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Evolution of the functionally conserved DCC gene in birds
Umeå universitet, Medicinska fakulteten, Umeå centrum för molekylär medicin (UCMM).
Umeå universitet, Medicinska fakulteten, Umeå centrum för molekylär medicin (UCMM).
Umeå universitet, Medicinska fakulteten, Umeå centrum för molekylär medicin (UCMM).
Umeå universitet, Medicinska fakulteten, Umeå centrum för molekylär medicin (UCMM).
2017 (engelsk)Inngår i: Scientific Reports, E-ISSN 2045-2322, Vol. 7, artikkel-id 42029Artikkel i tidsskrift (Fagfellevurdert) Published
Abstract [en]

Understanding the loss of conserved genes is critical for determining how phenotypic diversity is generated. Here we focus on the evolution of DCC, a gene that encodes a highly conserved neural guidance receptor. Disruption of DCC in animal models and humans results in major neurodevelopmental defects including commissural axon defects. Here we examine DCC evolution in birds, which is of particular interest as a major model system in neurodevelopmental research. We found the DCC containing locus was disrupted several times during evolution, resulting in both gene losses and faster evolution rate of salvaged genes. These data suggest that DCC had been lost independently twice during bird evolution, including in chicken and zebra finch, whereas it was preserved in many other closely related bird species, including ducks. Strikingly, we observed that commissural axon trajectory appeared similar regardless of whether DCC could be detected or not. We conclude that the DCC locus is susceptible to genomic instability leading to independent disruptions in different branches of birds and a significant influence on evolution rate. Overall, the phenomenon of loss or molecular evolution of a highly conserved gene without apparent phenotype change is of conceptual importance for understanding molecular evolution of key biological processes.

sted, utgiver, år, opplag, sider
Macmillan Publishers Ltd., 2017. Vol. 7, artikkel-id 42029
Emneord [en]
embryology, evolutionary developmental biology, neuronal development
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Identifikatorer
URN: urn:nbn:se:umu:diva-131968DOI: 10.1038/srep42029ISI: 000394782700001Scopus ID: 2-s2.0-85014088301OAI: oai:DiVA.org:umu-131968DiVA, id: diva2:1077400
Tilgjengelig fra: 2017-02-27 Laget: 2017-02-27 Sist oppdatert: 2023-03-23bibliografisk kontrollert

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Patthey, CedricTong, Yong GuangTait, Christine MaryWilson, Sara Ivy

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