Subfunctionalization of Duplicated Zebrafish pax6 Genes by cis-Regulatory Divergence

Gene duplication is a major driver of evolutionary divergence. In most vertebrates a single PAX6 gene encodes a transcription factor required for eye, brain, olfactory system, and pancreas development. In zebrafish, following a postulated whole-genome duplication event in an ancestral teleost, duplicates pax6a and pax6b jointly fulfill these roles. Mapping of the homozygously viable eye mutant sunrise identified a homeodomain missense change in pax6b, leading to loss of target binding. The mild phenotype emphasizes role-sharing between the co-orthologues. Meticulous mapping of isolated BACs identified perturbed synteny relationships around the duplicates. This highlights the functional conservation of pax6 downstream (3′) control sequences, which in most vertebrates reside within the introns of a ubiquitously expressed neighbour gene, ELP4, whose pax6a-linked exons have been lost in zebrafish. Reporter transgenic studies in both mouse and zebrafish, combined with analysis of vertebrate sequence conservation, reveal loss and retention of specific cis-regulatory elements, correlating strongly with the diverged expression of co-orthologues, and providing clear evidence for evolution by subfunctionalization.

[1]  G. Tell,et al.  A molecular code dictates sequence‐specific DNA recognition by homeodomains. , 1996, The EMBO journal.

[2]  Melina E. Hale,et al.  Duplication events and the evolution of segmental identity , 2005, Evolution & development.

[3]  S. Herzig,et al.  Tissue-specific transcriptional activity of a pancreatic islet cell-specific enhancer sequence/Pax6-binding site determined in normal adult tissues in vivo using transgenic mice. , 1999, Molecular endocrinology.

[4]  J. Crolla,et al.  Frequent chromosome aberrations revealed by molecular cytogenetic studies in patients with aniridia. , 2002, American journal of human genetics.

[5]  P. Gruss,et al.  Conditional inactivation of Pax6 in the pancreas causes early onset of diabetes. , 2004, Developmental biology.

[6]  R. Strauss,et al.  Drosophila Pax-6/eyeless is essential for normal adult brain structure and function. , 2001, Journal of neurobiology.

[7]  D. Duboule,et al.  Mouse limb deformity mutations disrupt a global control region within the large regulatory landscape required for Gremlin expression. , 2004, Genes & development.

[8]  J. Lauderdale,et al.  Analysis of Pax6 expression using a BAC transgene reveals the presence of a paired-less isoform of Pax6 in the eye and olfactory bulb. , 2006, Developmental biology.

[9]  G. Saunders,et al.  Mouse Small eye results from mutations in a paired-like homeobox-containing gene , 1991, Nature.

[10]  R. Maas,et al.  Genomic structure, evolutionary conservation and aniridia mutations in the human PAX6 gene , 1992, Nature Genetics.

[11]  Samantha L. Free,et al.  PAX6 haploinsufficiency causes cerebral malformation and olfactory dysfunction in humans , 2001, Nature Genetics.

[12]  A. Cvekl,et al.  Functional properties of natural human PAX6 and PAX6(5a) mutants. , 2004, Investigative ophthalmology & visual science.

[13]  Richard L. Maas,et al.  Regulation of Pax6 expression is conserved between mice and flies. , 1999, Development.

[14]  P. Gruss,et al.  Pax6 activity in the lens primordium is required for lens formation and for correct placement of a single retina in the eye. , 2000, Genes & development.

[15]  M. Zannini,et al.  Multiple mechanisms of interference between transformation and differentiation in thyroid cells , 1992, Molecular and cellular biology.

[16]  Justin Johnson,et al.  Ancient Noncoding Elements Conserved in the Human Genome , 2006, Science.

[17]  Peter Nürnberg,et al.  Three novel Pax6 alleles in the mouse leading to the same small-eye phenotype caused by different consequences at target promoters. , 2005, Investigative ophthalmology & visual science.

[18]  Y. Fukushima,et al.  Aniridia-associated cytogenetic rearrangements suggest that a position effect may cause the mutant phenotype. , 1995, Human molecular genetics.

[19]  James Taylor Clues to function in gene deserts. , 2005, Trends in biotechnology.

[20]  G. Elgar,et al.  Comparative genomics using Fugu reveals insights into regulatory subfunctionalization , 2007, Genome Biology.

[21]  Edward M. Rubin,et al.  Deletion of a coordinate regulator of type 2 cytokine expression in mice , 2001, Nature Immunology.

[22]  Andrew G. Clark,et al.  Evolutionary changes in cis and trans gene regulation , 2004, Nature.

[23]  A. Childs,et al.  Conserved elements in Pax6 intron 7 involved in (auto)regulation and alternative transcription. , 2004, Developmental biology.

[24]  D. Ovcharenko,et al.  Genomic deletion of a long-range bone enhancer misregulates sclerostin in Van Buchem disease. , 2005, Genome research.

[25]  S. Ekker,et al.  Effective targeted gene ‘knockdown’ in zebrafish , 2000, Nature Genetics.

[26]  D. Kleinjan,et al.  Long-range control of gene expression: emerging mechanisms and disruption in disease. , 2005, American journal of human genetics.

[27]  R. Lang,et al.  The upstream ectoderm enhancer in Pax6 has an important role in lens induction. , 2001, Development.

[28]  Alan M. Moses,et al.  In vivo enhancer analysis of human conserved non-coding sequences , 2006, Nature.

[29]  J A Epstein,et al.  Two independent and interactive DNA-binding subdomains of the Pax6 paired domain are regulated by alternative splicing. , 1994, Genes & development.

[30]  S. Saule,et al.  High conservation of cis-regulatory elements between quail and human for the Pax-6 gene , 1999, Development Genes and Evolution.

[31]  W. Bickmore,et al.  The reticulocalbin gene maps to the WAGR region in human and to the Small eye Harwell deletion in mouse. , 1997, Genomics.

[32]  V. van Heyningen,et al.  PAX6 in sensory development. , 2002, Human molecular genetics.

[33]  I. Tzoulaki,et al.  PAX6 mutations: genotype-phenotype correlations , 2005, BMC Genetics.

[34]  S. Fisher,et al.  Evaluating the biological relevance of putative enhancers using Tol2 transposon-mediated transgenesis in zebrafish , 2006, Nature Protocols.

[35]  T. Rosenberg,et al.  Mutational analysis of PAX6: 16 novel mutations including 5 missense mutations with a mild aniridia phenotype , 1999, European Journal of Human Genetics.

[36]  C. Desplan,et al.  Cooperative dimerization of paired class homeo domains on DNA. , 1993, Genes & development.

[37]  T. Ian Simpson,et al.  Long-range downstream enhancers are essential for Pax6 expression , 2006, Developmental biology.

[38]  C. Plessy,et al.  Enhancer sequence conservation between vertebrates is favoured in developmental regulator genes. , 2005, Trends in genetics : TIG.

[39]  P. Yeyati,et al.  Hsp90 Selectively Modulates Phenotype in Vertebrate Development , 2007, PLoS genetics.

[40]  J. Postlethwait,et al.  Structure of the zebrafish snail1 gene and its expression in wild-type, spadetail and no tail mutant embryos. , 1993, Development.

[41]  A. Schier,et al.  Inactivation of dispatched 1 by the chameleon mutation disrupts Hedgehog signalling in the zebrafish embryo. , 2004, Developmental biology.

[42]  K. Howe,et al.  Genomic regulatory blocks encompass multiple neighboring genes and maintain conserved synteny in vertebrates. , 2007, Genome research.

[43]  R. Tjian,et al.  Transcription regulation and animal diversity , 2003, Nature.

[44]  I. Gorlov,et al.  PAX6, Paired Domain Influences Sequence Recognition by the Homeodomain* , 2002, The Journal of Biological Chemistry.

[45]  John H Postlethwait,et al.  The zebrafish gene map defines ancestral vertebrate chromosomes. , 2005, Genome research.

[46]  J. Volff Genome evolution and biodiversity in teleost fish , 2005, Heredity.

[47]  David J. Price,et al.  The transcription factor Pax6 is required for development of the diencephalic dorsal midline secretory radial glia that form the subcommissural organ , 2001, Mechanisms of Development.

[48]  B. Doe,et al.  New 3′ elements control Pax6 expression in the developing pretectum, neural retina and olfactory region , 2002, Mechanisms of Development.

[49]  W. Gehring,et al.  Homology of the eyeless gene of Drosophila to the Small eye gene in mice and Aniridia in humans. , 1994, Science.

[50]  S. Prabhakar,et al.  Annotation of cis-regulatory elements by identification, subclassification, and functional assessment of multispecies conserved sequences. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[51]  R. Lang,et al.  A highly conserved lens transcriptional control element from the Pax-6 gene , 1998, Mechanisms of Development.

[52]  Axel Visel,et al.  Enhancer identification through comparative genomics. , 2006, Seminars in cell & developmental biology.

[53]  R. Axton,et al.  Missense mutations in the most ancient residues of the PAX6 paired domain underlie a spectrum of human congenital eye malformations. , 1999, Human molecular genetics.

[54]  H. Baier,et al.  A radiation hybrid map of the zebrafish genome , 1999, Nature Genetics.

[55]  H. Peters,et al.  Molecular Characterization of Pax 62 Neu Through Pax 610 Neu : An Extension of the Pax 6 Allelic Series and the Identification of Two Possible Hypomorph Alleles in the Mouse Mus musculus , 2001 .

[56]  Klaudia Walter,et al.  Highly Conserved Non-Coding Sequences Are Associated with Vertebrate Development , 2004, PLoS biology.

[57]  G. Elgar,et al.  Complete sequencing of the Fugu WAGR region from WT1 to PAX6: dramatic compaction and conservation of synteny with human chromosome 11p13. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[58]  Maximilian Muenke,et al.  A functional screen for sonic hedgehog regulatory elements across a 1 Mb interval identifies long-range ventral forebrain enhancers , 2006, Development.

[59]  Pawel Stankiewicz,et al.  Genomic Disorders: Molecular Mechanisms for Rearrangements and Conveyed Phenotypes , 2005, PLoS genetics.

[60]  P. Rashbass,et al.  Influence of PAX6 Gene Dosage on Development: Overexpression Causes Severe Eye Abnormalities , 1996, Cell.

[61]  Steve D. M. Brown,et al.  Novel ENU-induced eye mutations in the mouse: models for human eye disease. , 2002, Human molecular genetics.

[62]  G. Elgar,et al.  Characterization of a novel gene adjacent to PAX6, revealing synteny conservation with functional significance , 2002, Mammalian Genome.

[63]  W. Li,et al.  Isolation and expression of a Pax-6 gene in the regenerating and intact Planarian Dugesia(G)tigrina. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[64]  S. Saule,et al.  Pax-6 and Cdx-2/3 Interact to Activate Glucagon Gene Expression on the G1 Control Element* , 1999, The Journal of Biological Chemistry.

[65]  R. Gibbs,et al.  PipMaker--a web server for aligning two genomic DNA sequences. , 2000, Genome research.

[66]  D. Haussler,et al.  Ultraconserved Elements in the Human Genome , 2004, Science.

[67]  Richard L. Maas,et al.  PAX6 gene dosage effect in a family with congenital cataracts, aniridia, anophthalmia and central nervous system defects , 1994, Nature Genetics.

[68]  Volff Jn Genome evolution and biodiversity in teleost fish , 2005 .

[69]  J. Volff,et al.  Identification and comparative expression analysis of a second wt1 gene in zebrafish , 2006, Developmental dynamics : an official publication of the American Association of Anatomists.

[70]  Tanya Vavouri,et al.  Ancient duplicated conserved noncoding elements in vertebrates: a genomic and functional analysis. , 2006, Genome research.

[71]  Lior Pachter,et al.  VISTA: computational tools for comparative genomics , 2004, Nucleic Acids Res..

[72]  John D West,et al.  Controlled overexpression of Pax6 in vivo negatively autoregulates the Pax6 locus, causing cell-autonomous defects of late cortical progenitor proliferation with little effect on cortical arealization , 2006, Development.

[73]  M. Götz,et al.  Molecular dissection of Pax6 function: the specific roles of the paired domain and homeodomain in brain development , 2004, Development.

[74]  H. Peters,et al.  Molecular characterization of Pax6(2Neu) through Pax6(10Neu): an extension of the Pax6 allelic series and the identification of two possible hypomorph alleles in the mouse Mus musculus. , 2001, Genetics.

[75]  A. Meyer,et al.  Genome duplication, a trait shared by 22000 species of ray-finned fish. , 2003, Genome research.

[76]  E. Tamm,et al.  Genetic dissection of Pax6 dosage requirements in the developing mouse eye. , 2005, Human molecular genetics.

[77]  C. Nüsslein-Volhard,et al.  Genes involved in forebrain development in the zebrafish, Danio rerio. , 1996, Development.

[78]  A. Schedl,et al.  Aniridia-associated translocations, DNase hypersensitivity, sequence comparison and transgenic analysis redefine the functional domain of PAX6. , 2001, Human molecular genetics.

[79]  Nadav Ahituv,et al.  Exploiting human--fish genome comparisons for deciphering gene regulation. , 2004, Human molecular genetics.

[80]  S. Saule,et al.  Identification and Characterization of a Neuroretina-Specific Enhancer Element in the Quail Pax-6 ( Pax-QNR ) Gene , 2022 .

[81]  D. Duboule,et al.  HoxD cluster scanning deletions identify multiple defects leading to paralysis in the mouse mutant Ironside. , 2005, Genes & development.

[82]  H. Campbell,et al.  National study of microphthalmia, anophthalmia, and coloboma (MAC) in Scotland: investigation of genetic aetiology , 2002, Journal of medical genetics.

[83]  S. Fisher,et al.  Conservation of RET Regulatory Function from Human to Zebrafish Without Sequence Similarity , 2006, Science.

[84]  S. Brenner,et al.  Distinct cis-essential modules direct the time-space pattern of the Pax6 gene activity. , 1999, Developmental biology.

[85]  C. M. Stellrecht,et al.  Modulation of PAX6 Homeodomain Function by the Paired Domain* , 2000, The Journal of Biological Chemistry.

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

[87]  B. Oostra,et al.  A long-range Shh enhancer regulates expression in the developing limb and fin and is associated with preaxial polydactyly. , 2003, Human molecular genetics.

[88]  John Postlethwait,et al.  Subfunction partitioning, the teleost radiation and the annotation of the human genome. , 2004, Trends in genetics : TIG.

[89]  D. Landsman,et al.  Threading analysis of prospero-type homeodomains. , 1999, In silico biology.

[90]  C. Kimmel,et al.  Stages of embryonic development of the zebrafish , 1995, Developmental dynamics : an official publication of the American Association of Anatomists.

[91]  H. Baier,et al.  Loss of eyes in zebrafish caused by mutation of chokh/rx3 , 2003, EMBO reports.

[92]  Marie Sémon,et al.  Reciprocal gene loss between Tetraodon and zebrafish after whole genome duplication in their ancestor. , 2007, Trends in genetics : TIG.