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              - Functions of Mitochondria
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                                1. Mitochondrial production of reactive oxygen species 1
- Prof. Martin Brand
 
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                                2. Mitochondrial production of reactive oxygen species 2
- Prof. Martin Brand
 
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                                3. Mitochondria and calcium signaling in cell life and cell death
- Prof. Michael R. Duchen
 
 - Mitochondrial Physiology
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                                6. Mitochondrial transporters and disease - function and mechanism
- Dr. Edmund R.S. Kunji
 
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                                7. Mitochondrial transporters and disease - structure and regulation
- Dr. Edmund R.S. Kunji
 
 - Mitochondrial DNA and Nuclear Genes Affecting Gene Expression
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                                8. Initiation and elongation of mammalian mitochondrial protein synthesis
- Dr. Linda L. Spremulli
 
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                                9. Human mitochondrial tRNAs: post-transcriptional modifications and diseases
- Prof. Tsutomu Suzuki
 
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                                10. Mitochondria and ageing in model systems
- Prof. Aleksandra Trifunovic
 
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                                11. Aetiology and molecular genetic basis of OXPHOS deficiencies
- Dr. Monika Winter
 
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                                13. Mitochondrial DNA mutations in cancer
- Dr. Laura Greaves
 
 
Printable Handouts
Navigable Slide Index
- Introduction
 - Lecture outline
 - Functions of cytosolic & nuclear Fe/S proteins
 - Fe/S protein biogenesis in "Amitochondriates"
 - Evolutionary origin of eukaryotic ISC machinery
 - Fe/S protein assembly without mitochondria
 - Cytosolic & nuclear Fe/S proteins & mISC
 - Yeast mitochondrial Atm1 structure
 - GSH is bound in a large hydrophilic cavity of Atm1
 - Biogenesis of cytosolic and nuclear Fe/S proteins
 - hCFD1-NBP35: required for FE/S protein assembly
 - Chaetomium thermophilum holo-Cfd1 structure
 - CIA machinery in yeast
 - CIA machinery in humans
 - Target specificity of human CIA proteins
 - Dedicated functions of human CIA targeting factors
 - The human CIA targeting factors
 - The numerous phenotypes of MMS19
 - Fe/S protein assembly and DNA damage
 - Fe/S protein biogenesis and genome integrity
 - Regulation of Fe/S protein biogenesis
 - Acknowledgements
 - References
 
Topics Covered
- Cytosolic and nuclear Fe/S proteins maturation
 - Role of mitochondria in cytosolic and nuclear Fe/S protein biogenesis
 - Functions of proteins involved in Fe/S protein biogenesis
 - Importance of Fe/S protein biogenesis for genome maintenance
 
Talk Citation
Lill, R. (2018, September 27). Biogenesis of cellular iron-sulfur proteins: the essential role of mitochondria and the CIA machinery [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved November 4, 2025, from https://doi.org/10.69645/BQSE9653.Export Citation (RIS)
Publication History
- Published on September 27, 2018
 
Financial Disclosures
- Prof. Roland Lill has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.
 
Biogenesis of cellular iron-sulfur proteins: the essential role of mitochondria and the CIA machinery
                  Published on September 27, 2018
                  
                    
                      
                        
                      
                    
                  
                  
                    36 min
                
              A selection of talks on Cell Biology
Transcript
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                  0:00
                
                
                  
                    Hello, my name is Roland Lill.
                  
                    I'm a professor of Cell Biology at
                  
                    the Institute for Zytobiologie at the Phillips-University of Marburg in Germany.
                  
                    This is the second part of my lecture on the biogenesis
                  
                    of cellular iron-sulfur proteins in eukaryotes.
                  
                    In part one, I've explained the process inside mitochondria.
                  
                    Now, in part two,
                  
                    I will focus on our current knowledge of
                  
                    the assembly pathways of iron-sulfur proteins in the cytosol and nucleus.
                  
                
              
                  0:32
                
                
                  
                    Here is a brief outline of my lecture.
                  
                    I will first explain why the mitochondria and the related organelles called mitosomes
                  
                    are essential for biogenesis of cytosolic and nuclear iron-sulfur proteins,
                  
                    including some interesting evolutionary aspects.
                  
                    Then, I will provide you with an overview of how
                  
                    cytosolic and nuclear iron-sulfur proteins are matured.
                  
                    Then, I will explain
                  
                    our current functional views on some of
                  
                    the components involved in the biogenesis in more detail.
                  
                    Finally, I will outline the importance of
                  
                    iron-sulfur protein biogenesis for genome maintenance.
                  
                
              
                  1:13
                
                
                  
                    In the first part of this lecture series,
                  
                    I have explained how
                  
                    the mitochondrial ISC assembly machinery assists
                  
                    with the maturation of iron-sulfur proteins within this organelle.
                  
                    I also told you already that the core of the ISC system is
                  
                    involved in the biogenesis of cytosolic and nuclear iron-sulfur proteins,
                  
                    in that it synthesizes an unknown sulfur-containing molecule X-S
                  
                    that is exported to the cytosol via the ABC transporter Atm1.
                  
                    In the cytosol, to so-called CIA or
                  
                    cytosolic iron-sulfur protein assembly machinery catalyzes
                  
                    the process and the 11 known CIA components and
                  
                    the mechanisms of this machinery will be the main topic of this part two of my lecture.
                  
                    Let us now look at which
                  
                    important iron-sulfur proteins are located in the cytosol and nucleus,
                  
                    and here I can give you only a small selection of these proteins.
                  
                    A famous cytosolic iron-sulfur protein mentioned already in part one is
                  
                    the iron regulatory protein 1 in its aconitase form.
                  
                    Two proteins involved in various aspects of protein translation are Rli1,
                  
                    which helps to separate the ribosomal subunits after
                  
                    translation termination and Tyw1 which is involved in tRNA nucleotide modification.
                  
                    In the cell nucleus,
                  
                    many enzymes involved in DNA maintenance contain iron-sulfur clusters.
                  
                    We have reported in 2012 that the replicative DNA polymerases,
                  
                    for instance, deltas contain
                  
                    functionally important iron-sulfur clusters at their C-termini.
                  
                    Moreover, various ATP-dependent DNA helicases involved in DNA repair,
                  
                    telomere length regulation, and chromosome segregation and
                  
                    many other aspects have been shown to contain iron-sulfur clusters.
                  
                    Malfunction of these proteins due to an impaired iron-sulfur cluster insertion is
                  
                    associated with different aspects of genome stability, which will be explained later in my lecture.
                  
                    All of these letter iron-sulfur enzymes and many more,
                  
                    are essential for cell viability,
                  
                    for instance, of yeast cells.
                  
                    In turn, this is the reason why mitochondria are essential in the eukaryotic cell.
                  
                    You may now argue that mitochondria are essential because of
                  
                    their most popular role in respiration or oxidative phosphorylation.
                  
                    However, it is well-known that yeast cells can live without
                  
                    active respiration as long as glucose is present as a fermentable carbon source.
                  
                    Likewise, the late Giuseppe Attardi has shown in the 1990s that
                  
                    also, human cells can live without
                  
                    mitochondrial DNA and thus, without active respiration,
                  
                    as long as high glucose is applied to the cells.
                  
                    This is different for the mitochondrial ISC system where
                  
                    most of the core IC genes are essential for cell viability.
                  
                    The reason for this is their role in extramitochondrial and sulfur protein biogenesis.
                  
                    A nice biological confirmation of this concept is provided by biology itself and will be
                  
                    discussed in the next slide because it shows that this process
                  
                    can also be the minimal function of the organelles.
                  
                
              
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