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Sci Rep
2019 Dec 20;91:19559. doi: 10.1038/s41598-019-56085-8.
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Lampreys, the jawless vertebrates, contain three Pax6 genes with distinct expression in eye, brain and pancreas.
Ravi V
,
Bhatia S
,
Shingate P
,
Tay BH
,
Venkatesh B
,
Kleinjan DA
.
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The transcription factor Pax6 is crucial for the development of the central nervous system, eye, olfactory system and pancreas, and is implicated in human disease. While a single Pax6 gene exists in human and chicken, Pax6 occurs as a gene family in other vertebrates, with two members in elephant shark, Xenopus tropicalis and Anolis lizard and three members in teleost fish such as stickleback and medaka. However, the complement of Pax6 genes in jawless vertebrates (cyclostomes), the sister group of jawed vertebrates (gnathostomes), is unknown. Using a combination of BAC sequencing and genome analysis, we discovered three Pax6 genes in lampreys. Unlike the paired-less Pax6 present in some gnathostomes, all three lamprey Pax6 have a highly conserved full-length paired domain. All three Pax6 genes are expressed in the eye and brain, with variable expression in other tissues. Notably, lamprey Pax6α transcripts are found in the pancreas, a vertebrate-specific organ, indicating the involvement of Pax6 in development of the pancreas in the vertebrate ancestor. Multi-species sequence comparisons revealed only a single conserved non-coding element, in the lamprey Pax6β locus, with similarity to the PAX6 neuroretina enhancer. Using a transgenic zebrafish enhancer assay we demonstrate functional conservation of this element over 500 million years of vertebrate evolution.
Figure 1. The lamprey genome contains three Pax6 genes. (a) The three Pax6 loci in the Japanese lamprey, L. japonicum. Lamprey Pax6 genes are named Pax6α, Pax6β and Pax6γ. The BAC clones sequenced are shown below. LjPax6γ resides on a short (66âkb) scaffold containing no other genes. (b) Gene synteny comparison of the three Japanese lamprey (Jlamprey) and sea lamprey Pax6 loci with Pax6 loci from selected gnathostomes.
Figure 2. Protein sequences and expression patterns of the Japanese lamprey Pax6 genes. (a) Comparison of the amino acid sequences of LjPax6α, LjPax6β and LjPax6γ with human (Hs) PAX6. All three LjPax6 genes encode a highly conserved paired domain (solid black line), in contrast to known Pax6.2 (also referred to as Pax1014) genes which lack the sequences coding for this domain, as well as a highly conserved homeodomain (dotted grey line) and C-terminal transactivation domain. No evidence was found for the presence of the alternative exon 5a in the lamprey genes. The positions of the exon boundaries (black arrow head, phase 0 intron; open arrow head, phase 1 intron) are conserved between the human and lamprey genes. (b) qRT-PCR analysis using a panel of adult lamprey tissues showing the tissue-specific expression pattern of the LjPax6 genes. All three genes are highly expressed in the eye and brain, with lower and variable expression in other tissues.
Figure 3. Maximum Likelihood tree of vertebrate Pax6 genes. Phylogenetic analysis of the lamprey Pax6 genes with Pax6, Pax4, Pax3 and Pax7 genes from several other chordate species. The Pax3/7 clade was specified as the outgroup. The phylogram is shown on the left and its cladogram on the right. The tree highlights clustering of the three lamprey genes with Pax6 genes from other chordates thereby indicating that they are indeed lamprey Pax6 genes.
Figure 4. An ancient vertebrate conserved non-coding element is present in the lamprey Pax6β locus. (a) VISTA plot of the SLAGAN alignment of the LjPax6β locus, against the two Pax6 loci from elephant shark and human, as well as the amphioxus locus. Note that there is no PAX6 gene in the virtual âhuman_6.2â locus. Sequence similarity outside of exons was seen for only a single element, homologous to the PAX6 neuroretina enhancer (NRE). (b) Conservation at the core sequence of the NRE element. (c) Transgenic zebrafish assay of the LjPax6β putative NRE element. The Lj_NRE element was cloned in front of a minimal promoter-eGFP cassette and used to generate stable transgenic fish. Embryos at 24, 36, 48 and 72âhours post fertilisation (hpf) show highly specific and consistent GFP signal in the neuroretina of the developing eye. Ectopic expression in the heart due to site of integration effect was seen in one of the transgenic lines. Embryos were imaged from the lateral side (24 hpf and inset 72 hpf showing a close-up of the eye) or ventral side (36 hpf, 48 hpf and 72 hpf) with the fluorescent confocal signal overlaid on a brightfield view. L, lens; NR, neuroretina; h, heart.
Antosova,
The Gene Regulatory Network of Lens Induction Is Wired through Meis-Dependent Shadow Enhancers of Pax6.
2016, Pubmed
Antosova,
The Gene Regulatory Network of Lens Induction Is Wired through Meis-Dependent Shadow Enhancers of Pax6.
2016,
Pubmed
Ashery-Padan,
Pax6 activity in the lens primordium is required for lens formation and for correct placement of a single retina in the eye.
2000,
Pubmed
Bhatia,
Functional assessment of disease-associated regulatory variants in vivo using a versatile dual colour transgenesis strategy in zebrafish.
2015,
Pubmed
Bhatia,
A survey of ancient conserved non-coding elements in the PAX6 locus reveals a landscape of interdigitated cis-regulatory archipelagos.
2014,
Pubmed
,
Xenbase
Brudno,
Glocal alignment: finding rearrangements during alignment.
2003,
Pubmed
Coffill,
The p53-Mdm2 interaction and the E3 ligase activity of Mdm2/Mdm4 are conserved from lampreys to humans.
2016,
Pubmed
Cvekl,
PAX6: 25th anniversary and more to learn.
2017,
Pubmed
Dehal,
Two rounds of whole genome duplication in the ancestral vertebrate.
2005,
Pubmed
Derobert,
Pax6 expression patterns in Lampetra fluviatilis and Scyliorhinus canicula embryos suggest highly conserved roles in the early regionalization of the vertebrate brain.
,
Pubmed
Dimanlig,
The upstream ectoderm enhancer in Pax6 has an important role in lens induction.
2001,
Pubmed
Dohrmann,
Pax genes and the differentiation of hormone-producing endocrine cells in the pancreas.
2000,
Pubmed
Epstein,
Two independent and interactive DNA-binding subdomains of the Pax6 paired domain are regulated by alternative splicing.
1994,
Pubmed
Ewing,
Base-calling of automated sequencer traces using phred. I. Accuracy assessment.
1998,
Pubmed
Fabian,
Pax2/5/8 and Pax6 alternative splicing events in basal chordates and vertebrates: a focus on paired box domain.
2015,
Pubmed
Feiner,
Evolution of the vertebrate Pax4/6 class of genes with focus on its novel member, the Pax10 gene.
2014,
Pubmed
,
Xenbase
Fisher,
Evaluating the biological relevance of putative enhancers using Tol2 transposon-mediated transgenesis in zebrafish.
2006,
Pubmed
Gordon,
Consed: a graphical tool for sequence finishing.
1998,
Pubmed
Gosmain,
Pax6 is crucial for β-cell function, insulin biosynthesis, and glucose-induced insulin secretion.
2012,
Pubmed
Hart,
The developmental regulator Pax6 is essential for maintenance of islet cell function in the adult mouse pancreas.
2013,
Pubmed
Hastie,
Wilms' tumour 1 (WT1) in development, homeostasis and disease.
2017,
Pubmed
Hill,
Mouse small eye results from mutations in a paired-like homeobox-containing gene.
,
Pubmed
Kammandel,
Distinct cis-essential modules direct the time-space pattern of the Pax6 gene activity.
1999,
Pubmed
Kim,
The LIM protein complex establishes a retinal circuitry of visual adaptation by regulating Pax6 α-enhancer activity.
2017,
Pubmed
Kleinjan,
Aniridia-associated translocations, DNase hypersensitivity, sequence comparison and transgenic analysis redefine the functional domain of PAX6.
2001,
Pubmed
Klimova,
Stage-dependent requirement of neuroretinal Pax6 for lens and retina development.
2014,
Pubmed
Kohany,
Annotation, submission and screening of repetitive elements in Repbase: RepbaseSubmitter and Censor.
2006,
Pubmed
Kozmik,
Alternatively spliced insertions in the paired domain restrict the DNA sequence specificity of Pax6 and Pax8.
1997,
Pubmed
Kuraku,
Time scale for cyclostome evolution inferred with a phylogenetic diagnosis of hagfish and lamprey cDNA sequences.
2006,
Pubmed
Lamb,
Evolution of the vertebrate eye: opsins, photoreceptors, retina and eye cup.
2007,
Pubmed
Livak,
Analysis of relative gene expression data using real-time quantitative PCR and the 2(-Delta Delta C(T)) Method.
2001,
Pubmed
Marlétaz,
Amphioxus functional genomics and the origins of vertebrate gene regulation.
2018,
Pubmed
Marquardt,
Pax6 is required for the multipotent state of retinal progenitor cells.
2001,
Pubmed
Mayor,
VISTA : visualizing global DNA sequence alignments of arbitrary length.
2000,
Pubmed
McBride,
DNaseI hypersensitivity and ultraconservation reveal novel, interdependent long-range enhancers at the complex Pax6 cis-regulatory region.
2011,
Pubmed
McEwen,
Early evolution of conserved regulatory sequences associated with development in vertebrates.
2009,
Pubmed
Mehta,
Evidence for at least six Hox clusters in the Japanese lamprey (Lethenteron japonicum).
2013,
Pubmed
Miyashita,
Hagfish from the Cretaceous Tethys Sea and a reconciliation of the morphological-molecular conflict in early vertebrate phylogeny.
2019,
Pubmed
Mulley,
Transcriptomic analysis of the lesser spotted catshark (Scyliorhinus canicula) pancreas, liver and brain reveals molecular level conservation of vertebrate pancreas function.
2014,
Pubmed
Murakami,
Identification and expression of the lamprey Pax6 gene: evolutionary origin of the segmented brain of vertebrates.
2001,
Pubmed
Nah,
Characterization of the Runx gene family in a jawless vertebrate, the Japanese lamprey (Lethenteron japonicum).
2014,
Pubmed
Nakayama,
Xenopus pax6 mutants affect eye development and other organ systems, and have phenotypic similarities to human aniridia patients.
2015,
Pubmed
,
Xenbase
Oron-Karni,
Dual requirement for Pax6 in retinal progenitor cells.
2008,
Pubmed
Osumi,
Concise review: Pax6 transcription factor contributes to both embryonic and adult neurogenesis as a multifunctional regulator.
2008,
Pubmed
Plaza,
Identification and characterization of a neuroretina-specific enhancer element in the quail Pax-6 (Pax-QNR) gene.
1995,
Pubmed
Putnam,
The amphioxus genome and the evolution of the chordate karyotype.
2008,
Pubmed
Qiu,
Unresolved orthology and peculiar coding sequence properties of lamprey genes: the KCNA gene family as test case.
2011,
Pubmed
Ravi,
Sequencing of Pax6 loci from the elephant shark reveals a family of Pax6 genes in vertebrate genomes, forged by ancient duplications and divergences.
2013,
Pubmed
Remez,
Pax6 is essential for the generation of late-born retinal neurons and for inhibition of photoreceptor-fate during late stages of retinogenesis.
2017,
Pubmed
Schmidt,
TREE-PUZZLE: maximum likelihood phylogenetic analysis using quartets and parallel computing.
2002,
Pubmed
Simpson,
Pax6; a pleiotropic player in development.
2002,
Pubmed
Smith,
The sea lamprey germline genome provides insights into programmed genome rearrangement and vertebrate evolution.
2018,
Pubmed
Smith,
The sea lamprey meiotic map improves resolution of ancient vertebrate genome duplications.
2015,
Pubmed
St-Onge,
Pax6 is required for differentiation of glucagon-producing alpha-cells in mouse pancreas.
1997,
Pubmed
Xu,
Regulation of Pax6 expression is conserved between mice and flies.
1999,
Pubmed
Youson,
Ontogenetic and phylogenetic development of the endocrine pancreas (islet organ) in fish.
1999,
Pubmed
Yue,
Conserved Noncoding Elements in the Most Distant Genera of Cephalochordates: The Goldilocks Principle.
2016,
Pubmed
Zhang,
Lampreys, the jawless vertebrates, contain only two ParaHox gene clusters.
2017,
Pubmed