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DOI | 10.1073/pnas.2100694118 |
Longer or shorter spines: Reciprocal trait evolution in stickleback via triallelic regulatory changes in Stanniocalcin2a | |
Roberts Kingman G.A.; Lee D.; Jones F.C.; Desmet D.; Bell M.A.; Kingsley D.M. | |
发表日期 | 2021 |
ISSN | 0027-8424 |
卷号 | 118期号:31 |
英文摘要 | Vertebrates have repeatedly modified skeletal structures to adapt to their environments. The threespine stickleback is an excellent system for studying skeletal modifications, as different wild populations have either increased or decreased the lengths of their prominent dorsal and pelvic spines in different freshwater environments. Here we identify a regulatory locus that has a major morphological effect on the length of stickleback dorsal and pelvic spines, which we term Maser (major spine enhancer). Maser maps in a closely linked supergene complex that controls multiple armor, feeding, and behavioral traits on chromosome IV. Natural alleles in Maser are differentiated between marine and freshwater sticklebacks; however, alleles found among freshwater populations are also differentiated, with distinct alleles found in short- and long-spined freshwater populations. The distinct freshwater alleles either increase or decrease expression of the bone growth inhibitor gene Stanniocalcin2a in developing spines, providing a simple genetic mechanism for either increasing or decreasing spine lengths in natural populations. Genomic surveys suggest many recurrently differentiated loci in sticklebacks are similarly specialized into three or more distinct alleles, providing multiple ancient standing variants in particular genes that may contribute to a range of phenotypes in different environments. © 2021 National Academy of Sciences. All rights reserved. |
英文关键词 | Multiallelic polymorphism; Regulatory evolution; Stanniocalcin; Stickleback spine length; Supergene |
语种 | 英语 |
scopus关键词 | fish protein; signal peptide; allele; animal; animal structures; evolution; female; gene expression regulation; genetics; genomics; genotype; growth, development and aging; male; metabolism; physiology; polymerase chain reaction; quantitative trait locus; Smegmamorpha; Alleles; Animal Structures; Animals; Biological Evolution; Female; Fish Proteins; Gene Expression Regulation, Developmental; Genomics; Genotype; Intercellular Signaling Peptides and Proteins; Male; Polymerase Chain Reaction; Quantitative Trait Loci; Smegmamorpha |
来源期刊 | Proceedings of the National Academy of Sciences of the United States of America
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文献类型 | 期刊论文 |
条目标识符 | http://gcip.llas.ac.cn/handle/2XKMVOVA/251088 |
作者单位 | Department of Developmental Biology, Stanford University, School of Medicine, Stanford, CA 94305, United States; Stanford University, School of Humanities and Sciences, Stanford University, Stanford, CA 94305, United States; University of California Museum of Paleontology, University of California, Berkeley, CA 94720, United States; HHMI, Stanford University, School of Medicine, Stanford, CA 94305, United States; Friedrich Miescher Laboratory of the Max Planck Society, Tübingen, 72076, Germany; Division of Research and Development, Upside Foods, Berkeley, CA 94710, United States |
推荐引用方式 GB/T 7714 | Roberts Kingman G.A.,Lee D.,Jones F.C.,et al. Longer or shorter spines: Reciprocal trait evolution in stickleback via triallelic regulatory changes in Stanniocalcin2a[J],2021,118(31). |
APA | Roberts Kingman G.A.,Lee D.,Jones F.C.,Desmet D.,Bell M.A.,&Kingsley D.M..(2021).Longer or shorter spines: Reciprocal trait evolution in stickleback via triallelic regulatory changes in Stanniocalcin2a.Proceedings of the National Academy of Sciences of the United States of America,118(31). |
MLA | Roberts Kingman G.A.,et al."Longer or shorter spines: Reciprocal trait evolution in stickleback via triallelic regulatory changes in Stanniocalcin2a".Proceedings of the National Academy of Sciences of the United States of America 118.31(2021). |
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