Maria Zapp, Ph.D.
Academic Role: Assistant Professor
Faculty Appointment(s) In:
Molecular Genetics and Microbiology
Program in Molecular Medicine
Other Affiliation(s):
Cancer Center
Center for AIDS Research
Interdisciplinary Graduate Program
Program in Immunology and Virology
Regulation of retroviral and cellular mRNA transport
Studies in this laboratory focus on the regulation of gene expression at
the level of RNA nucleocytoplasmic transport. As a model system for
studying nuclear RNA export, we are analyzing the mechanism of action of
the novel HIV-1 Rev protein. This sequence-specific RNA binding protein
faciliates the redistribution of HIV-1 mRNAs that encode the viral
structural protein from the nucleus to the cytoplasm. Atypical of
cellular mRNAs, the gag-pol and env mRNAs leave
the nucleus partially or completely unspliced. The molecular mechanism by
which Rev mediates nucleocytoplasmic events remains unknown. Previous
studies by several laboratories have shown that Rev function requires
minimally a cis-acting sequences within the second intron of the viral
pre-mRNAs, the Rev Responsive Element or "RRE" ; and
a well-defined "effector" domain located at the carboxy-terminal portion
of the protein. Recent studies have also identified a human
nuclear-specific protein, hRIP, that interacts directly with the effector
domain of Rev. The hRIP polypeptide is one possible candidate for a
cellular factor that mediates Rev function. Moreover, in the absence of
Rev, hRIP may play an important role in the nucleocytoplasmic transport of
cellular RNAs. The identification and characterization of this cellular
protein significantly enhances our ability to analyze the molecular
details of Rev function and ultimately, cellular factors that mediate
cellular nuclear RNA export.
We are currently using biochemical and Xenopus laevis
oocyte microinjection approaches to identify other cellular components
that are required for Rev function. We have recently developed a novel
in vitro nuclear RNA export assay to study cellular and viral
nuclear RNA export in mammalian cells. Initially, we will use this assay
system to probe Rev's mechanism of action. However, we anticipate that
our in vitro nuclear RNA export assay will be a very useful
tool for defining cellular factors that facilitate nuclear export of
various classes of nuclear RNAs. Defining the functional role of these
cellular components will provide needed insights into the molecular
mechanism(s) of nuclear RNA export.
Office: B2-207
Phone: 508-856-4787
E-mail: Maria.Zapp@umassmed.edu
Keywords:
Gene Expression
Postdoctoral Position Available
A postdoctoral position is available to study in this laboratory.
Contact Dr. Zapp for additional details.
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