Author
Listed:
- Juliana G. Roscito
(Max Planck Institute of Molecular Cell Biology and Genetics
Max Planck Institute for the Physics of Complex Systems
Center for Systems Biology Dresden
Universidade de São Paulo)
- Katrin Sameith
(Max Planck Institute of Molecular Cell Biology and Genetics
Max Planck Institute for the Physics of Complex Systems
Center for Systems Biology Dresden)
- Genis Parra
(Max Planck Institute of Molecular Cell Biology and Genetics
Max Planck Institute for the Physics of Complex Systems
Center for Systems Biology Dresden)
- Bjoern E. Langer
(Max Planck Institute of Molecular Cell Biology and Genetics
Max Planck Institute for the Physics of Complex Systems
Center for Systems Biology Dresden)
- Andreas Petzold
(Center for Regenerative Therapies TU Dresden)
- Claudia Moebius
(Max Planck Institute of Molecular Cell Biology and Genetics)
- Marc Bickle
(Max Planck Institute of Molecular Cell Biology and Genetics)
- Miguel Trefaut Rodrigues
(Universidade de São Paulo)
- Michael Hiller
(Max Planck Institute of Molecular Cell Biology and Genetics
Max Planck Institute for the Physics of Complex Systems
Center for Systems Biology Dresden)
Abstract
Detecting the genomic changes underlying phenotypic changes between species is a main goal of evolutionary biology and genomics. Evolutionary theory predicts that changes in cis-regulatory elements are important for morphological changes. We combined genome sequencing, functional genomics and genome-wide comparative analyses to investigate regulatory elements in lineages that lost morphological traits. We first show that limb loss in snakes is associated with widespread divergence of limb regulatory elements. We next show that eye degeneration in subterranean mammals is associated with widespread divergence of eye regulatory elements. In both cases, sequence divergence results in an extensive loss of transcription factor binding sites. Importantly, diverged regulatory elements are associated with genes required for normal limb patterning or normal eye development and function, suggesting that regulatory divergence contributed to the loss of these phenotypes. Together, our results show that genome-wide decay of the phenotype-specific cis-regulatory landscape is a hallmark of lost morphological traits.
Suggested Citation
Juliana G. Roscito & Katrin Sameith & Genis Parra & Bjoern E. Langer & Andreas Petzold & Claudia Moebius & Marc Bickle & Miguel Trefaut Rodrigues & Michael Hiller, 2018.
"Phenotype loss is associated with widespread divergence of the gene regulatory landscape in evolution,"
Nature Communications, Nature, vol. 9(1), pages 1-15, December.
Handle:
RePEc:nat:natcom:v:9:y:2018:i:1:d:10.1038_s41467-018-07122-z
DOI: 10.1038/s41467-018-07122-z
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Cited by:
- Rong Hua & Yuan-Shuo Ma & Lu Yang & Jun-Jun Hao & Qin-Yang Hua & Lu-Ye Shi & Xiao-Qing Yao & Hao-Yu Zhi & Zhen Liu, 2024.
"Experimental evidence for cancer resistance in a bat species,"
Nature Communications, Nature, vol. 15(1), pages 1-15, December.
- Mario Ivanković & Jeremias N. Brand & Luca Pandolfini & Thomas Brown & Martin Pippel & Andrei Rozanski & Til Schubert & Markus A. Grohme & Sylke Winkler & Laura Robledillo & Meng Zhang & Azzurra Codin, 2024.
"A comparative analysis of planarian genomes reveals regulatory conservation in the face of rapid structural divergence,"
Nature Communications, Nature, vol. 15(1), pages 1-21, December.
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