Identification of novel FANCD2 interacting proteins via immunoprecipitation and mass spectrometry

Paul A Azzinaro, University of Rhode Island

Abstract

Fanconi Anemia (FA) is a rare genetic disease caused by biallelic mutations in one of sixteen genes involved in the FA-BRCA DNA damage repair pathway. The proteins encoded by these genes function cooperatively in a common pathway which resolves lesions caused by interstrand crosslinks (ICLs). A critical step in this pathway is the monoubiquitination and chromatin targeting of FANCD2 and FANCI. The mechanism by which these proteins are targeted to chromatin is not understood. FANCD2 is known to interact with several downstream proteins while associated with chromatin. Finding new FANCD2 interacting proteins is critical to understanding how FANCD2 functions and how it is regulated within the cell. Several candidate interacting proteins have been identified by immunoprecipitations (IPs) coupled with mass spectrometry. Candidates include transcription factors, chromatin remodeling complex components and proteins involved in chromosome maintenance and stability. These interactions are being validated and functionally characterized using a variety of techniques.^

Subject Area

Biology, Cell|Chemistry, Biochemistry

Recommended Citation

Paul A Azzinaro, "Identification of novel FANCD2 interacting proteins via immunoprecipitation and mass spectrometry" (2014). Dissertations and Master's Theses (Campus Access). Paper AAI1570638.
http://digitalcommons.uri.edu/dissertations/AAI1570638

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