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1.
Cell ; 167(3): 633-642.e11, 2016 Oct 20.
Article in English | MEDLINE | ID: mdl-27768887

ABSTRACT

The evolution of body shape is thought to be tightly coupled to changes in regulatory sequences, but specific molecular events associated with major morphological transitions in vertebrates have remained elusive. We identified snake-specific sequence changes within an otherwise highly conserved long-range limb enhancer of Sonic hedgehog (Shh). Transgenic mouse reporter assays revealed that the in vivo activity pattern of the enhancer is conserved across a wide range of vertebrates, including fish, but not in snakes. Genomic substitution of the mouse enhancer with its human or fish ortholog results in normal limb development. In contrast, replacement with snake orthologs caused severe limb reduction. Synthetic restoration of a single transcription factor binding site lost in the snake lineage reinstated full in vivo function to the snake enhancer. Our results demonstrate changes in a regulatory sequence associated with a major body plan transition and highlight the role of enhancers in morphological evolution. PAPERCLIP.


Subject(s)
Biological Evolution , Enhancer Elements, Genetic , Extremities/growth & development , Hedgehog Proteins/genetics , Snakes/genetics , Animals , Base Sequence , Evolution, Molecular , Gene Knock-In Techniques , Mice , Mice, Transgenic , Mutation , Phylogeny , Snakes/classification
2.
Nature ; 554(7691): 239-243, 2018 02 08.
Article in English | MEDLINE | ID: mdl-29420474

ABSTRACT

Distant-acting tissue-specific enhancers, which regulate gene expression, vastly outnumber protein-coding genes in mammalian genomes, but the functional importance of this regulatory complexity remains unclear. Here we show that the pervasive presence of multiple enhancers with similar activities near the same gene confers phenotypic robustness to loss-of-function mutations in individual enhancers. We used genome editing to create 23 mouse deletion lines and inter-crosses, including both single and combinatorial enhancer deletions at seven distinct loci required for limb development. Unexpectedly, none of the ten deletions of individual enhancers caused noticeable changes in limb morphology. By contrast, the removal of pairs of limb enhancers near the same gene resulted in discernible phenotypes, indicating that enhancers function redundantly in establishing normal morphology. In a genetic background sensitized by reduced baseline expression of the target gene, even single enhancer deletions caused limb abnormalities, suggesting that functional redundancy is conferred by additive effects of enhancers on gene expression levels. A genome-wide analysis integrating epigenomic and transcriptomic data from 29 developmental mouse tissues revealed that mammalian genes are very commonly associated with multiple enhancers that have similar spatiotemporal activity. Systematic exploration of three representative developmental structures (limb, brain and heart) uncovered more than one thousand cases in which five or more enhancers with redundant activity patterns were found near the same gene. Together, our data indicate that enhancer redundancy is a remarkably widespread feature of mammalian genomes that provides an effective regulatory buffer to prevent deleterious phenotypic consequences upon the loss of individual enhancers.


Subject(s)
Enhancer Elements, Genetic/genetics , Extremities/embryology , Gene Expression Regulation, Developmental/genetics , Phenotype , Animals , Brain/embryology , Female , Genome , Heart/embryology , Limb Deformities, Congenital/embryology , Limb Deformities, Congenital/genetics , Male , Mice , Sequence Deletion , Spatio-Temporal Analysis
3.
Cell Rep ; 31(1): 107490, 2020 04 07.
Article in English | MEDLINE | ID: mdl-32268095

ABSTRACT

Digit loss/reductions are evolutionary adaptations in cursorial mammals such as pigs. To gain mechanistic insight into these processes, we performed a comparative molecular analysis of limb development in mouse and pig embryos, which revealed a loss of anterior-posterior polarity during distal progression of pig limb bud development. These alterations in pig limb buds are paralleled by changes in the mesenchymal response to Sonic hedgehog (SHH) signaling, which is altered upstream of the reduction and loss of Fgf8 expression in the ectoderm that overlaps the reduced and vestigial digit rudiments of the pig handplate, respectively. Furthermore, genome-wide open chromatin profiling using equivalent developmental stages of mouse and pig limb buds reveals the functional divergence of about one-third of the regulatory genome. This study uncovers widespread alterations in the regulatory landscapes of genes essential for limb development that likely contributed to the morphological diversion of artiodactyl limbs from the pentadactyl archetype of tetrapods.


Subject(s)
Body Patterning/genetics , Limb Buds/embryology , Limb Buds/metabolism , Animals , Biological Evolution , Ectoderm/metabolism , Extremities/embryology , Female , Gene Expression Regulation, Developmental/genetics , Male , Mesoderm/metabolism , Mice/embryology , Phenotype , Polydactyly/genetics , Signal Transduction/genetics , Swine/embryology , Trans-Activators/metabolism
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