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Interferon-inducible protein 16: insight into the interaction with tumor suppressor p53.


ABSTRACT: IFI16 is a member of the interferon-inducible HIN-200 family of nuclear proteins. It has been implicated in transcriptional regulation by modulating protein-protein interactions with p53 tumor suppressor protein and other transcription factors. However, the mechanisms of interaction remain unknown. Here, we report the crystal structures of both HIN-A and HIN-B domains of IFI16 determined at 2.0 and 2.35 Å resolution, respectively. Each HIN domain comprises a pair of tightly packed OB-fold subdomains that appear to act as a single unit. We show that both HIN domains of IFI16 are capable of enhancing p53-DNA complex formation and transcriptional activation via distinctive means. HIN-A domain binds to the basic C terminus of p53, whereas the HIN-B domain binds to the core DNA-binding region of p53. Both interactions are compatible with the DNA-bound state of p53 and together contribute to the effect of full-length IFI16 on p53-DNA complex formation and transcriptional activation.

SUBMITTER: Liao JC 

PROVIDER: S-EPMC3760383 | biostudies-literature | 2011 Mar

REPOSITORIES: biostudies-literature

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Interferon-inducible protein 16: insight into the interaction with tumor suppressor p53.

Liao Jack C C JC   Lam Robert R   Brazda Vaclav V   Duan Shili S   Ravichandran Mani M   Ma Justin J   Xiao Ting T   Tempel Wolfram W   Zuo Xiaobing X   Wang Yun-Xing YX   Chirgadze Nickolay Y NY   Arrowsmith Cheryl H CH  

Structure (London, England : 1993) 20110301 3


IFI16 is a member of the interferon-inducible HIN-200 family of nuclear proteins. It has been implicated in transcriptional regulation by modulating protein-protein interactions with p53 tumor suppressor protein and other transcription factors. However, the mechanisms of interaction remain unknown. Here, we report the crystal structures of both HIN-A and HIN-B domains of IFI16 determined at 2.0 and 2.35 Å resolution, respectively. Each HIN domain comprises a pair of tightly packed OB-fold subdom  ...[more]

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