Hox cluster organization in the jawless vertebrate Petromyzon marinus.

Large-scale gene amplifications may have facilitated the evolution of morphological innovations that accompanied the origin of vertebrates. This hypothesis predicts that the genomes of extant jawless fish, scions of deeply branching vertebrate lineages, should bear a record of these events. Previous work suggests that nonvertebrate chordates have a single Hox cluster, but that gnathostome vertebrates have four or more Hox clusters. Did the duplication events that produced multiple vertebrate Hox clusters occur before or after the divergence of agnathan and gnathostome lineages? Can investigation of lamprey Hox clusters illuminate the origins of the four gnathostome Hox clusters? To approach these questions, we cloned and sequenced 13 Hox cluster genes from cDNA and genomic libraries in the lamprey, Petromyzon marinus. The results suggest that the lamprey has at least four Hox clusters and support the model that gnathostome Hox clusters arose by a two-round-no-cluster-loss mechanism, with tree topology [(AB)(CD)]. A three-round model, however, is not rigorously excluded by the data and, for this model, the tree topologies [(D(C(AB))] and [(C(D(AB))] are most parsimonious. Gene phylogenies suggest that at least one Hox cluster duplication occurred in the lamprey lineage after it diverged from the gnathostome lineage. The results argue against two or more rounds of duplication before the divergence of agnathan and gnathostome vertebrates. If Hox clusters were duplicated in whole-genome duplication events, then these data suggest that, at most, one whole genome duplication occurred before the evolution of vertebrate developmental innovations.

[1]  J. Piatigorsky,et al.  The recruitment of crystallins: new functions precede gene duplication , 1991, Science.

[2]  P. Holland,et al.  Hox genes and chordate evolution. , 1996, Developmental biology.

[3]  N. Saitou,et al.  The neighbor-joining method: a new method for reconstructing phylogenetic trees. , 1987, Molecular biology and evolution.

[4]  R. Krumlauf,et al.  Conservation and elaboration of Hox gene regulation during evolution of the vertebrate head , 2000, Nature.

[5]  P. Holland,et al.  Colinear and segmental expression of amphioxus Hox genes. , 1999, Developmental biology.

[6]  J. Langeland,et al.  Lamprey Dlx genes and early vertebrate evolution. , 2001, Proceedings of the National Academy of Sciences of the United States of America.

[7]  E. Davidson,et al.  Organization of an echinoderm Hox gene cluster. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[8]  A. Meyer,et al.  Gene and genome duplications in vertebrates: the one-to-four (-to-eight in fish) rule and the evolution of novel gene functions. , 1999, Current opinion in cell biology.

[9]  Jordi Garcia-Fernàndez,et al.  Archetypal organization of the amphioxus Hox gene cluster , 1994, Nature.

[10]  E. Lewis A gene complex controlling segmentation in Drosophila , 1978, Nature.

[11]  W Miller,et al.  Hox cluster genomics in the horn shark, Heterodontus francisci. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[12]  L. Joly,et al.  Zebrafish hox genes: genomic organization and modified colinear expression patterns in the trunk. , 1998, Development.

[13]  P. Holland,et al.  The amphioxus Hox cluster: deuterostome posterior flexibility and Hox14 , 2000, Evolution & development.

[14]  T J Gibson,et al.  Evidence in favour of ancient octaploidy in the vertebrate genome. , 2000, Biochemical Society transactions.

[15]  K. Katoh,et al.  Protein Tyrosine Kinase cDNAs from Amphioxus, Hagfish, and Lamprey: Isoform Duplications Around the Divergence of Cyclostomes and Gnathostomes , 1999, Journal of Molecular Evolution.

[16]  D. Duboule Guidebook to the homeobox genes , 1994 .

[17]  HOX Gene Links Limb, Genital Defects , 1997, Science.

[18]  B. Efron,et al.  A Leisurely Look at the Bootstrap, the Jackknife, and , 1983 .

[19]  W. McGinnis,et al.  A century of homeosis, a decade of homeoboxes. , 1994, Genetics.

[20]  L. Lundin,et al.  Evolution of the vertebrate genome as reflected in paralogous chromosomal regions in man and the house mouse. , 1993, Genomics.

[21]  Todd H. Oakley,et al.  Reconstructing ancestral character states: a critical reappraisal. , 1998, Trends in ecology & evolution.

[22]  G. Wagner,et al.  PCR-survey of Hox-genes of the zebrafish: new sequence information and evolutionary implications. , 1996, The Journal of experimental zoology.

[23]  M. Kondo,et al.  A detailed linkage map of medaka, Oryzias latipes: comparative genomics and genome evolution. , 2000, Genetics.

[24]  Austin L. Hughes,et al.  Phylogenies of Developmentally Important Proteins Do Not Support the Hypothesis of Two Rounds of Genome Duplication Early in Vertebrate History , 1999, Journal of Molecular Evolution.

[25]  J. Spring,et al.  Vertebrate evolution by interspecific hybridisation – are we polyploid? , 1997, FEBS letters.

[26]  J. W. Pendleton,et al.  Expansion of the Hox gene family and the evolution of chordates. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[27]  A. Abzhanov,et al.  Homeotic genes and the arthropod head: expression patterns of the labial, proboscipedia, and Deformed genes in crustaceans and insects. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[28]  K. Katoh,et al.  Monophyly of Lampreys and Hagfishes Supported by Nuclear DNA–Coded Genes , 1999, Journal of Molecular Evolution.

[29]  A. Hughes,et al.  Ancient genome duplications did not structure the human Hox-bearing chromosomes. , 2001, Genome research.

[30]  William McGinnis,et al.  Homeobox genes and axial patterning , 1992, Cell.

[31]  M. Nei,et al.  Evolution of Antennapedia-class homeobox genes. , 1996, Genetics.

[32]  W. Gehring,et al.  Homeobox genes in the ribbonworm Lineus sanguineus: evolutionary implications. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[33]  A. Sidow Gen(om)e duplications in the evolution of early vertebrates. , 1996, Current opinion in genetics & development.

[34]  Dr. Susumu Ohno Evolution by Gene Duplication , 1970, Springer Berlin Heidelberg.

[35]  M. Martindale,et al.  Conserved anterior boundaries of Hox gene expression in the central nervous system of the leech Helobdella. , 1997, Developmental biology.

[36]  J. Langeland,et al.  Otx expression during lamprey embryogenesis provides insights into the evolution of the vertebrate head and jaw. , 1999, Developmental biology.

[37]  J. Langeland,et al.  islet reveals segmentation in the Amphioxus hindbrain homolog. , 2000, Developmental biology.

[38]  S. Aizawa,et al.  Otx cognates in a lamprey, Lampetra japonica , 1998, Development Genes and Evolution.

[39]  J. Felsenstein CONFIDENCE LIMITS ON PHYLOGENIES: AN APPROACH USING THE BOOTSTRAP , 1985, Evolution; international journal of organic evolution.

[40]  S. Morris,et al.  Lower Cambrian vertebrates from south China , 1999, Nature.

[41]  P. Holland,et al.  Evidence for 14 homeobox gene clusters in human genome ancestry , 2000, Current Biology.

[42]  Nobuyoshi Shimizu,et al.  Genomic analysis of Hox clusters in the sea lamprey Petromyzon marinus. , 2002, The Journal of experimental zoology.

[43]  Byrappa Venkatesh,et al.  Organization of the Fugu rubripes Hox clusters: evidence for continuing evolution of vertebrate Hox complexes , 1997, Nature Genetics.

[44]  R. Krumlauf Hox genes in vertebrate development , 1994, Cell.

[45]  Y L Wang,et al.  Zebrafish hox clusters and vertebrate genome evolution. , 1998, Science.

[46]  K. H. Wolfe Yesterday's polyploids and the mystery of diploidization , 2001, Nature Reviews Genetics.

[47]  C. Cunningham Some Limitations of Ancestral Character-State Reconstruction When Testing Evolutionary Hypotheses , 1999 .

[48]  M. Schummer,et al.  Evolution of Antp-class genes and differential expression of Hydra Hox/paraHox genes in anterior patterning. , 2000, Proceedings of the National Academy of Sciences of the United States of America.

[49]  A. Force,et al.  The probability of duplicate gene preservation by subfunctionalization. , 2000, Genetics.

[50]  J. Eisen,et al.  Development of the neural crest in the zebrafish. , 1993, Developmental biology.

[51]  J. Piatigorsky,et al.  Multifunctional Lens Crystallins and Corneal Enzymes: More than Meets the Eye , 1998, Annals of the New York Academy of Sciences.

[52]  L. Holland,et al.  Evolution of neural crest and placodes: amphioxus as a model for the ancestral vertebrate? , 2001, Journal of anatomy.

[53]  C. Gans,et al.  The Genesis of Neural Crest and Epidermal Placodes: A Reinterpretation of Vertebrate Origins , 1983, The Quarterly Review of Biology.

[54]  C. Kappen,et al.  Evolution of a regulatory gene family: HOM/HOX genes. , 1993, Current opinion in genetics & development.

[55]  A. Spagnuolo,et al.  Cloning of ascidian homeobox genes provides evidence for a primordial chordate cluster. , 1995, Gene.

[56]  G. Wagner,et al.  Phylogenetic reconstruction of vertebrate Hox cluster duplications. , 1997, Molecular biology and evolution.

[57]  J. Garcia-Fernández,et al.  Amphioxus Evx genes: implications for the evolution of the Midbrain-Hindbrain Boundary and the chordate tailbud. , 2001, Developmental biology.

[58]  C Kappen,et al.  Duplication of large genomic regions during the evolution of vertebrate homeobox genes. , 1989, Proceedings of the National Academy of Sciences of the United States of America.

[59]  F. Ruddle,et al.  Molecular evolution of Hox gene regulation: cloning and transgenic analysis of the lamprey HoxQ8 gene. , 1998, The Journal of experimental zoology.

[60]  A. Force,et al.  Preservation of duplicate genes by complementary, degenerative mutations. , 1999, Genetics.

[61]  G. Wagner,et al.  Evolution of Chordate Hox Gene Clusters a , 1999, Annals of the New York Academy of Sciences.

[62]  P. Holland,et al.  Estimation of Hox gene cluster number in lampreys. , 1998, The International journal of developmental biology.