神经退行性疾病的分子机制博士研究员(科研助理)

PhD position: Molecular mechanisms of neurodegenerative diseases (m/f/d)

Institute of Molecular Biology gGmbH (IMB) · 德国 · Mainz

原帖优先:申请材料、截止时间与资格以原帖和学校官方说明为准。

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研究内容
该项目旨在探索FUS和TDP-43在R-loop调控和基因组稳定性中的作用。
申请条件
硕士学位,英语良好,2封推荐信。
待遇
全额资助,直到完成论文。
申请方式
申请截止日期:2026年10月15日,面试时间:2027年1月18-19日,开始日期:2027年2月1日-7月31日。申请材料:动机信、简历、证书、成绩单、推荐信。
材料清单
  • 动机信
  • 简历
  • 证书
  • 成绩单
  • 推荐信

由 @cf/meta/llama-3.3-70b-instruct-fp8-fast 生成,博士岗判定置信度 100%。

岗位信息

截止
(Europe/Berlin) 剩 4 天
学科
神经科学
合同类型
雇佣合同
本站收录
内容更新
入职
2027-02-01
导师
Dorothee Dormann
来源
DAAD PhDGermany 博士岗位与项目 · 最近核对 2026-10-11
详情核验
判定依据(原文摘录)
  • is_phd
    PhD position: Molecular mechanisms of neurodegenerative diseases (m/f/d)
原文

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PhD position: Molecular mechanisms of neurodegenerative diseases (m/f/d) Full PhD Working Language English

Location Mainz

Application Deadline 15. Oct 2026

Starting Date 01. Feb 2027

• Overview • Description • Required Documents • Application

Overview Open Positions 1

Time Span 01. Feb 2027 for 3 years

Application Deadline 15. Oct 2026

Financing yes

Type of Position Full PhD

Working Language English

Required Degree Master

Areas of study Biology, Molecular Biology, Neuroscience

Description Description 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 . 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. R-loops occur naturally during transcription and can have important regulatory functions, however, persistence of R-loops can have deleterious effects and result in the accumulation of DNA double-strand breaks and genome instability. DNA damage and aberrant R-loops have been linked to human diseases, including neurodegenerative disorders. For instance, several genes that are mutated in the neurodegenerative diseases amyotrophic lateral sclerosis (ALS) and frontotemporal dementia (FTD) have been implicated in DNA damage repair and the regulation of R-loops, suggesting that DNA damage and genome instability may contribute to neurodegeneration in these disorders. Two of these ALS/FTD-associated genes encode for the major aggregating proteins in ALS and FTD patients, TAR DNA binding protein of 43 kDa (TDP-43) and Fused in Sarcoma (FUS). They are ubiquitously expressed DNA/RNA-binding proteins that are normally predominantly localized in the nucleus. However, in the degenerating brain regions of ALS and FTD patients, TDP-43 and FUS are largely absent from the nucleus and accumulate in cytosolic aggregates of neurons and glial cells, resulting in a loss of nuclear TDP-43 or FUS function. TDP-43 or FUS depletion by RNA interference causes DNA damage and R-loop accumulation and DNA damage markers are elevated in brains of ALS/FTD patients. The molecular mechanisms by which TDP-43 and FUS contribute to DNA repair and suppress R-loops are largely unknown.

PhD project: Role of FUS and TDP-43 in R-loop regulation and genome stability

This project seeks to unravel the molecular mechanisms by which FUS and TDP-43 contribute to R-loop suppression and DNA repair, using a combination of in vitro and cellular model systems. Questions that we would like to address include: 1. How does the protein interactome of FUS and TDP-43 get rewired upon DNA damage? 2. Is their phase separation/condensation behavior or their ability to bind to DNA/RNA required for R-loop suppression or their recruitment to damage sites? 3. How do post-translational modifications, e.g. ADP-ribosylation and phosphorylation, regulate FUS or TDP-43’s function in R-loop suppression and the DNA damage response? 4. Where in the genome do R-loops appear upon FUS or TDP-43 loss-of-function? The project involves a wide methods spectrum, ranging from proximity proteomics, over molecular cell biology (advance fluorescence microscopy, live cell imaging) to protein biochemistry ( in vitro assays with recombinant proteins) and the possibility to learn and apply genome-wide R-loop mapping techniques.

This project will be part of the RTG on R-loop Regulation in Robustness and Resilience (4R). More information can be found at: Project 6. R-loop regulation by neurodegeneration-linked DNA/RNA-binding proteins FUS and TDP-43. - 4R-RTG ( https://4r-rtg.de/portfolio/dormann/ )

If you are interested in this project, please select Dormann 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: • 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 ofmore 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 15 October 2026. Interviews will take place at IMB in Mainz on 18+19 January 2027. Starting date: 1 February - 31 July 2027

Required Documents Required Documents • Motivation letter • CV • Certificates • Transcripts • References

Application Application

https://www.imb.de/students-postdocs/international-phd-programme/apply-to-ipp/projects-offered/dorothee-dormann

https://www.imb.de/phd Contact Institute of Molecular Biology gGmbH (IMB) International PhD Programme (IPP) Mainz Address Street Ackermannweg 4 Zipcode 55128 City Mainz

Contact details Web: https://www.imb.de/phd

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