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Monday, March 10, 2008
8:00 – 9:00 Registration for Pre-Conference Workshop
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9:00- 12:00 Pre-Conference Workshop |
Sponsored
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| Separate Registration
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TOOLS AND TECHNOLOGIES
FOR
microRNA ANALYSIS
9:00 am Welcoming Remarks from Conference Director
9:05 Opening Remarks:
Jon D. Moulton, Ph.D., Gene Tools, LLC
9:15 miRNA Expression Profiling Technologies and Research
Applications
Mike Wilson, Ph.D., Senior Scientist, Array R&D Manager,
Asuragen, Inc.
This workshop session will review the methods
and technologies for miRNA expression profiling. Methods for
quantitative recovery of small RNA species during RNA purification
will be presented, with particular attention to yields from whole
blood and formalin-fixed, paraffin-embedded (FFPE) tissues. A
survey of the current technology platforms for multiplex analysis
of miRNA expression profiling will be presented. Important
issues to consider with respect to data analysis and normalization
will be addressed.
9:45 High-Throughput Profiling of miRNAs in Neural
Stem Cells
Peng Jin, Ph.D., Assistant Professor, and Keith Szulwach,
Department of Human Genetics, Emory University School of Medicine
MicroRNAs have been implicated in the
maintenance and differentiation of stem cells. In this
presentation, we will discuss our work on high-throughput
profiling of miRNAs in neural stem cells using different
technologies.
10:15 Coffee Break
10:35 Whole miRNA/mRNA Profiling
from Single Embryonic Stem Cell and Early Embryos
Kai Q. Lao, Ph.D., Principal Scientist, Applied
Biosystems
We developed a real-time PCR-based, 330-plex miRNA,
expression profiling method that is sensitive and accurate
enough to profile miRNA from samples as small as a single
cell, such as an Embryonic stem cell. This technique will
greatly facilitate miRNA-related research on stem cells and
early embryos. It should also be of use in studies on
carcinogenesis where only limited amounts of material is
available from tissue biopsies or archived material.
11:05
Temporal Interference
of MicroRNA Maturation and in situ Labelling of miRNA in
Zebrafish Using Morpholino Oligonuceotides
Msc. Anne Karine Lagendijk, Hubrecht Institute Group: J. Bakkers,
Genetics of Cardiac Development
Few microRNA knockout studies have been reported; mutagenizing small
microRNA alleles is extremely difficult. Morpholino oligos are
efficient tools to temporally knock down single microRNAs in zebrafish
embryos, which revealed aberrant pancreatic islet development when
inhibiting miR-375. We also used Morpholinos to label microRNAs /in
situ/, demonstrating their versatility.
11:35 Technologies Q&A Panel Discussion
12:00pm End of Workshop
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