Reconstructing an Ancestral Mammalian Immune Supercomplex from a Marsupial Major Histocompatibility Complex

The first sequenced marsupial genome promises to reveal unparalleled insights into mammalian evolution. We have used theMonodelphis domestica (gray short-tailed opossum) sequence to construct the first map of a marsupial major histocompatibility complex (MHC). The MHC is the most gene-dense region of the mammalian genome and is critical to immunity and reproductive success. The marsupial MHC bridges the phylogenetic gap between the complex MHC of eutherian mammals and the minimal essential MHC of birds. Here we show that the opossum MHC is gene dense and complex, as in humans, but shares more organizational features with non-mammals. The Class I genes have amplified within the Class II region, resulting in a unique Class I/II region. We present a model of the organization of the MHC in ancestral mammals and its elaboration during mammalian evolution. The opossum genome, together with other extant genomes, reveals the existence of an ancestral “immune supercomplex” that contained genes of both types of natural killer receptors together with antigen processing genes and MHC genes.

[1]  A Steinle,et al.  Activation of NK cells and T cells by NKG2D, a receptor for stress-inducible MICA. , 1999, Science.

[2]  J. Boss,et al.  A common set of factors control the expression of the MHC class II, invariant chain, and HLA-DM genes. , 1999 .

[3]  Michael J. Wilson,et al.  The genomic context of natural killer receptor extended gene families , 2001, Immunological reviews.

[4]  S. Beck,et al.  A genome-wide survey of Major Histocompatibility Complex (MHC) genes and their paralogues in zebrafish , 2005, BMC Genomics.

[5]  M. Flajnik,et al.  Two highly divergent ancient allelic lineages of the transporter associated with antigen processing (TAP) gene in Xenopus: further evidence for co‐evolution among MHC class I region genes , 2003, European journal of immunology.

[6]  M. Flajnik,et al.  Two ancient allelic lineages at the single classical class I locus in the Xenopus MHC. , 1999, Journal of immunology.

[7]  M. Kasahara,et al.  Comparative genomics of the Mill family: a rapidly evolving MHC class I gene family , 2004, European journal of immunology.

[8]  G. Trinchieri,et al.  OSCAR is an FcRγ-associated receptor that is expressed by myeloid cells and is involved in antigen presentation and activation of human dendritic cells , 2004 .

[9]  T. D. Schneider,et al.  Sequence logos: a new way to display consensus sequences. , 1990, Nucleic acids research.

[10]  Michael B Brenner,et al.  Characterization of two avian MHC-like genes reveals an ancient origin of the CD1 family. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[11]  G. Trinchieri,et al.  OSCAR is an FcRgamma-associated receptor that is expressed by myeloid cells and is involved in antigen presentation and activation of human dendritic cells. , 2004, Blood.

[12]  Greg Elgar,et al.  Fugu orthologues of human major histocompatibility complex genes: a genome survey , 2002, Immunogenetics.

[13]  M. Flajnik,et al.  Comparative genomics of the MHC: glimpses into the evolution of the adaptive immune system. , 2001, Immunity.

[14]  M. Takami,et al.  A Novel Member of the Leukocyte Receptor Complex Regulates Osteoclast Differentiation , 2002, The Journal of experimental medicine.

[15]  J. Trowsdale,et al.  Comparative genomics of major histocompatibility complexes , 2004, Immunogenetics.

[16]  J. Graves,et al.  Molecular characterization and evolution of X and Y-borne ATRX homologues in American marsupials , 2005, Chromosome Research.

[17]  K. Belov,et al.  Marsupial MHC class II beta genes are not orthologous to the eutherian beta gene families. , 2004, The Journal of heredity.

[18]  J. Trowsdale,et al.  Genetic and functional relationships between MHC and NK receptor genes. , 2001, Immunity.

[19]  M. Yamazaki,et al.  Genomic evolution of MHC class I region in primates. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[20]  S. Beck,et al.  Characterization of the Chicken C-Type Lectin-Like Receptors B-NK and B-lec Suggests That the NK Complex and the MHC Share a Common Ancestral Region1 , 2005, The Journal of Immunology.

[21]  E. Myers,et al.  Basic local alignment search tool. , 1990, Journal of molecular biology.

[22]  P. Jensen,et al.  Transcriptional regulation of the MHC class II antigen presentation pathway. , 2003, Current opinion in immunology.

[23]  K. Miska,et al.  Analysis of a marsupial MHC region containing two recently duplicated class I loci , 2004, Mammalian Genome.

[24]  J. Klein,et al.  Linkage of LMP, TAP, and RING3 with Mhc class I rather than class II genes in the zebrafish. , 1997, Journal of immunology.

[25]  W. J. Kent,et al.  BLAT--the BLAST-like alignment tool. , 2002, Genome research.

[26]  K. Belov,et al.  Marsupial MHC Class II β Genes Are Not Orthologous to the Eutherian β Gene Families , 2004 .

[27]  John Trowsdale,et al.  Features of MHC and NK gene clusters. , 2005, Transplant immunology.

[28]  J. Graves,et al.  Linkage mapping and physical localization of the major histocompatibility complex region of the marsupial Monodelphis domestica , 2006, Cytogenetic and Genome Research.

[29]  J. Kaufman,et al.  Two CD1 genes map to the chicken MHC, indicating that CD1 genes are ancient and likely to have been present in the primordial MHC. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[30]  S. O’Brien,et al.  The feline major histocompatibility complex is rearranged by an inversion with a breakpoint in the distal class I region , 2004, Immunogenetics.

[31]  J. Klein,et al.  Linkage of RXRB-like genes to class I and not to class II Mhc genes in the zebrafish , 1998, Immunogenetics.

[32]  M. Flajnik,et al.  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 Lineages1 , 2002, The Journal of Immunology.

[33]  C. Auffray,et al.  The chicken B locus is a minimal essential major histocompatibility complex , 1999, Nature.

[34]  J. Deakin,et al.  Characterizing the chromosomes of the Australian model marsupial Macropus eugenii (tammar wallaby) , 2005, Chromosome Research.

[35]  M. Nonaka,et al.  Comparative Genomics of Medaka: The Major Histocompatibility Complex (MHC) , 2001, Marine Biotechnology.

[36]  J. Kaufman,et al.  Co-evolving genes in MHC haplotypes: the "rule" for nonmammalian vertebrates? , 1999, Immunogenetics.

[37]  N. Shimizu,et al.  Unprecedented intraspecific diversity of the MHC class I region of a teleost medaka, Oryzias latipes , 2005, Immunogenetics.

[38]  S. Lewis,et al.  The generic genome browser: a building block for a model organism system database. , 2002, Genome research.

[39]  C. Amadou Evolution of the Mhc class I region: the framework hypothesis , 1999, Immunogenetics.

[40]  M. Flajnik,et al.  Major histocompatibility complex gene mapping in the amphibian Xenopus implies a primordial organization. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[41]  Toyoyuki Takada,et al.  Genomic organization of the mammalian MHC. , 2003, Annual review of immunology.

[42]  Michael J Benton,et al.  Dating the Tree of Life , 2003, Science.

[43]  C. Burge,et al.  Computational inference of homologous gene structures in the human genome. , 2001, Genome research.

[44]  N. Shimizu,et al.  Nucleotide sequence of the MHC class I genomic region of a teleost, the medaka (Oryzias latipes) , 2002, Immunogenetics.

[45]  S. Karlin,et al.  Prediction of complete gene structures in human genomic DNA. , 1997, Journal of molecular biology.

[46]  Gen Tamiya,et al.  Complete sequence and gene map of a human major histocompatibility complex , 1999 .

[47]  Elena S. Babaylova,et al.  Complete sequence and gene map of a human major histocompatibility complex , 1999, Nature.

[48]  Gary D. Stormo,et al.  DNA binding sites: representation and discovery , 2000, Bioinform..

[49]  K. Miska,et al.  Marsupial Mhc class I: classical sequences from the opossum, Monodelphis domestica , 1999, Immunogenetics.

[50]  M. Kasahara,et al.  A family of MHC class I-like genes located in the vicinity of the mouse leukocyte receptor complex , 2002, Proceedings of the National Academy of Sciences of the United States of America.

[51]  L. Hellman,et al.  Evolution of the major histocompatibility complex: Isolation of class II β cDNAs from two monotremes, the platypus and the short-beaked echidna , 2003, Immunogenetics.