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  Evaluating the maintenance of disease-associated variation at the blood group-related gene B4galnt2 in house mice

Vallier, M., Abou Chakra, M., Hindersin, L., Linnenbrink, M., Traulsen, A., & Baines, J. F. (2017). Evaluating the maintenance of disease-associated variation at the blood group-related gene B4galnt2 in house mice. BMC Evolutionary Biology, 17(187), 1-22. doi:10.1186/s12862-017-1035-7.

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 Urheber:
Vallier, Marie1, Autor           
Abou Chakra, Maria2, Autor           
Hindersin, Laura2, Autor           
Linnenbrink, Miriam3, Autor           
Traulsen, Arne2, Autor           
Baines, John F.1, Autor           
Affiliations:
1Guest Group Evolutionary Genomics, Max Planck Institute for Evolutionary Biology, Max Planck Society, ou_1445638              
2Department Evolutionary Theory, Max Planck Institute for Evolutionary Biology, Max Planck Society, ou_1445641              
3Department Evolutionary Genetics, Max Planck Institute for Evolutionary Biology, Max Planck Society, ou_1445635              

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Schlagwörter: B4galnt2; Blood group; Host-pathogen interaction; Balancing selection; Trade-off; Evolutionary game theory; Wright-fisher process
 Zusammenfassung: B4galnt2 is a blood group-related glycosyltransferase that displays cis-regulatory variation for its tissue-specific expression patterns in house mice. The wild type allele, found e.g. in the C57BL/6 J strain, directs intestinal expression of B4galnt2, which is the pattern observed among vertebrates, including humans. An alternative allele class found in the RIIIS/J strain and other mice instead drives expression in blood vessels, which leads to a phenotype similar to type 1 von Willebrand disease (VWD), a common human bleeding disorder. We previously showed that alternative B4galnt2 alleles are subject to long-term balancing selection in mice and that variation in B4galnt2 expression influences host-microbe interactions in the intestine. This suggests that the costs of prolonged bleeding in RIIIS/J allele-bearing mice might be outweighed by benefits associated with resistance against gastrointestinal pathogens. However, the conditions under which such trade-offs could lead to the long-term maintenance of disease-associated variation at B4galnt2 are unclear.

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Sprache(n): eng - English
 Datum: 2017-03-272017-08-042017-08-14
 Publikationsstatus: Online veröffentlicht
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 Identifikatoren: DOI: 10.1186/s12862-017-1035-7
BibTex Citekey: Vallier2017
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Titel: BMC Evolutionary Biology
Genre der Quelle: Zeitschrift
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Ort, Verlag, Ausgabe: BioMed Central
Seiten: 22 Band / Heft: 17 (187) Artikelnummer: - Start- / Endseite: 1 - 22 Identifikator: ISSN: 1471-2148
CoNE: https://pure.mpg.de/cone/journals/resource/111000136905006