2013 Biomedical Postdoc Research Symposium

The Biomedical Postdoctoral Council (BPC) and the Office of Biomedical Postdoctoral Programs (BPP) are pleased to announce:

The 12th Annual Biomedical Postdoctoral Research Symposium
November 4th, 2013
BRB II/III Auditorium and Lobby
421 Curie Boulevard, Philadelphia, PA 19104

The symposium will include:

This FREE event is a great way to practice your presentation skills and to learn about your fellow postdocs’ research. Posters have been very well-attended in past years, and the presenters pleased with the feedback they've received. All post-docs served by the Biomedical Postdoctoral Council (BPC) and Office of Biomedical Postdoctoral Programs (BPP) are welcome to present, and all members of the university community are welcome to attend.

I. Rules and Guidelines for abstract submission

Example abstract:

Genomics of systems neuroscience enabled: TIVA-tag mediated isolation of mRNA from single cells in their natural environment

Ditte Lovatt (1,2), Brittani Ruble (3), Jaehee Lee (1,2), Peter Buckley (1,2), Hannah Dueck (2,4), Julia Richards (3), Junhyong Kim (2,4), Jai-Yoon Sul (1,2), Ivan Dmochowski (2,3), and James Eberwine (1,2)

(1) Department of Pharmacology, Perelman School of Medicine, University of Pennsylvania; (2) PENN Genome Frontiers Institute, University of Pennsylvania; (3) Department of Chemistry, and (4) Department of Biology, School of Arts & Sciences, University of Pennsylvania

Transcriptome profiling is an indispensable tool in advancing biomedical research, but depends upon methods capable of isolating mRNA. While it is a trivial procedure to isolate mRNA from bulk tissue or cultures, isolation of mRNA from single cells in intact tissue remains a technical obstacle. This is due to the cellular complexity present in most tissues, and hence, the difficulty of dissecting single cells free of contamination from neighboring cellular parts. Consequently, single cell transcriptomics from complex tissues is largely unexplored. Here, we engineered a multifunctional chemical compound that we call Transcriptome In Vivo Analysis (TIVA) -tags, which allows mRNA isolation by imaging-assisted selective photoactivation of single cells in live tissue. TIVA-tags comprise an mRNA-binding property and can unidirectionally enter live cells in tissues. The mRNA-binding property of TIVA can be uncaged upon laser-derived photoactivation directed at a single cell. Following uncaging, the TIVA-tag anneals to mRNA inside the cell, and TIVA:mRNA hybrids can be isolated through affinity-purification. The purified mRNA can then be processed for transcriptome analysis. Using the TIVA approach to perform transcriptome analysis of single hippocampal neurons revealed enrichment of the neuronal markers Mtap2 and Snap25, but showed no enrichment of glial and vascular markers. These results confirmed the single cell specificity of the TIVA approach. TIVA-tags provide a novel approach to single cell mRNA isolation for RNA-seq transcriptome analysis, and enable the combination of single cell transcriptomics with other physiological, chemical and micro-environmental signatures of single cells.

II. Information for Poster Sessions

III. Information for Oral Sessions


IV. Awards

Prizes will be awarded for the best oral and poster presentations. Judges’ decisions are final and binding. Awards will be presented at the end of the symposium following the Keynote Lecture.

V. Contact

If you would like to volunteer for the 2013 committee, or if you have any questions regarding abstract submission, general participation or any other issues please contact Adam Walker, the Chair of the BPC Symposium Committee, at bpc.symposium@gmail.com, or the Office of Biomedical Postdoctoral Programs at postdoc@mail.med.upenn.edu or 215-573-4332.