4.8 Article

Coevolution between MHC Class I and Antigen-Processing Genes in Salamanders

期刊

MOLECULAR BIOLOGY AND EVOLUTION
卷 38, 期 11, 页码 5092-5106

出版社

OXFORD UNIV PRESS
DOI: 10.1093/molbev/msab237

关键词

major histocompatibility complex; antigen-processing genes; coevolution; Urodela; comparative methods

资金

  1. Polish National Science Centre [2016/23/B/NZ8/00738]
  2. PROTEUS project in Croatia
  3. University of Connecticut Research Foundation
  4. KAKENHI from the Japan Society for the Promotion of Science [JP16K18613]
  5. Foundation for Polish Science (FNP) START stipend
  6. Polish National Science Centre Sonatina 3 [2019/32/C/NZ8/00440]
  7. National Research, Development and Innovation Fund of Hungary [KH130360]
  8. National Research Foundation of Korea (Ministry of Education) [2015R1D1A01057282]
  9. Ministry of Science, ICT, and Future Planning [2018R1A2B6006833]
  10. BioS Priority Research Area under the program Excellence Initiative Research University at the Jagiellonian University in Krakow, Poland
  11. National Research Foundation of Korea [2018R1A2B6006833] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)

向作者/读者索取更多资源

The study found a positive correlation between MHC-I diversity and the diversity of two APGs (TAP1 and TAP2) in salamanders, supporting their coevolution. However, no consistent effect was detected for the other three APGs (PSMB8, PSMB9, and TAPBP). This suggests that while coevolution occurs in salamanders, it does not limit the expansion of the MHC-I gene family.
Proteins encoded by antigen-processing genes (APGs) provide major histocompatibility complex (MHC) class I (MHC-I) with antigenic peptides. In mammals, polymorphic multigenic MHC-I family is served by monomorphic APGs, whereas in certain nonmammalian species both MHC-I and APGs are polymorphic and coevolve within stable haplotypes. Coevolution was suggested as an ancestral gnathostome feature, presumably enabling only a single highly expressed classical MHC-I gene. In this view coevolution, while optimizing some aspects of adaptive immunity, would also limit its flexibility by preventing the expansion of classical MHC-I into a multigene family. However, some nonmammalian taxa, such as salamanders, have multiple highly expressed MHC-I genes, suggesting either that coevolution is relaxed or that it does not prevent the establishment of multigene MHC-I. To distinguish between these two alternatives, we use salamanders (30 species from 16 genera representing six families) to test, within a comparative framework, a major prediction of the coevolution hypothesis: the positive correlation between MHC-I and APG diversity. We found that MHC-I diversity explained both within-individual and species-wide diversity of two APGs, TAP1 and TAP2, supporting their coevolution with MHC-I, whereas no consistent effect was detected for the other three APGs (PSMB8, PSMB9, and TAPBP). Our results imply that although coevolution occurs in salamanders, it does not preclude the expansion of the MHC-I gene family. Contrary to the previous suggestions, nonmammalian vertebrates thus may be able to accommodate diverse selection pressures with flexibility granted by rapid expansion or contraction of the MHC-I family, while retaining the benefits of coevolution between MHC-I and TAPs.

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