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Analysis of embryonic development in the unsequenced axolotl: Waves of transcriptomic upheaval and stability.
Jiang, Peng; Nelson, Jeffrey D; Leng, Ning; Collins, Michael; Swanson, Scott; Dewey, Colin N; Thomson, James A; Stewart, Ron.
Affiliation
  • Jiang P; Regenerative Biology, Morgridge Institute for Research, Madison, WI, United States.
  • Nelson JD; Regenerative Biology, Morgridge Institute for Research, Madison, WI, United States.
  • Leng N; Regenerative Biology, Morgridge Institute for Research, Madison, WI, United States.
  • Collins M; Regenerative Biology, Morgridge Institute for Research, Madison, WI, United States.
  • Swanson S; Regenerative Biology, Morgridge Institute for Research, Madison, WI, United States.
  • Dewey CN; Department of Biostatistics and Medical Informatics, University of Wisconsin, Madison, WI, United States.
  • Thomson JA; Regenerative Biology, Morgridge Institute for Research, Madison, WI, United States; Department of Cell and Regenerative Biology, University of Wisconsin, Madison, WI, United States; Department of Molecular, Cellular, and Developmental Biology, University of California, Santa Barbara, CA, United Stat
  • Stewart R; Regenerative Biology, Morgridge Institute for Research, Madison, WI, United States. Electronic address: rstewart@morgridge.org.
Dev Biol ; 426(2): 143-154, 2017 06 15.
Article in En | MEDLINE | ID: mdl-27475628
The axolotl (Ambystoma mexicanum) has long been the subject of biological research, primarily owing to its outstanding regenerative capabilities. However, the gene expression programs governing its embryonic development are particularly underexplored, especially when compared to other amphibian model species. Therefore, we performed whole transcriptome polyA+ RNA sequencing experiments on 17 stages of embryonic development. As the axolotl genome is unsequenced and its gene annotation is incomplete, we built de novo transcriptome assemblies for each stage and garnered functional annotation by comparing expressed contigs with known genes in other organisms. In evaluating the number of differentially expressed genes over time, we identify three waves of substantial transcriptome upheaval each followed by a period of relative transcriptome stability. The first wave of upheaval is between the one and two cell stage. We show that the number of differentially expressed genes per unit time is higher between the one and two cell stage than it is across the mid-blastula transition (MBT), the period of zygotic genome activation. We use total RNA sequencing to demonstrate that the vast majority of genes with increasing polyA+ signal between the one and two cell stage result from polyadenylation rather than de novo transcription. The first stable phase begins after the two cell stage and continues until the mid-blastula transition, corresponding with the pre-MBT phase of transcriptional quiescence in amphibian development. Following this is a peak of differential gene expression corresponding with the activation of the zygotic genome and a phase of transcriptomic stability from stages 9-11. We observe a third wave of transcriptomic change between stages 11 and 14, followed by a final stable period. The last two stable phases have not been documented in amphibians previously and correspond to times of major morphogenic change in the axolotl embryo: gastrulation and neurulation. These results yield new insights into global gene expression during early stages of amphibian embryogenesis and will help to further develop the axolotl as a model species for developmental and regenerative biology.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Gene Expression Regulation, Developmental / Embryonic Development / Transcriptome / Ambystoma mexicanum Limits: Animals Language: En Journal: Dev Biol Year: 2017 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Gene Expression Regulation, Developmental / Embryonic Development / Transcriptome / Ambystoma mexicanum Limits: Animals Language: En Journal: Dev Biol Year: 2017 Document type: Article