Zebrafish mRNA sequencing deciphers novelties in transcriptome dynamics during maternal to zygotic transition

  1. Sinnakaruppan Mathavan2,10
  1. 1BasAM, Norwegian School of Veterinary Science, 0033 Oslo, Norway;
  2. 2Stem Cell and Developmental Biology, Genome Institute of Singapore, 138672 Singapore;
  3. 3Computational and Mathematical Biology, Genome Institute of Singapore, 138672 Singapore;
  4. 4Research Computing, Genome Institute of Singapore, 138672 Singapore;
  5. 5Institute of Basic Medical Sciences, Faculty of Medicine, University of Oslo, 0317 Oslo, Norway;
  6. 6Norwegian Center for Stem Cell Research, 0316 Oslo, Norway;
  7. 7Department of Biological Sciences, National University of Singapore, 117543 Singapore;
  8. 8Laboratory of Fish Developmental Biology, Institute of Molecular and Cell Biology, 138673 Singapore
    1. 9 These authors contributed equally to this work.

    Abstract

    Maternally deposited mRNAs direct early development before the initiation of zygotic transcription during mid-blastula transition (MBT). To study mechanisms regulating this developmental event in zebrafish, we applied mRNA deep sequencing technology and generated comprehensive information and valuable resources on transcriptome dynamics during early embryonic (egg to early gastrulation) stages. Genome-wide transcriptome analysis documented at least 8000 maternal genes and identified the earliest cohort of zygotic transcripts. We determined expression levels of maternal and zygotic transcripts with the highest resolution possible using mRNA-seq and clustered them based on their expression pattern. We unravel delayed polyadenylation in a large cohort of maternal transcripts prior to the MBT for the first time in zebrafish. Blocking polyadenylation of these transcripts confirms their role in regulating development from the MBT onward. Our study also identified a large number of novel transcribed regions in annotated and unannotated regions of the genome, which will facilitate reannotation of the zebrafish genome. We also identified splice variants with an estimated frequency of 50%–60%. Taken together, our data constitute a useful genomic information and valuable transcriptome resource for gene discovery and for understanding the mechanisms of early embryogenesis in zebrafish.

    Footnotes

    • 10 Corresponding author.

      E-mail mathavans{at}gis.a-star.edu.sg.

    • [Supplemental material is available for this article.]

    • Article published online before print. Article, supplemental material, and publication date are at http://www.genome.org/cgi/doi/10.1101/gr.116012.110.

    • Received September 30, 2010.
    • Accepted April 19, 2011.

    Freely available online through the Genome Research Open Access option.

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