Science University Research Symposium (SURS)

Analyzing Dbp5 Residues Required for Interaction with Nab2

Publication Date



Sciences and Mathematics, College of


Biology, Department of

SURS Faculty Advisor

Rebecca Adams, Ph.D.

Presentation Type

Poster Presentation


In Saccharomyces cerevisiae, as in all eukaryotes, mature mRNA exits the nucleus following transcription to permit translation in the cytoplasm in a process called mRNA export. To allow for transcript export, the RNA Binding Protein Nab2 binds to the poly-A tail and recruits RNA export protein Mex67 to allow the transcript to cross the nuclear pore complex. To prohibit mRNA entry back into the nucleus, the protein Dbp5 removes these proteins from the transcript through ATPase activity, allowing Nab2 and Mex67 to recycle back into the nucleus. It is unknown how Dbp5 specifically removes Nab2 and Mex67 and not the other RBPs that bind to the transcript in the nucleus and are maintained in the cytoplasm. I hypothesize that Dbp5 binds to Nab2 and/or Mex67, bringing Dbp5 to the region of the transcript where they bind for removal. Supporting this hypothesis, the interaction between Dbp5 and Nab2 can be observed using a split-Venus approach which not only displays fluorescence but also results in cell death. My goal is to use the split-Venus interaction to identify the Dbp5-Nab2 interface. To do this, I performed a random mutagenesis to generate random mutations within Dbp5, of which some might prohibit the interaction between Dbp5 and Nab2. This library of mutants will then be transformed into Nab2-VN to uncover viable mutants, indicating a potential disrupted interaction. These mutants will then be screened and sequenced to identify the mutation site. We anticipate that these results will aid in understanding Dbp5 selectivity.

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