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   <subfield code="a">10.1007/s00239-011-9469-9</subfield>
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   <subfield code="a">Evolution of the TOR Pathway</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Teunis van Dam, Fried Zwartkruis, Johannes Bos, Berend Snel]</subfield>
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   <subfield code="a">The TOR kinase is a major regulator of growth in eukaryotes. Many components of the TOR pathway are implicated in cancer and metabolic diseases in humans. Analysis of the evolution of TOR and its pathway may provide fundamental insight into the evolution of growth regulation in eukaryotes and provide a practical framework on which experimental evidence can be compared between species. Here we performed phylogenetic analyses on the components of the TOR pathway and determined their point of invention. We find that the two TOR complexes and a large part of the TOR pathway originated before the Last Eukaryotic Common Ancestor and form a core to which new inputs have been added during animal evolution. In addition, we provide insight into how duplications and sub-functionalization of the S6K, RSK, SGK and PKB kinases shaped the complexity of the TOR pathway. In yeast we identify novel AGC kinases that are orthologous to the S6 kinase. These results demonstrate how a vital signaling pathway can be both highly conserved and flexible in eukaryotes.</subfield>
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   <subfield code="a">The Author(s), 2011</subfield>
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   <subfield code="a">TOR</subfield>
   <subfield code="2">nationallicence</subfield>
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   <subfield code="a">Pathway evolution</subfield>
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   <subfield code="a">Rheb</subfield>
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   <subfield code="u">Department Molecular Cancer Research, University Medical Center Utrecht, Universiteitsweg 100, 3584 CG, Utrecht, The Netherlands</subfield>
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   <subfield code="g">73/3-4(2011-10-01), 209-220</subfield>
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   <subfield code="b">Springer special CC-BY-NC licence</subfield>
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