Major histocompatibility complex (MHC) fragment numbers alone – in Atlantic cod and in general - do not represent functional variability [version 2; referees: 2 approved, 1 approved with reservations]

This correspondence concerns a publication by Malmstrøm et al. in Nature Genetics in October 2016. Malmstrøm et al. made an important contribution to fish phylogeny research by using low-coverage genome sequencing for comparison of 66 teleost (modern bony) fish species, with 64 of those 66 belonging...

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Published in:F1000Research
Main Authors: Johannes M. Dijkstra, Unni Grimholt
Format: Article in Journal/Newspaper
Language:English
Published: F1000 Research Ltd 2018
Subjects:
R
Q
Online Access:https://doi.org/10.12688/f1000research.15386.2
https://doaj.org/article/4b0056cdca2544c58456dc0c5e8dee2c
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spelling ftdoajarticles:oai:doaj.org/article:4b0056cdca2544c58456dc0c5e8dee2c 2023-05-15T15:27:49+02:00 Major histocompatibility complex (MHC) fragment numbers alone – in Atlantic cod and in general - do not represent functional variability [version 2; referees: 2 approved, 1 approved with reservations] Johannes M. Dijkstra Unni Grimholt 2018-09-01T00:00:00Z https://doi.org/10.12688/f1000research.15386.2 https://doaj.org/article/4b0056cdca2544c58456dc0c5e8dee2c EN eng F1000 Research Ltd https://f1000research.com/articles/7-963/v2 https://doaj.org/toc/2046-1402 2046-1402 doi:10.12688/f1000research.15386.2 https://doaj.org/article/4b0056cdca2544c58456dc0c5e8dee2c F1000Research, Vol 7 (2018) Medicine R Science Q article 2018 ftdoajarticles https://doi.org/10.12688/f1000research.15386.2 2022-12-31T02:32:46Z This correspondence concerns a publication by Malmstrøm et al. in Nature Genetics in October 2016. Malmstrøm et al. made an important contribution to fish phylogeny research by using low-coverage genome sequencing for comparison of 66 teleost (modern bony) fish species, with 64 of those 66 belonging to the species-rich clade Neoteleostei, and with 27 of those 64 belonging to the order Gadiformes. For these 66 species, Malmstrøm et al. estimated numbers of genes belonging to the major histocompatibility complex (MHC) class I lineages U and Z and concluded that in teleost fish these combined numbers are positively associated with, and a driving factor of, the rates of establishment of new fish species (speciation rates). They also claimed that functional genes for the MHC class II system molecules MHC IIA, MHC IIB, CD4 and CD74 were lost in early Gadiformes. Our main criticisms are (1) that the authors did not provide sufficient evidence for presence or absence of intact functional MHC class I or MHC class II system genes, (2) that they did not discuss that an MHC subpopulation gene number alone is a very incomplete measure of MHC variance, and (3) that the MHC system is more likely to reduce speciation rates than to enhance them. Furthermore, their use of the Ornstein-Uhlenbeck model is a typical example of overly naïve use of that model system. In short, we conclude that their new model of MHC class I evolution, reflected in their title “Evolution of the immune system influences speciation rates in teleost fish”, is unsubstantiated, and that their “pinpointing” of the functional loss of the MHC class II system and all the important MHC class II system genes to the onset of Gadiformes is preliminary, because they did not sufficiently investigate the species at the clade border. Article in Journal/Newspaper atlantic cod Directory of Open Access Journals: DOAJ Articles F1000Research 7 963
institution Open Polar
collection Directory of Open Access Journals: DOAJ Articles
op_collection_id ftdoajarticles
language English
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Johannes M. Dijkstra
Unni Grimholt
Major histocompatibility complex (MHC) fragment numbers alone – in Atlantic cod and in general - do not represent functional variability [version 2; referees: 2 approved, 1 approved with reservations]
topic_facet Medicine
R
Science
Q
description This correspondence concerns a publication by Malmstrøm et al. in Nature Genetics in October 2016. Malmstrøm et al. made an important contribution to fish phylogeny research by using low-coverage genome sequencing for comparison of 66 teleost (modern bony) fish species, with 64 of those 66 belonging to the species-rich clade Neoteleostei, and with 27 of those 64 belonging to the order Gadiformes. For these 66 species, Malmstrøm et al. estimated numbers of genes belonging to the major histocompatibility complex (MHC) class I lineages U and Z and concluded that in teleost fish these combined numbers are positively associated with, and a driving factor of, the rates of establishment of new fish species (speciation rates). They also claimed that functional genes for the MHC class II system molecules MHC IIA, MHC IIB, CD4 and CD74 were lost in early Gadiformes. Our main criticisms are (1) that the authors did not provide sufficient evidence for presence or absence of intact functional MHC class I or MHC class II system genes, (2) that they did not discuss that an MHC subpopulation gene number alone is a very incomplete measure of MHC variance, and (3) that the MHC system is more likely to reduce speciation rates than to enhance them. Furthermore, their use of the Ornstein-Uhlenbeck model is a typical example of overly naïve use of that model system. In short, we conclude that their new model of MHC class I evolution, reflected in their title “Evolution of the immune system influences speciation rates in teleost fish”, is unsubstantiated, and that their “pinpointing” of the functional loss of the MHC class II system and all the important MHC class II system genes to the onset of Gadiformes is preliminary, because they did not sufficiently investigate the species at the clade border.
format Article in Journal/Newspaper
author Johannes M. Dijkstra
Unni Grimholt
author_facet Johannes M. Dijkstra
Unni Grimholt
author_sort Johannes M. Dijkstra
title Major histocompatibility complex (MHC) fragment numbers alone – in Atlantic cod and in general - do not represent functional variability [version 2; referees: 2 approved, 1 approved with reservations]
title_short Major histocompatibility complex (MHC) fragment numbers alone – in Atlantic cod and in general - do not represent functional variability [version 2; referees: 2 approved, 1 approved with reservations]
title_full Major histocompatibility complex (MHC) fragment numbers alone – in Atlantic cod and in general - do not represent functional variability [version 2; referees: 2 approved, 1 approved with reservations]
title_fullStr Major histocompatibility complex (MHC) fragment numbers alone – in Atlantic cod and in general - do not represent functional variability [version 2; referees: 2 approved, 1 approved with reservations]
title_full_unstemmed Major histocompatibility complex (MHC) fragment numbers alone – in Atlantic cod and in general - do not represent functional variability [version 2; referees: 2 approved, 1 approved with reservations]
title_sort major histocompatibility complex (mhc) fragment numbers alone – in atlantic cod and in general - do not represent functional variability [version 2; referees: 2 approved, 1 approved with reservations]
publisher F1000 Research Ltd
publishDate 2018
url https://doi.org/10.12688/f1000research.15386.2
https://doaj.org/article/4b0056cdca2544c58456dc0c5e8dee2c
genre atlantic cod
genre_facet atlantic cod
op_source F1000Research, Vol 7 (2018)
op_relation https://f1000research.com/articles/7-963/v2
https://doaj.org/toc/2046-1402
2046-1402
doi:10.12688/f1000research.15386.2
https://doaj.org/article/4b0056cdca2544c58456dc0c5e8dee2c
op_doi https://doi.org/10.12688/f1000research.15386.2
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