Major histocompatibility complex (MHC) fragment numbers alone – in Atlantic cod and in general - do not represent functional variability

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...

Full description

Bibliographic Details
Published in:F1000Research
Main Authors: Dijkstra, Johannes M., Grimholt, Unni
Format: Text
Language:English
Published: F1000 Research Limited 2018
Subjects:
Online Access:http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6081975/
https://doi.org/10.12688/f1000research.15386.1
id ftpubmed:oai:pubmedcentral.nih.gov:6081975
record_format openpolar
spelling ftpubmed:oai:pubmedcentral.nih.gov:6081975 2023-05-15T15:27:45+02:00 Major histocompatibility complex (MHC) fragment numbers alone – in Atlantic cod and in general - do not represent functional variability Dijkstra, Johannes M. Grimholt, Unni 2018-06-28 http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6081975/ https://doi.org/10.12688/f1000research.15386.1 en eng F1000 Research Limited http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6081975/ http://dx.doi.org/10.12688/f1000research.15386.1 Copyright: © 2018 Dijkstra JM and Grimholt U http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. CC-BY Correspondence Text 2018 ftpubmed https://doi.org/10.12688/f1000research.15386.1 2018-08-26T00:09:39Z 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. 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. In addition, we explain 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. Text atlantic cod PubMed Central (PMC) F1000Research 7 963
institution Open Polar
collection PubMed Central (PMC)
op_collection_id ftpubmed
language English
topic Correspondence
spellingShingle Correspondence
Dijkstra, Johannes M.
Grimholt, Unni
Major histocompatibility complex (MHC) fragment numbers alone – in Atlantic cod and in general - do not represent functional variability
topic_facet Correspondence
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. 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. In addition, we explain 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 Text
author Dijkstra, Johannes M.
Grimholt, Unni
author_facet Dijkstra, Johannes M.
Grimholt, Unni
author_sort Dijkstra, Johannes M.
title Major histocompatibility complex (MHC) fragment numbers alone – in Atlantic cod and in general - do not represent functional variability
title_short Major histocompatibility complex (MHC) fragment numbers alone – in Atlantic cod and in general - do not represent functional variability
title_full Major histocompatibility complex (MHC) fragment numbers alone – in Atlantic cod and in general - do not represent functional variability
title_fullStr Major histocompatibility complex (MHC) fragment numbers alone – in Atlantic cod and in general - do not represent functional variability
title_full_unstemmed Major histocompatibility complex (MHC) fragment numbers alone – in Atlantic cod and in general - do not represent functional variability
title_sort major histocompatibility complex (mhc) fragment numbers alone – in atlantic cod and in general - do not represent functional variability
publisher F1000 Research Limited
publishDate 2018
url http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6081975/
https://doi.org/10.12688/f1000research.15386.1
genre atlantic cod
genre_facet atlantic cod
op_relation http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6081975/
http://dx.doi.org/10.12688/f1000research.15386.1
op_rights Copyright: © 2018 Dijkstra JM and Grimholt U
http://creativecommons.org/licenses/by/4.0/
This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
op_rightsnorm CC-BY
op_doi https://doi.org/10.12688/f1000research.15386.1
container_title F1000Research
container_volume 7
container_start_page 963
_version_ 1766358171726643200