Deep Sequencing Study Reveals New Insights into Human Transcriptome

They found that 34% of the polyadenylated transcriptome mapped to so far non-annotated genomic regions. Obviously, a large number of novel gene candidates are active in the cell lines under examination. In addition, a global survey of mRNA splicing events identified 94,241 splice junctions, of which 4,096 are novel, and showed that exon skipping is the most prevalent form of alternative splicing.

Details were published by Dr. P. K. Sultan and colleagues online in July 2008, at Science Express.

Dr. Marie-Laure Yaspo, group leader at the MPI MolGen and head scientist of the study stated, "Deep sequencing allows for the first time to explore directly the complexity and dynamics of the human transcriptome with a reasonable effort. This will lead to a new picture of the mammalian genome annotation far beyond the current state of the art. We provide here global features of alternative splicing events in human cell lines. Such a comparison of within-cell and between-cell alternative splicing events, combined with the simultaneous analysis of gene expression has never been presented before. It becomes clear that the so far available methods only delivered a part of the transcriptional landscape of mammalian cells, especially if gene regulation analysis is considered.”

Dr. Martin Seifert, vice president business development and consulting at Genomatix stated, "The main biological impact is the observation of a new dimension in complexity and variability. Based on the method we could find a significant number of new transcriptional units and splice variants. Our analyses clearly show that transcription is a highly dynamic and variable process. We learned a lot by having access to such high quality data and co-developed necessary new analysis strategies with the MPI MolGen. Especially users of our brand new Genomatix genome analyzer will benefit from our experiences along the project, since they have access to all developed strategies.”


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