Abstract
Transcriptional enhancers orchestrate cell type- and time point-specific gene expression programs. Genetic variation within enhancer sequences is an important contributor to phenotypic variation including evolutionary adaptations and human disease. Certain genes and pathways may be more prone to regulatory evolution than others, with different patterns across diverse organisms, but whether such patterns exist has not been investigated at a sufficient scale. To address this question, we identified signatures of accelerated sequence evolution in conserved enhancer elements throughout the mammalian phylogeny at an unprecedented scale. While different genes and pathways were enriched for regulatory evolution in different parts of the tree, we found a striking overall pattern of pleiotropic genes involved in gene regulatory and developmental processes being enriched for accelerated enhancer evolution. These genes were connected to more enhancers than other genes, which was the basis for having an increased amount of sequence acceleration over all their enhancers combined. We provide evidence that sequence acceleration is associated with turnover of regulatory function. Detailed study of one acceleration event in an enhancer of HES1 revealed that sequence evolution led to a new activity domain in the developing limb that emerged concurrently with the evolution of digit reduction in hoofed mammals. Our results provide evidence that enhancer evolution has been a frequent contributor to regulatory innovation at conserved developmental signaling genes in mammals.
Original language | English |
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Article number | msae199 |
Journal | Molecular Biology and Evolution |
Volume | 41 |
Issue number | 10 |
Early online date | 20 Sept 2024 |
DOIs | |
Publication status | Published - Oct 2024 |
Bibliographical note
Publisher Copyright:© The Author(s) 2024. Published by Oxford University Press on behalf of Society for Molecular Biology and Evolution.
Funding
This work was supported by National Institutes of Health awards R01 HD102030 (to J.P.N.) and F32 HD108935 (to M.B.). This research program and related results were also made possible by the support of the NOMIS foundation (to J.P.N.).
Funders | Funder number |
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National Institutes of Health | R01 HD102030, F32 HD108935 |
NOMIS foundation |
Keywords
- Conserved non-coding sequences
- enhancer evolution
- mammal evolution
- notch signaling
- sequence acceleration