Reptilian heart development and the molecular basis of cardiac chamber evolution
Heart to heart Birds, mammals and crocodiles have hearts with two separate ventricles, servicing separate pulmonary and systemic circulations. Amphibians have just one ventricle, but in most reptiles, the situation is unclear. A new embryological study of a lizard (the green anole) and a turtle (the...
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Published in | Nature (London) Vol. 461; no. 7260; pp. 95 - 98 |
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Main Authors | , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
London
Nature Publishing Group UK
03.09.2009
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
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Summary: | Heart to heart
Birds, mammals and crocodiles have hearts with two separate ventricles, servicing separate pulmonary and systemic circulations. Amphibians have just one ventricle, but in most reptiles, the situation is unclear. A new embryological study of a lizard (the green anole) and a turtle (the slider turtle) shows that the division of an ancestral single ventricle into two chambers is related to the expression of the T-box transcription factor
Tbx5
. In embryonic birds and mammals, Tbx5 expression is restricted to precursors of the left ventricle. In turtles and lizards,
Tbx5
is initially expressed throughout the ventricle, but in turtles (though not lizards) it is later restricted to the left side of the chamber. This identifies altered
Tbx5
expression as a possible evolutionary force driving embryonic heart patterning to provide the key adaptation to high-energy terrestrial life, the fully septated heart. In line with this idea, mice in which
Tbx5
function is lost or expanded develop a single chamber lacking distinct identity.
The hearts of birds, mammals and crocodiles have two ventricles serving separate pulmonary and systemic circulations, whereas the hearts of amphibians have only one ventricle. In most reptiles, however, the situation is unclear, which is of interest in the context of the evolution of cardiac septation. Here, gene expression in the developing ventricles of two reptiles is analysed; the results suggest a role for the T-box transcription factor
Tbx5
.
The emergence of terrestrial life witnessed the need for more sophisticated circulatory systems. This has evolved in birds, mammals and crocodilians into complete septation of the heart into left and right sides, allowing separate pulmonary and systemic circulatory systems, a key requirement for the evolution of endothermy
1
,
2
,
3
. However, the evolution of the amniote heart is poorly understood. Reptilian hearts have been the subject of debate in the context of the evolution of cardiac septation: do they possess a single ventricular chamber or two incompletely septated ventricles
4
,
5
,
6
,
7
? Here we examine heart development in the red-eared slider turtle,
Trachemys scripta elegans
(a chelonian), and the green anole,
Anolis carolinensis
(a squamate), focusing on gene expression in the developing ventricles. Both reptiles initially form a ventricular chamber that homogenously expresses the T-box transcription factor gene
Tbx5
. In contrast, in birds and mammals,
Tbx5
is restricted to left ventricle precursors
8
,
9
. In later stages,
Tbx5
expression in the turtle (but not anole) heart is gradually restricted to a distinct left ventricle, forming a left–right gradient. This suggests that
Tbx5
expression was refined during evolution to pattern the ventricles. In support of this hypothesis, we show that loss of
Tbx5
in the mouse ventricle results in a single chamber lacking distinct identity, indicating a requirement for
Tbx5
in septation. Importantly, misexpression of
Tbx5
throughout the developing myocardium to mimic the reptilian expression pattern also results in a single mispatterned ventricular chamber lacking septation. Thus ventricular septation is established by a steep and correctly positioned
Tbx5
gradient. Our findings provide a molecular mechanism for the evolution of the amniote ventricle, and support the concept that altered expression of developmental regulators is a key mechanism of vertebrate evolution. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 These authors contributed equally to this work Author Contributions. K.K-T. performed reptile histology and gene expression studies; A.D.M., B.K., T.S., and B.G.B. performed mouse experiments; J.C.-T. and S.F.G. obtained turtle specimens and isolated T. scripta Tbx5 cDNA; S.L. and L.B. isolated Anolis specimens under direction of J.W.; B.K. acquired and reconstructed OPT images; R.O.G. performed Tbx5 immunohistochemistry under direction of M.N.; R.M.H. directed initial mouse embryo OPT; J.K.T. obtained chick and mouse specimens; R.O.G., M.N., B.L.B., and E.N.O. provided genetically modified mice prior to publication; B.G.B. conceived and directed the project, and wrote the paper. All authors contributed to the written manuscript. |
ISSN: | 0028-0836 1476-4687 1476-4687 |
DOI: | 10.1038/nature08324 |