PhD Scientific Days 2018

Budapest, 19-20 April 2018

Poster presentations: Molecular medicine

RAS-mediated Pathways in the Metabolic Regulation of the Circadian Clock

Előadó neve

Szőke, Anita

Előadó munkahelye

Department of Physiology, Semmelweis University

Előadó telefonszáma

+36 1 459-1500/60412

Előadó e-mail címe

szoke.anita@med.semmelweis-univ.hu

Az előadás címe

RAS-mediated Pathways in the Metabolic Regulation of the Circadian Clock

Szerző(k) neve és munkahelye

Anita Szőke1, Norbert Gyöngyösi1, Krisztina Ella1, Ágnes Sűdy1 and Krisztina Káldi1,2
1Department of Physiology, Semmelweis University, Budapest
2Department of Laboratory Medicine, Semmelweis University, Budapest

Bemutatás módja

Poszter

Szekció

Poster presentations: Molecular medicine

Language of the presentation

English

Témacsoport

molecular sciences

Összefoglaló szövege

The metabolic regulation of the circadian clock has been investigated for a long time, however the underlying mechanism is still not completely understood. Metabolic compensation allows the circadian oscillator to keep a nearly constant period in an environment with changing substrate levels.

As RAS2-mediated signalling plays a central role in the adaptation of yeast to different nutritional environments, we examined the involvement of the RAS-mediated pathway in the metabolic regulation of the clock in the circadian model organism Neurospora crassa. We found that in the ras2-deficient strain the period was longer than in the control and operation of the circadian clock was affected by glucose. In contrast to the wt, in ∆ras2 the period become longer and the oscillation of the expression of the frequency (frq) gene showed dampening in the presence of glucose. In accordance with the longer period and the less robust rhythm of the mutant, both phosphorylation and nuclear clearance of the FRQ protein were delayed in constant darkness. Whereas glucose did not affect the subcellular distribution of FRQ in wt, elevated FRQ levels were detected in Δras2 nuclei. Interaction of RAS2 with the RAS-binding domain of the adenylate cyclase in vitro and the ability of a cAMP analogue to rescue the circadian phenotype of the mutant strain suggested that RAS2 acting via a cAMP-dependent pathway exerts metabolic control on the Neurospora circadian clock.

To further investigate the role of RAS-mediated pathways in the metabolic regulation of the clock, we also examined the circadian phenotype of a ∆rasgef strain. We found that under light-dark conditions, the phase of conidiation was delayed compared to the wt and expression of the rasgef gene was affected by glucose.

Our data indicate that RAS-mediated pathways play an important role in the metabolic compensation of the circadian clock in Neurospora crassa.

Data of the presenter

Doctoral School: Doctoral School of Molecular Medicine
Program: Cellular and Molecular Physiology
Supervisor: Krisztina Káldi
E-mail address: szoke.anita@med.semmelweis-univ.hu

Kind

Szabad

Status

elfogadva

Accepted presentation method

poszter

Előadás fájl jóváhagyás

nem rendelkezett róla

Előadó

2921

Presentation file URL

//docs.kmcongress.com/phd2018/eposter_4271.png

Authors (legacy)

Anita Szőke1, Norbert Gyöngyösi1, Krisztina Ella1, Ágnes Sűdy1 and Krisztina Káldi1,2
1Department of Physiology, Semmelweis University, Budapest
2Department of Laboratory Medicine, Semmelweis University, Budapest