A Tissue-Mapped Axolotl De Novo Transcriptome Enables Identification of Limb Regeneration Factors

Donald M. Bryant(Harvard Stem Cell Institute), K.A. Johnson(Harvard Stem Cell Institute), Tia DiTommaso(Brigham and Women's Hospital), Timothy L. Tickle(Broad Institute), Matthew Brian Couger(Oklahoma State University), Duygu Payzin‐Dogru(Brigham and Women's Hospital), Tae J. Lee(Brigham and Women's Hospital), Nicholas D. Leigh(Brigham and Women's Hospital), Tzu‐Hsing Kuo(Harvard Stem Cell Institute), Francis G. Davis(Brigham and Women's Hospital), Joel Bateman(Harvard University), Sevara Bryant(Brigham and Women's Hospital), Anna R. Guzikowski(Harvard University), Stephanie Tsai(Harvard University), Steven Coyne(Harvard University), William W. Ye(Brigham and Women's Hospital), Robert M. Freeman(Center for Systems Biology), Leonid Peshkin(Center for Systems Biology), Clifford J. Tabin(Harvard University), Aviv Regev(Broad Institute), Brian J. Haas(Broad Institute), Jessica L. Whited(Brigham and Women's Hospital)
Cell Reports
January 1, 2017
Cited by 1,087Open Access
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Abstract

Mammals have extremely limited regenerative capabilities; however, axolotls are profoundly regenerative and can replace entire limbs. The mechanisms underlying limb regeneration remain poorly understood, partly because the enormous and incompletely sequenced genomes of axolotls have hindered the study of genes facilitating regeneration. We assembled and annotated a de novo transcriptome using RNA-sequencing profiles for a broad spectrum of tissues that is estimated to have near-complete sequence information for 88% of axolotl genes. We devised expression analyses that identified the axolotl orthologs of cirbp and kazald1 as highly expressed and enriched in blastemas. Using morpholino anti-sense oligonucleotides, we find evidence that cirbp plays a cytoprotective role during limb regeneration whereas manipulation of kazald1 expression disrupts regeneration. Our transcriptome and annotation resources greatly complement previous transcriptomic studies and will be a valuable resource for future research in regenerative biology.


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