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Ancient mechanisms for the evolution of the bicoid homeodomain's function in fly development.

Qinwen Liu | Pinar Onal | Rhea R Datta | Julia M Rogers | Urs Schmidt-Ott | Martha L Bulyk | Stephen Small | Joseph W Thornton
eLife | 2018

The ancient mechanisms that caused developmental gene regulatory networks to diversify among distantly related taxa are not well understood. Here we use ancestral protein reconstruction, biochemical experiments, and developmental assays of transgenic animals carrying reconstructed ancestral genes to investigate how the transcription factor Bicoid (Bcd) evolved its central role in anterior-posterior patterning in flies. We show that most of Bcd's derived functions are attributable to evolutionary changes within its homeodomain (HD) during a phylogenetic interval >140 million years ago. A single substitution from this period (Q50K) accounts almost entirely for the evolution of Bcd's derived DNA specificity in vitro. In transgenic embryos expressing the reconstructed ancestral HD, however, Q50K confers activation of only a few of Bcd's transcriptional targets and yields a very partial rescue of anterior development. Adding a second historical substitution (M54R) confers regulation of additional Bcd targets and further rescues anterior development. These results indicate that two epistatically interacting mutations played a major role in the evolution of Bcd's controlling regulatory role in early development. They also show how ancestral sequence reconstruction can be combined with in vivo characterization of transgenic animals to illuminate the historical mechanisms of developmental evolution.

Pubmed ID: 30298815

Research resources used in this publication

None found

Antibodies used in this publication

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Associated grants

  • Agency: NHGRI NIH HHS, United States
    Id: R01 HG005287
  • Agency: NIH HHS, United States
    Id: NSF IOS0744966
  • Agency: NIGMS NIH HHS, United States
    Id: R01 GM121931
  • Agency: NIGMS NIH HHS, United States
    Id: R01 GM051946
  • Agency: NIH HHS, United States
    Id: R01GM051946
  • Agency: NIH HHS, United States
    Id: R01GM104397
  • Agency: NIGMS NIH HHS, United States
    Id: R01 GM104397
  • Agency: NIH HHS, United States
    Id: F32GM112351
  • Agency: NIH HHS, United States
    Id: R01GM121931
  • Agency: NIH HHS, United States
    Id: R01-HG005287
  • Agency: NIH HHS, United States
    Id: IOS1355057

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