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Kevin Czaplinski, PhD
Assistant Professor
Department of Biochemistry and Cell Biology
Life Science Building, CMM 542
Stony Brook University
Stony Brook, NY 11794-5215
Office telephone: 631-632-8635
E-mail: Kevin.Czaplinski@stonybrook.edu
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Research Description |
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Post-transcriptional control of gene expression in the nervous system
In many
instances cells rely on post-transcriptional processes to regulate gene expression
very rapidly and locally within the cytoplasm. Translation, localization and
degradation of messenger RNA (mRNA) within the cytoplasm are all processes
that can coordinate to achieve dynamic control of gene expression. Post-transcriptionally
induced changes in gene expression are thought to be mediated through the large
Ribonucleo-Protein Complexes (RNPs) that form on each mRNA, called mRNPs, but
our understanding of how these regulatory units function is poor.
My lab focuses on post-transcriptional control of gene expression, particularly
on localization of mRNA within the cytoplasm, one poorly understood component
of post-transcriptional regulation. Active localization of mRNA is particularly
important to the nervous system where the cell cytoplasm can extend great distances
away from the nucleus. At these distances, diffusion of products produced within
the cell soma will not suffice to supply proteins to the neuronal cellular
periphery that are needed for cell maintenance and function, synaptogenesis
and synaptic plasticity. Cells must actively transport these factors to remote
locations, and transporting mRNA in neurons is one means to achieve this. Because
mRNA is the template for translation, mRNA localization directs protein synthesis
to the distal regions of the cytoplasm where the product will function.
Identification of Transport RNPs in Neurons
My studies take complementary approaches to understand the formation and function
of RNP complexes involved in localizing mRNA in neurons. To localize mRNA within
the cytoplasm, specific cis-acting sequences within an mRNA are recognized
by RNA binding proteins to coordinate formation of the RNP. This RNP
interacts with the cytoskeleton as well as with membrane associated signaling
complexes to achieve translation of the mRNA at the right time and place within
the cytoplasm. Many unanswered questions remain about the roles of most of
these RNP components. We are performing studies that will examine the roles
of the RNA binding proteins as well as the sequence elements involved in localizing
mRNA to the processes of neurons. Several neurological diseases including mental
retardation involve mis-regulation of mRNA in the cytoplasm and we believe
that understanding these mechanisms will lead to novel therapeutic approaches
to treat these diseases.

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