Thinking of doing your PhD in the Life Sciences? The International PhD Programme (IPP) Mainz is offering talented scientists the chance to work on cutting edge research projects within the open call on “Molecular Mechanisms in Genome Stability & Gene Regulation”. As an IPP PhD student, you will join a community of exceptional scientists working on diverse topics ranging from how organisms age or how our DNA is repaired, to how epigenetics regulates cellular identity or neural memory.
For more details on the projects offered and how to apply via the online form using the apply button.
The deadline for applications is 1 April 2026. Interviews will take place at IMB in Mainz on 22 & 23 June 2026.
Starting date: 1 July - 31 December 2026
PhD Position: Molecular interactions in the mammalian circadian clock (m/f/d)
Activities and responsibilities
The research group of Eva Wolf offers the following PhD project:
Many physiological processes are regulated in a day-time dependent (circadian) manner. In the primary gene regulatory feedback loop of the mammalian circadian clock, the transcription factors CLOCK and BMAL1 activate the expression of PERIOD (PER1,2,3) and Cryptochrome (CRY1,2) clock proteins, which feedback-repress CLOCK/BMAL1. Within a 24h day, CLOCK/BMAL1 cycles between an active state recruiting co-activators like MLL1, an early repressed state including CRY1/2, PER, CK1 kinase and other proteins, and a late repressed state where only CRY1 remains associated with CLOCK/BMAL1. Additionally, cytosolic CRY/PER/CK1 containing complexes are formed before the proteins enter the nucleus in a time-regulated manner. In a secondary feedback loop, the circadian expression of Bmal1 is regulated by the nuclear receptors REV-ERB and ROR.
PhD project: 3D structural and molecular mechanistic analyses of PERIOD protein interactions in the mammalian circadian clock
This PhD project aims to characterize the dynamically changing protein interactions of PERIOD clock proteins in the context of cytosolic or nuclear PER/CRY/CK1 containing complexes, employing in vitro protein biochemistry, high resolution 3D structure determination by X-ray crystallography or Cryo-EM, quantitative/biophysical protein interaction studies, spectroscopy and molecular biology. We recently showed that WDR5, a component of the CLOCK/BMAL1 co-activating MLL1 histone-methyltransferase complex, also forms a PER1/WDR5 complex, that affects circadian oscillations (publication under revision). In this PhD project the interactions between PER1, WDR5 and the REV-ERB/ROR nuclear receptors will be further investigated on a molecular mechanistic and 3D structural level to understand how the PER1/WDR5 complex impacts the primary and secondary feedback loop of the mammalian circadian clock. The PhD candidate will also further investigate the interaction interplay of PERIOD proteins with other protein components of CRY/PER/CK1 containing complexes. We are looking for a highly motivated PhD candidate with a strong interest in structural biology of proteins, protein biochemistry- and biophysics, and significant previous exposure to these areas during their bachelor/master education.
If you are interested in this project, please select Wolf as your group preference in the IPP application platform.
Many physiological processes are regulated in a day-time dependent (circadian) manner. In the primary gene regulatory feedback loop of the mammalian circadian clock, the transcription factors CLOCK and BMAL1 activate the expression of PERIOD (PER1,2,3) and Cryptochrome (CRY1,2) clock proteins, which feedback-repress CLOCK/BMAL1. Within a 24h day, CLOCK/BMAL1 cycles between an active state recruiting co-activators like MLL1, an early repressed state including CRY1/2, PER, CK1 kinase and other proteins, and a late repressed state where only CRY1 remains associated with CLOCK/BMAL1. Additionally, cytosolic CRY/PER/CK1 containing complexes are formed before the proteins enter the nucleus in a time-regulated manner. In a secondary feedback loop, the circadian expression of Bmal1 is regulated by the nuclear receptors REV-ERB and ROR.
PhD project: 3D structural and molecular mechanistic analyses of PERIOD protein interactions in the mammalian circadian clock
This PhD project aims to characterize the dynamically changing protein interactions of PERIOD clock proteins in the context of cytosolic or nuclear PER/CRY/CK1 containing complexes, employing in vitro protein biochemistry, high resolution 3D structure determination by X-ray crystallography or Cryo-EM, quantitative/biophysical protein interaction studies, spectroscopy and molecular biology. We recently showed that WDR5, a component of the CLOCK/BMAL1 co-activating MLL1 histone-methyltransferase complex, also forms a PER1/WDR5 complex, that affects circadian oscillations (publication under revision). In this PhD project the interactions between PER1, WDR5 and the REV-ERB/ROR nuclear receptors will be further investigated on a molecular mechanistic and 3D structural level to understand how the PER1/WDR5 complex impacts the primary and secondary feedback loop of the mammalian circadian clock. The PhD candidate will also further investigate the interaction interplay of PERIOD proteins with other protein components of CRY/PER/CK1 containing complexes. We are looking for a highly motivated PhD candidate with a strong interest in structural biology of proteins, protein biochemistry- and biophysics, and significant previous exposure to these areas during their bachelor/master education.
If you are interested in this project, please select Wolf as your group preference in the IPP application platform.
Qualification profile
Are you an ambitious scientist looking to push the boundaries of research while interacting with colleagues from multiple disciplines and cultures? Then joining the IPP is your opportunity to give your scientific career a flying start!
All you need is:
All you need is:
- Master or equivalent
- Interactive personality & good command of English
- 2 letters of reference
We offer
- Exciting, interdisciplinary projects in a lively international environment, with English as our working language
- Advanced training in scientific techniques and professional skills
- Access to our state-of-the-art Core Facilities and their technical expertise
- Fully funded positions with financing until the completion of your thesis
- A lively community of more than 200 PhD students from 44 different countries
For more details on the projects offered and how to apply via the online form using the apply button.
The deadline for applications is 1 April 2026. Interviews will take place at IMB in Mainz on 22 & 23 June 2026.
Starting date: 1 July - 31 December 2026
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