it affects fitness.RESULTS: We found that: i) fewer genes are involved in hemostasis in birds compared to mammals; and ii) the largest differences concern platelet membrane receptors and components from the kallikrein-kinin system. We propose that lack of the cytoplasmic domain of the GPIb receptor subunit alpha could be a strong contributor to the prolonged bleeding phenotype in birds. Combined analysis of laboratory assessments of avian hemostasis with the first avian phylogeny based on genomic-scale data revealed that differences in hemostasis within birds are not explained by phylogenetic relationships, but more so by genetic variation underlying components of the hemostatic process, suggestive of natural selection.CONCLUSIONS: This work adds to our understanding of the evolution of hemostasis in vertebrates. The overlap with the inflammation, complement and renin-angiotensin (blood pressure regulation) pathways is a potential driver of rapid molecular evolution in the hemostasis network. Comparisons between avian species and mammals allowed us to hypothesize that the observed mammalian innovations might have contributed to the diversification of mammals that give birth to live young.

U2 - 10.1186/s12862-015-0409-y

DO - 10.1186/s12862-015-0409-y

M3 - Journal article

C2 - 26123414

VL - 15

JO - B M C Evolutionary Biology

JF - B M C Evolutionary Biology

SN - 1471-2148

M1 - 124

ER -

ID: 146255395