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Investigation of Fanconi Anemia Protein Interactions by Yeast Two-Hybrid Analysis

Authors
  • Huber, Pia A.J.
  • Medhurst, Annette L.
  • Youssoufian, Hagop
  • Mathew, Christopher G.
Type
Published Article
Journal
Biochemical and Biophysical Research Communications
Publication Date
Jan 01, 2000
Volume
268
Issue
1
Pages
73–77
Identifiers
DOI: 10.1006/bbrc.1999.2055
Source
Elsevier
Keywords
License
Unknown

Abstract

Fanconi anemia is a chromosomal breakage disorder with eight complementation groups (A–H), and three genes ( FANCA, FANCC, and FANCG) have been identified. Initial investigations of the interaction between FANCA and FANCC, principally by co-immunoprecipitation, have proved controversial. We used the yeast two-hybrid assay to test for interactions of the FANCA, FANCC, and FANCG proteins. No activation of the reporter gene was observed in yeast co-expressing FANCA and FANCC as hybrid proteins, suggesting that FANCA does not directly interact with FANCC. However, a high level of activation was found when FANCA was co-expressed with FANCG, indicating strong, direct interaction between these proteins. Both FANCA and FANCG show weak but consistent interaction with themselves, suggesting that their function may involve dimerisation. The site of interaction of FANCG with FANCA was investigated by analysis of 12 mutant fragments of FANCG. Although both N- and C-terminal fragments did interact, binding to FANCA was drastically reduced, suggesting that more than one region of the FANCG protein is required for proper interaction with FANCA.

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