Laboratory
of RNA Biology
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We are interested in understanding how the different fragments of a gene are selectively combined (spliced) to produce multiple products in biology and diseases. |
This process, called pre-mRNA splicing, has profound implications in the evolution and functional complexity of genes/gene products. Its disruption is a cause of human genetic diseases by many mutations and also of the aberrant splicing in cancers. Our past research has focused on the molecular basis of adaptive splicing, likely involved in cell adaptation, neuron homeostasis and neurological diseases. This has also allowed us to discover and extend the scope to a novel class of introns/splice sites (REPA-harbouring) contributing to the evolution of alternative splicing, gene product diversity or to the prevention of aberrant splicing in human health/diseases. Here are more DETAILS. Particularly welcome to join us are students with backgrounds in biochemistry, genetics, computer science or statistics. |
The REPAG element specifically
among mammals |
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The CaRRE element among
vertebrates (Liu GD, et al., J. Biol.
Chem. 2012, 287:22709–22716) |
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A new group of
introns: REPA element 'inserted' between the
Py and 3'AG and its effects on alternative
splicing |
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Misce. links:
Faculty of Graduate Studies |
Department of Physiology & Pathophysiology |
College of Medicine |
Faculty of Health Sciences |
University of Manitoba |