Microarray and cDNA sequence analysis of transcription during nerve-dependent limb regeneration

BackgroundMicroarray analysis and 454 cDNA sequencing were used to investigate a centuries-old problem in regenerative biology: the basis of nerve-dependent limb regeneration in salamanders. Innervated (NR) and denervated (DL) forelimbs of Mexican axolotls were amputated and transcripts were sampled after 0, 5, and 14 days of regeneration.ResultsConsiderable similarity was observed between NR and DL transcriptional programs at 5 and 14 days post amputation (dpa). Genes with extracellular functions that are critical to wound healing were upregulated while muscle-specific genes were downregulated. Thus, many processes that are regulated during early limb regeneration do not depend upon nerve-derived factors. The majority of the transcriptional differences between NR and DL limbs were correlated with blastema formation; cell numbers increased in NR limbs after 5 dpa and this yielded distinct transcriptional signatures of cell proliferation in NR limbs at 14 dpa. These transcriptional signatures were not observed in DL limbs. Instead, gene expression changes within DL limbs suggest more diverse and protracted wound-healing responses. 454 cDNA sequencing complemented the microarray analysis by providing deeper sampling of transcriptional programs and associated biological processes. Assembly of new 454 cDNA sequences with existing expressed sequence tag (EST) contigs from the Ambystoma EST database more than doubled (3935 to 9411) the number of non-redundant human-A. mexicanum orthologous sequences.ConclusionMany new candidate gene sequences were discovered for the first time and these will greatly enable future studies of wound healing, epigenetics, genome stability, and nerve-dependent blastema formation and outgrowth using the axolotl model.

[1]  T. G. Connelly,et al.  A staging system for forelimb regeneration in the axolotl, Ambystoma mexicanum , 1976, Journal of morphology.

[2]  G. Zupi,et al.  CCCTC-binding Factor Activates PARP-1 Affecting DNA Methylation Machinery , 2008, Journal of Biological Chemistry.

[3]  Stéphane Roy,et al.  Transforming Growth Factor: β Signaling Is Essential for Limb Regeneration in Axolotls , 2007, PloS one.

[4]  M. Singer On the Nature of the Neurotrophic Phenomenon in Urodele Limb Regeneration , 1978 .

[5]  Frédérick A. Mallette,et al.  Urodele p53 tolerates amino acid changes found in p53 variants linked to human cancer , 2007, BMC Evolutionary Biology.

[6]  S. Bryant,et al.  Nerve dependency of regeneration: the role of Distal-less and FGF signaling in amphibian limb regeneration. , 1996, Development.

[7]  S. Voss,et al.  Transcriptional response of Mexican axolotls to Ambystoma tigrinum virus (ATV) infection , 2008, BMC Genomics.

[8]  J. Deck The histological effects of partial denervation and amputation in larval salamander forelimbs. , 1961, The Journal of experimental zoology.

[9]  J. Marden,et al.  Rapid transcriptome characterization for a nonmodel organism using 454 pyrosequencing , 2008, Molecular ecology.

[10]  S. Voss,et al.  Microarray analysis identifies keratin loci as sensitive biomarkers for thyroid hormone disruption in the salamander Ambystoma mexicanum. , 2007, Comparative biochemistry and physiology. Toxicology & pharmacology : CBP.

[11]  J. O. Thomas,et al.  HMG1 and 2: architectural DNA-binding proteins. , 2001, Biochemical Society transactions.

[12]  H. Sasaki,et al.  Correlation between Shh expression and DNA methylation status of the limb-specific Shh enhancer region during limb regeneration in amphibians. , 2007, Developmental biology.

[13]  Deck Jd The histological effects of partial denervation and amputation in larval salamander forelimbs. , 1961 .

[14]  John Quackenbush,et al.  Genesis: cluster analysis of microarray data , 2002, Bioinform..

[15]  M. Dresden,et al.  Denervation effects on newt limb regeneration: DNA, RNA, and protein synthesis. , 1969, Developmental biology.

[16]  S. Kulkarni,et al.  Flap Endonuclease 1 Contributes to Telomere Stability , 2008, Current Biology.

[17]  S. Bryant,et al.  Vertebrate limb regeneration and the origin of limb stem cells. , 2002, The International journal of developmental biology.

[18]  J. Brockes,et al.  Plasticity of retrovirus-labelled myotubes in the newt limb regeneration blastema. , 2000, Developmental biology.

[19]  K. Mitsuya,et al.  The SRA protein Np95 mediates epigenetic inheritance by recruiting Dnmt1 to methylated DNA , 2007, Nature.

[20]  E. Hay Electron microscopic observations of muscle dedifferentiation in regenerating amblystoma limbs , 1959 .

[21]  M. Singer,et al.  Nerve dependent macromolecular synthesis in the epidermis and blastema of the adult newt regenerate. , 1978, The Journal of experimental zoology.

[22]  Anoop Kumar,et al.  The Regenerative Plasticity of Isolated Urodele Myofibers and Its Dependence on Msx1 , 2004, PLoS biology.

[23]  Rafael A. Irizarry,et al.  Bioinformatics and Computational Biology Solutions using R and Bioconductor , 2005 .

[24]  Benjamin M. Bolstad,et al.  Preprocessing High-density Oligonucleotide Arrays , 2005 .

[25]  K. Mulder,et al.  Human Ccr4‐Not complex is a ligand‐dependent repressor of nuclear receptor‐mediated transcription , 2006, The EMBO journal.

[26]  M. Singer,et al.  The Influence of the Nerve in Regeneration of the Amphibian Extremity , 1952, The Quarterly Review of Biology.

[27]  Steven C. Lawlor,et al.  GenMAPP, a new tool for viewing and analyzing microarray data on biological pathways , 2002, Nature Genetics.

[28]  R. Tassava,et al.  Cellular events in denervated limb stumps ofAmbystoma larvae during re-innervation and subsequent regeneration , 1980, Experientia.

[29]  A. Mescher,et al.  Transferrin is necessary and sufficient for the neural effect on growth in amphibian limb regeneration blastemas , 1997, Development, growth & differentiation.

[30]  M. Singer,et al.  Scanning electron microscopy of the normal and denervated limb regenerate in the newt, Notophthalmus, including observations on embryonic amphibia limb-bud mesenchyme and blastemas of fish-fin regenerates. , 1981, The American journal of anatomy.

[31]  M. Maden Neurotrophic control of the cell cycle during amphibian limb regeneration. , 1978, Journal of embryology and experimental morphology.

[32]  E. Schnapp,et al.  Quantitative evaluation of morpholino‐mediated protein knockdown of GFP, MSX1, and PAX7 during tail regeneration in Ambystoma mexicanum , 2005, Developmental dynamics : an official publication of the American Association of Anatomists.

[33]  A. Mescher The cellular basis of limb regeneration in urodeles. , 1996, The International journal of developmental biology.

[34]  J. Utikal,et al.  Directly reprogrammed fibroblasts show global epigenetic remodeling and widespread tissue contribution. , 2007, Cell stem cell.

[35]  E. Tanaka,et al.  Hedgehog signaling controls dorsoventral patterning, blastema cell proliferation and cartilage induction during axolotl tail regeneration , 2005, Development.

[36]  J. Brockes,et al.  Cell origin and identity in Limb regeneration and development , 1991, Glia.

[37]  M. Mateyak,et al.  Human PIF Helicase is Cell Cycle Regulated and Associates with Telomerase , 2006, Cell cycle.

[38]  L. Bennett,et al.  DNA synthesis without mitosis in amputated denervated forelimbs of larval axolotls. , 1974, The Journal of experimental zoology.

[39]  J. Richardson,et al.  Transcriptional profiling and regulation of the extracellular matrix during muscle regeneration. , 2003, Physiological genomics.

[40]  K. Tamura,et al.  FGF-10 stimulates limb regeneration ability in Xenopus laevis. , 2001, Developmental biology.

[41]  R. Tassava,et al.  Responses to amputation of denervated ambystoma limbs containing aneurogenic limb grafts. , 2003, Journal of experimental zoology. Part A, Comparative experimental biology.

[42]  P. Sassone-Corsi,et al.  Inhibition of Aurora-B kinase activity by poly(ADP-ribosyl)ation in response to DNA damage. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[43]  R. Tassava,et al.  Rescue of blocked cells by reinnervation in denervated forelimb stumps of larval Ambystoma. , 1984, Developmental biology.

[44]  P. B. Gates,et al.  The newt ortholog of CD59 is implicated in proximodistal identity during amphibian limb regeneration. , 2002, Developmental cell.

[45]  M. Marchionni,et al.  Cloning and neuronal expression of a type III newt neuregulin and rescue of denervated, nerve-dependent newt limb blastemas by rhGGF2. , 2000, Journal of neurobiology.

[46]  M. Weinstein,et al.  Fibroblast growth factors in regenerating limbs of Ambystoma: cloning and semi-quantitative RT-PCR expression studies. , 2001, The Journal of experimental zoology.

[47]  Brad T. Sherman,et al.  DAVID: Database for Annotation, Visualization, and Integrated Discovery , 2003, Genome Biology.

[48]  P. L. Puri,et al.  The epigenetic network regulating muscle development and regeneration , 2006, Journal of cellular physiology.

[49]  W Brad Barbazuk,et al.  Gene discovery and annotation using LCM-454 transcriptome sequencing. , 2006, Genome research.

[50]  David I. K. Martin,et al.  Controlling elements are wild cards in the epigenomic deck , 2007, Proceedings of the National Academy of Sciences.

[51]  X. Huang,et al.  CAP3: A DNA sequence assembly program. , 1999, Genome research.

[52]  E. G. Butler,et al.  Morphological effects of denervation and amputation of limbs in urodele larvae , 1941 .

[53]  Rafael A Irizarry,et al.  Exploration, normalization, and summaries of high density oligonucleotide array probe level data. , 2003, Biostatistics.

[54]  T. G. Connelly,et al.  Microdensitometric analysis of denervation effects on newt limb blastema cells , 2005, Experientia.

[55]  Gordon K. Smyth,et al.  Use of within-array replicate spots for assessing differential expression in microarray experiments , 2005, Bioinform..

[56]  A. Satoh,et al.  Nerve-dependent and -independent events in blastema formation during Xenopus froglet limb regeneration. , 2005, Developmental biology.

[57]  E. Buratti,et al.  Multiple roles of TDP-43 in gene expression, splicing regulation, and human disease. , 2008, Frontiers in bioscience : a journal and virtual library.

[58]  M. Singer,et al.  Neurotrophic dependence of macromolecular synthesis in the early limb regenerate of the newt, Triturus. , 1972, Journal of embryology and experimental morphology.

[59]  T. Fujioka,et al.  Rho/Rho-associated Kinase Signal Regulates Myogenic Differentiation via Myocardin-related Transcription Factor-A/Smad-dependent Transcription of the Id3 Gene* , 2008, Journal of Biological Chemistry.

[60]  A. Mescher,et al.  Denervation effects on DNA replication and mitosis during the initiation of limb regeneration in adult newts. , 1975, Developmental biology.

[61]  S. Bryant,et al.  Nerve-induced ectopic limb blastemas in the Axolotl are equivalent to amputation-induced blastemas. , 2007, Developmental biology.

[62]  Srinivas Aluru,et al.  Efficient clustering of large EST data sets on parallel computers. , 2003, Nucleic acids research.

[63]  Terence P. Speed,et al.  Quality Assessment of Affymetrix GeneChip Data , 2005 .

[64]  Michael John Smith,et al.  Evidence Supporting a Mitogenic Role for Substance P in Amphibian Limb Regeneration , 1991, Annals of the New York Academy of Sciences.

[65]  J. Nickoloff,et al.  Regulation of DNA double-strand break repair pathway choice , 2008, Cell Research.

[66]  J. An,et al.  Expression patterns of Fgf‐8 during development and limb regeneration of the axolotl , 2001, Developmental dynamics : an official publication of the American Association of Anatomists.

[67]  S. Voss,et al.  Early gene expression during natural spinal cord regeneration in the salamander Ambystoma mexicanum , 2006, Journal of neurochemistry.

[68]  C. S. Thornton Histological modifications in denervated injured fore limbs of Amblystoma larvae , 1953 .

[69]  Gordon K Smyth,et al.  Statistical Applications in Genetics and Molecular Biology Linear Models and Empirical Bayes Methods for Assessing Differential Expression in Microarray Experiments , 2011 .

[70]  N. Mercader,et al.  Proximodistal identity during vertebrate limb regeneration is regulated by Meis homeodomain proteins , 2005, Development.

[71]  Hua Yang,et al.  Aurora-A Kinase Regulates Telomerase Activity through c-Myc in Human Ovarian and Breast Epithelial Cells , 2004, Cancer Research.

[72]  Z. Szallasi,et al.  Reliability and reproducibility issues in DNA microarray measurements. , 2006, Trends in genetics : TIG.

[73]  S. Voss,et al.  Effect of thyroid hormone concentration on the transcriptional response underlying induced metamorphosis in the Mexican axolotl (Ambystoma) , 2008, BMC Genomics.

[74]  M. Singer,et al.  Neurotrophic Control of Protein Synthesis in the Regenerating Limb of the Newt, Triturus , 1970, Nature.

[75]  R. Tassava,et al.  Cell cycle and histological effects of reinnervation in denervated forelimb stumps of larval Ambystoma. , 1984, The Journal of experimental zoology.

[76]  M. Durán,et al.  L-serine in disease and development. , 2003, The Biochemical journal.

[77]  A. Bürkle,et al.  Poly(ADP-ribosyl)ation in mammalian ageing , 2007, Nucleic acids research.

[78]  M. Globus,et al.  Nerve extracts and substance P activate the phosphatidylinositol signaling pathway and mitogenesis in newt forelimb regenerates. , 1995, Developmental biology.

[79]  S. Bryant,et al.  The effects of denervation on the ultrastructure of young limb regenerates in the newt, Triturus. , 1971, Developmental biology.

[80]  J. Clarke,et al.  In vivo imaging indicates muscle fiber dedifferentiation is a major contributor to the regenerating tail blastema. , 2001, Developmental biology.

[81]  J. Brockes,et al.  Glial growth factor and nerve-dependent proliferation in the regeneration blastema of urodele amphibians , 1986, Cell.

[82]  R. Sicard Regulation of vertebrate limb regeneration , 1985 .

[83]  S. Bryant,et al.  Analysis of the expression and function of Wnt‐5a and Wnt‐5b in developing and regenerating axolotl (Ambystoma mexicanum) limbs , 2008, Development, growth & differentiation.

[84]  H. Kurahashi,et al.  Genetically regulated epigenetic transcriptional activation of retrotransposon insertion confers mouse dactylaplasia phenotype , 2007, Proceedings of the National Academy of Sciences.

[85]  Matthew E Hudson,et al.  Wasp Gene Expression Supports an Evolutionary Link Between Maternal Behavior and Eusociality , 2007, Science.

[86]  P. Tank,et al.  The distribution of cells in the upper forelimb of the axolotl, Ambystoma mexicanum , 1979 .

[87]  M. Weinstein,et al.  Expression of fibroblast growth factors 4, 8, and 10 in limbs, flanks, and blastemas of Ambystoma , 2002, Developmental dynamics : an official publication of the American Association of Anatomists.

[88]  S. Bryant,et al.  Neurotrophic regulation of epidermal dedifferentiation during wound healing and limb regeneration in the axolotl (Ambystoma mexicanum). , 2008, Developmental biology.

[89]  E. G. Butler,et al.  Histological alterations in denervated non-regenerating limbs of urodele larvae , 1941 .

[90]  B. C. Irvin,et al.  Effects of peripheral nerve implants on the regeneration of partially and fully innervated urodele forelimbs , 1998, Wound repair and regeneration : official publication of the Wound Healing Society [and] the European Tissue Repair Society.

[91]  Anoop Kumar,et al.  Molecular Basis for the Nerve Dependence of Limb Regeneration in an Adult Vertebrate , 2007, Science.

[92]  J. Davis Bioinformatics and Computational Biology Solutions Using R and Bioconductor , 2007 .

[93]  R. Foisner,et al.  Nucleoplasmic lamins and their interaction partners, LAP2α, Rb, and BAF, in transcriptional regulation , 2007, The FEBS journal.

[94]  András Simon,et al.  Salamander limb regeneration involves the activation of a multipotent skeletal muscle satellite cell population , 2006, The Journal of cell biology.

[95]  J. Brockes,et al.  Reversal of muscle differentiation during urodele limb regeneration. , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[96]  John W M Martens,et al.  Association of DNA methylation of phosphoserine aminotransferase with response to endocrine therapy in patients with recurrent breast cancer. , 2005, Cancer research.

[97]  S. Bryant,et al.  Expression of Hoxb13 and Hoxc10 in developing and regenerating Axolotl limbs and tails. , 2001, Developmental biology.

[98]  Bianca Habermann,et al.  From biomedicine to natural history research: EST resources for ambystomatid salamanders , 2004, BMC Genomics.

[99]  S. Bryant,et al.  A stepwise model system for limb regeneration. , 2004, Developmental biology.

[100]  Allen R. Hilgers,et al.  Evidence that reserve cells are a source of regenerated adult newt muscle in vitro , 1986, Nature.

[101]  R. Tassava,et al.  Kinetics of cell cycle entry in innervated and denervated forelimb stumps of larval Ambystoma , 1985 .

[102]  S. Voss,et al.  Isolation and characterization of axolotl NPDC-1 and its effects on retinoic acid receptor signaling. , 2007, Comparative biochemistry and physiology. Part B, Biochemistry & molecular biology.

[103]  V. Denis,et al.  Overexpression of phosphoserine aminotransferase PSAT1 stimulates cell growth and increases chemoresistance of colon cancer cells , 2008, Molecular Cancer.

[104]  S. Costa,et al.  'Open minded' cells: how cells can change fate. , 2007, Trends in cell biology.