Literature DB >> 11777971

Proteasome, transporter associated with antigen processing, and class I genes in the nurse shark Ginglymostoma cirratum: evidence for a stable class I region and MHC haplotype lineages.

Yuko Ohta1, E Churchill McKinney, Michael F Criscitiello, Martin F Flajnik.   

Abstract

Cartilaginous fish (e.g., sharks) are derived from the oldest vertebrate ancestor having an adaptive immune system, and thus are key models for examining MHC evolution. Previously, family studies in two shark species showed that classical class I (UAA) and class II genes are genetically linked. In this study, we show that proteasome genes LMP2 and LMP7, shark-specific LMP7-like, and the TAP1/2 genes are linked to class I/II. Functional LMP7 and LMP7-like genes, as well as multiple LMP2 genes or gene fragments, are found only in some sharks, suggesting that different sets of peptides might be generated depending upon inherited MHC haplotypes. Cosmid clones bearing the MHC-linked classical class I genes were isolated and shown to contain proteasome gene fragments. A non-MHC-linked LMP7 gene also was identified on another cosmid, but only two exons of this gene were detected, closely linked to a class I pseudogene (UAA-NC2); this region probably resulted from a recent duplication and translocation from the functional MHC. Tight linkage of proteasome and class I genes, in comparison with gene organizations of other vertebrates, suggests a primordial MHC organization. Another nonclassical class I gene (UAA-NC1) was detected that is linked neither to MHC nor to UAA-NC2; its high level of sequence similarity to UAA suggests that UAA-NC1 also was recently derived from UAA and translocated from MHC. These data further support the principle of a primordial class I region with few class I genes. Finally, multiple paternities in one family were demonstrated, with potential segregation distortions.

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Year:  2002        PMID: 11777971      PMCID: PMC7039333          DOI: 10.4049/jimmunol.168.2.771

Source DB:  PubMed          Journal:  J Immunol        ISSN: 0022-1767            Impact factor:   5.422


  54 in total

Review 1.  The proteasome.

Authors:  M Bochtler; L Ditzel; M Groll; C Hartmann; R Huber
Journal:  Annu Rev Biophys Biomol Struct       Date:  1999

2.  Gene organization of the quail major histocompatibility complex (MhcCoja) class I gene region.

Authors:  T Shiina; C Shimizu; A Oka; Y Teraoka; T Imanishi; T Gojobori; K Hanzawa; S Watanabe; H Inoko
Journal:  Immunogenetics       Date:  1999-05       Impact factor: 2.846

3.  Isolation of Mhc class I cDNAs from the axolotl Ambystoma mexicanum.

Authors:  B Sammut; V Laurens; A Tournefier
Journal:  Immunogenetics       Date:  1997       Impact factor: 2.846

4.  Isolation of low molecular mass polypeptide complementary DNA clones from primitive vertebrates. Implications for the origin of MHC class I-restricted antigen presentation.

Authors:  E Kandil; C Namikawa; M Nonaka; A S Greenberg; M F Flajnik; T Ishibashi; M Kasahara
Journal:  J Immunol       Date:  1996-06-01       Impact factor: 5.422

5.  Identification of class I genes in cartilaginous fish, the most ancient group of vertebrates displaying an adaptive immune response.

Authors:  S Bartl; M A Baish; M F Flajnik; Y Ohta
Journal:  J Immunol       Date:  1997-12-15       Impact factor: 5.422

6.  Class I mhc genes of cichlid fishes: identification, expression, and polymorphism.

Authors:  A Sato; D Klein; H Sültmann; F Figueroa; C O'hUigin; J Klein
Journal:  Immunogenetics       Date:  1997       Impact factor: 2.846

7.  MHC-linked LMP gene products specifically alter peptidase activities of the proteasome.

Authors:  J Driscoll; M G Brown; D Finley; J J Monaco
Journal:  Nature       Date:  1993-09-16       Impact factor: 49.962

8.  Two ancient allelic lineages at the single classical class I locus in the Xenopus MHC.

Authors:  M F Flajnik; Y Ohta; A S Greenberg; L Salter-Cid; A Carrizosa; L Du Pasquier; M Kasahara
Journal:  J Immunol       Date:  1999-10-01       Impact factor: 5.422

9.  Mapping of mhc class I and class II regions to different linkage groups in the zebrafish, Danio rerio.

Authors:  J Bingulac-Popovic; F Figueroa; A Sato; W S Talbot; S L Johnson; M Gates; J H Postlethwait; J Klein
Journal:  Immunogenetics       Date:  1997       Impact factor: 2.846

10.  Characterization of the MHC class I region of the Japanese pufferfish (Fugu rubripes).

Authors:  M S Clark; L Shaw; A Kelly; P Snell; G Elgar
Journal:  Immunogenetics       Date:  2001       Impact factor: 2.846

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  31 in total

1.  Physical and genetic mapping of the rainbow trout major histocompatibility regions: evidence for duplication of the class I region.

Authors:  Ruth B Phillips; Ana Zimmerman; Marc A Noakes; Yniv Palti; Matt R W Morasch; Lisa Eiben; Sandra S Ristow; Gary H Thorgaard; John D Hansen
Journal:  Immunogenetics       Date:  2003-10-18       Impact factor: 2.846

2.  Evolutionary analysis of two classical MHC class I loci of the medaka fish, Oryzias latipes: haplotype-specific genomic diversity, locus-specific polymorphisms, and interlocus homogenization.

Authors:  Mayumi I Nonaka; Masaru Nonaka
Journal:  Immunogenetics       Date:  2010-02-20       Impact factor: 2.846

3.  Transspecies dimorphic allelic lineages of the proteasome subunit beta-type 8 gene (PSMB8) in the teleost genus Oryzias.

Authors:  Fumi Miura; Kentaro Tsukamoto; Ratnesh Bhai Mehta; Kiyoshi Naruse; Wichian Magtoon; Masaru Nonaka
Journal:  Proc Natl Acad Sci U S A       Date:  2010-11-23       Impact factor: 11.205

4.  Dimorphisms of the proteasome subunit beta type 8 gene (PSMB8) of ectothermic tetrapods originated in multiple independent evolutionary events.

Authors:  Ching-Huei Huang; Yuta Tanaka; Naoko T Fujito; Masaru Nonaka
Journal:  Immunogenetics       Date:  2013-08-28       Impact factor: 2.846

5.  Polymorphism, natural selection, and structural modeling of class Ia MHC in the African clawed frog (Xenopus laevis).

Authors:  D H Bos; B Waldman
Journal:  Immunogenetics       Date:  2006-04-28       Impact factor: 2.846

Review 6.  Origin and evolution of the specialized forms of proteasomes involved in antigen presentation.

Authors:  Masanori Kasahara; Martin F Flajnik
Journal:  Immunogenetics       Date:  2019-01-24       Impact factor: 2.846

7.  Alternative haplotypes of antigen processing genes in zebrafish diverged early in vertebrate evolution.

Authors:  Sean C McConnell; Kyle M Hernandez; Dustin J Wcisel; Ross N Kettleborough; Derek L Stemple; Jeffrey A Yoder; Jorge Andrade; Jill L O de Jong
Journal:  Proc Natl Acad Sci U S A       Date:  2016-08-04       Impact factor: 11.205

Review 8.  Coevolution of MHC genes (LMP/TAP/class Ia, NKT-class Ib, NKp30-B7H6): lessons from cold-blooded vertebrates.

Authors:  Yuko Ohta; Martin F Flajnik
Journal:  Immunol Rev       Date:  2015-09       Impact factor: 12.988

9.  Comparative genomic analysis of the major histocompatibility complex class I region in the teleost genus Oryzias.

Authors:  Ratnesh Bhai Mehta; Mayumi I Nonaka; Masaru Nonaka
Journal:  Immunogenetics       Date:  2009-04-07       Impact factor: 2.846

10.  MHC-linked and un-linked class I genes in the wallaby.

Authors:  Hannah V Siddle; Janine E Deakin; Penny Coggill; Elizabeth Hart; Yuanyuan Cheng; Emily Sw Wong; Jennifer Harrow; Stephan Beck; Katherine Belov
Journal:  BMC Genomics       Date:  2009-07-14       Impact factor: 3.969

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