ABSTRACT
Epigenetic mechanisms may play a central role in mediating phenotypic plasticity, especially during range expansions, when populations face a suite of novel environmental conditions. Individuals may differ in their epigenetic potential (EP; their capacity for epigenetic modifications of gene expression), which may affect their ability to colonize new areas. One form of EP, the number of CpG sites, is higher in introduced house sparrows (Passer domesticus) than in native birds in the promoter region of a microbial surveillance gene, Toll-like Receptor 4 (TLR4), which may allow invading birds to fine-tune their immune responses to unfamiliar parasites. Here, we compared TLR4 gene expression from whole blood, liver and spleen in house sparrows with different EP, first challenging some birds with lipopolysaccharide (LPS), to increase gene expression by simulating a natural infection. We expected that high EP would predict high inducibility and reversibility of TLR4 expression in the blood of birds treated with LPS, but we did not make directional predictions regarding organs, as we could not repeatedly sample these tissues. We found that EP was predictive of TLR4 expression in all tissues. Birds with high EP expressed more TLR4 in the blood than individuals with low EP, regardless of treatment with LPS. Only females with high EP exhibited reversibility in gene expression. Further, the effect of EP varied between sexes and among tissues. Together, these data support EP as one regulator of TLR4 expression.
Footnotes
Competing interests
The authors declare no competing or financial interests.
Author contributions
Conceptualization: H.E.H., C.Z., A.W.S., L.B.M.; Formal analysis: H.E.H., C.Z.; Investigation: H.E.H., C.Z., B.K., A.W.S., J.D.M.; Writing - original draft: H.E.H.; Writing- reviewing and editing: H.E.H., C.Z., B.K., A.W.S, J.D.M, L.B.M.; Project administration: L.B.M.
Funding
This work was supported by the National Science Foundation (grant number 2027040), the University of South Florida College of Public Health, and the Pritzker Laboratory for Molecular Systematics and Evolution. H.E.H. thanks Sigma XI (G2016100191872782), the Porter Family Foundation, the American Ornithological Society Hesse Grant, the American Museum of Natural History Frank M. Chapman Memorial Fund, and the National Science Foundation Research Coordination Network g2p2pop Laboratory Exchange Grant for support.
Data availability
DNA sequences can be accessed via GenBank accession numbers MW557619 MW557649. Supporting data can be accessed at https://doi.org/10.6084/m9.figshare.13670119.v1.
Supplementary information
Supplementary information available online at https://jeb.biologists.org/lookup/doi/10.1242/jeb.238451.supplemental
- Received October 6, 2020.
- Accepted February 6, 2021.
- © 2021. Published by The Company of Biologists Ltd
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