ArticleFrontiers in zoology2014
New developmental evidence supports a homeotic frameshift of digit identity in the evolution of the bird wing.
Article in Frontiers in zoology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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10 citing papers in PubMed, 22 citations in OpenAlex.
- Insights into digit evolution from a fate map study of the forearm using Chameleon, a new transgenic chicken line.Development (Cambridge, England) · 2024Article
- Selection on Phalanx Development in the Evolution of the Bird Wing.Molecular biology and evolution · 2021Article
- Evidence against tetrapod-wide digit identities and for a limited frame shift in bird wings.Nature communications · 2019Article
- Morphogenetic mechanism of the acquisition of the dinosaur-type acetabulum.Royal Society open science · 2018Article
- Evolution of antero-posterior patterning of the limb: Insights from the chick.Genesis (New York, N.Y. : 2000) · 2018Review
- The origins, scaling and loss of tetrapod digits.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2017Review
- Deep homology in the age of next-generation sequencing.Philosophical transactions of the Royal Society of London. Series B, Biological sciences · 2017Review
- What limits the morphological disparity of clades?Interface focus · 2015Article
- The phantoms of a high-seven - or - why do our thumbs stick out?Frontiers in zoology · 2015Article
- New developmental evidence clarifies the evolution of wrist bones in the dinosaur-bird transition.PLoS biology · 2014Article
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Authors and funding
6 authors at 1 institution in 1 country.
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No grant is acknowledged in the PubMed record.
Abstract
backgroundThe homology of the digits in the bird wing is a high-profile controversy in developmental and evolutionary biology. The embryonic position of the digits cartilages with respect to the primary axis (ulnare and ulna) corresponds to 2, 3, 4, but comparative-evolutionary morphology supports 1, 2, 3. A homeotic frameshift of digit identity in evolution could explain how cells in embryonic positions 2, 3, 4 began developing morphologies 1, 2, 3. Another alternative is that no re-patterning of cell fates occurred, and the primary axis shifted its position by some other mechanism. In the wing, only the anterior digit lacks expression of HoxD10 and HoxD12, resembling digit 1 of other limbs, as predicted by 1, 2, 3. However, upon loss of digit 1 in evolution, the most anterior digit 2 could have lost their expression, deceitfully resembling a digit 1. To test this notion, we observed HoxD10 and HoxD12 in a limb where digit 2 is the most anterior digit: The rabbit foot. We also explored whether early inhibition of Shh signalling in the embryonic wing bud induces an experimental homeotic frameshift, or an experimental axis shift. We tested these hypotheses using DiI injections to study the fate of cells in these experimental wings.
resultsWe found strong transcription of HoxD10 and HoxD12 was present in the most anterior digit 2 of the rabbit foot. Thus, we found no evidence to question the use of HoxD expression as support for 1, 2, 3. When Shh signalling in early wing buds is inhibited, our fate maps demonstrate that an experimental homeotic frameshift is induced.
conclusionAlong with comparative morphology, HoxD expression provides strong support for 1, 2, 3 identity of wing digits. As an explanation for the offset 2, 3, 4 embryological position, the homeotic frameshift hypothesis is consistent with known mechanisms of limb development, and further proven to be experimentally possible. In contrast, the underlying mechanisms and experimental plausibility of an axis shift remain unclear.
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