FP6Reintegration grant2006–2008

IOIDMC · Identification of interacting domain of mammalian cryptochrome with clock proteins, BMAL, Period, and CLOCK

FP6 — Marie Curie Actions (Human Resources and Mobility)

Duration
2006-05-01 → 2008-04-30
EU contribution
€80,000
Participants
1
Scheme
IRG

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Results in brief

Final Activity Report Summary - IOIDMC (Identification of interacting domain of mammalian cryptochrome with clock proteins, BMAL, Period, and CLOCK)

Circadian rhythms are the endogenous oscillations that occur with a periodicity of approximately 24 hours, and which regulate the biochemical and behavioural functions of organisms. Theses rhythms are achieved by the CLOCK proteins, which are located in the suprachiasmatic nuclei (SCN). The clockwork is made up of positive and negative transcriptional regulators. The CLOCK-BMAL1 heterodimer activates transcription of the period 2 (PER2) and CRY2 genes. The PER proteins interact with the CRY proteins; central sequences of the PER proteins interact with CKIe, and the resulting ternary complexes translocate into the nucleus, where they negatively regulate the transcription of PER and CRY genes. The PER and CRY proteins also positively regulate transcription of Bmal1. In this study, the interacting domain of cryptochromes with BMAL and PER2 has been identified using a mammalian two-hybrid system. Our results indicated that in mice CRY2 carboxyl termini are responsible for the interactions with PER2. Further analysis has indicated one amino acid Arg is responsible for this interaction with PER2. Also, Analyses of Cryptochrome domain that participate interaction with BMAL1 revealed that both C- and N-termini participate such interaction. All these results can be utilised for the drug discovery against biological clock related diseases.

Data: CORDIS, © European Union

Project objective

Cryptochromes are flavin- and folate-containing proteins with a high degree of similarity to DNA photolyase, which repairs UV-induced DNA damage. Cryptochrome play essential roles in the maintenance of circadian rhythms in mice and human. A transcription-translational feedback loop has been shown to be essential component of clock, and this mechanism seems to be conserved over a wide range of species. The transcriptional activation by CLOCK: BMAL1 heterodimer and inhibition by Cryptochrome and PERIOD are believed to provide the framework of the feedback loop in mammals. With this project interacting domain of mammalian cryptochrome with clock proteins will be identified by mammalian two-hybrid system and co-immuno precipitation assay.

Original text from CORDIS.

Participants

  • KOÇ UNIVERSITY · ISTANBULCoordinatorTürkiye

Links

Data: CORDIS, © European Union