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Structural-functional studies of mitochondrial matrix proteins

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  • معلومة اضافية
    • بيانات النشر:
      Inst för cell- och molekylärbiologi / Dept of Cell and Molecular Biology
    • الموضوع:
      2018
    • Collection:
      Karolinska Institutet: Publications
    • نبذة مختصرة :
      The mitochondrion is the powerhouse of the eukaryotic cell. Most of the energy required to carry out cellular processes is generated inside mitochondria via the process of oxidative phosphorylation. The machinery required for oxidative phosphorylation is encoded by both the nuclear and the mitochondrial genome. The cellular energy production will thus collapse in the absence of mitochondrial gene expression. The mitochondrial RNA polymerase, POLRMT, together with two transcription factors, TFAM and TFB2m, initiate mitochondrial transcription. However, the exact mechanistic details of mitochondrial-transcription initiation are unclear. Furthermore, the transcription by POLRMT is non-processive, and it prematurely terminates after 150 nucleotides in a conserved sequence block region, CSBII. This indicates that accessory factors are required for a complete transcription event. In Paper I, we investigated the transcription initiation in mitochondria and proposed a model. In addition, we were able to demonstrate that an N-terminal extension (NTE) in POLRMT plays a role in the transition from the initiation to the elongation phase, possibly by undergoing a conformational change. Upon the deletion of NTE, the POLRMT is hyperactive, and together with TFB2m, it can carry out non-specific transcription events. Thus, we conclude that the NTE is necessary for promoter-specific transcription initiation. Once the transcription is initiated, the POLRMT enters the elongation phase. In Paper II, we were able to characterize the in-vitro role of a transcription-elongation factor, TEFM. TEFM increases the processivity of the POLRMT by allowing it to bypass road blocks, such as the CSBII, and DNA lesions, such as apurinic or apyrimidinic sites. We furthermore suggested that TEFM may be involved in the regulation of mitochondrial transcription and replication in mammalian mitochondria. For mitochondrial homeostasis, the integrity of proteins in the mitochondrial matrix must be maintained, and this is achieved through the ...
    • File Description:
      application/pdf
    • Relation:
      I. The amino terminal extension of mammalian mitochondrial RNA polymerase ensures promoter specific transcription inititiation. Posse V, Hoberg E, Dierckx A, Shahzad S, Koolmeister C, Larsson NG, Wilhelmsson LM, Hällberg BM and Gustafsson C. Nucleic Acids Research. 2014, 42; 3638-3647. ::doi::10.1093/nar/gkt1397 ::pmid::24445803 ::isi::000334758600023; II. TEFM is a potent stimulator of mitochondrial transcription elongation invitro. Posse V, Shahzad S, Falkenberg M, Hällberg BM and Gustafsson CM. Nucleic Acids Research. 2015, 43:2615-24. ::doi::10.1093/nar/gkv105 ::pmid::25690892 ::isi::000352487100018; III. Structure and degradation mechanism of the Human Mitochondrial Lon protease. Shahzad S, Hernandez CP, Falkenberg M and Hällberg BM. [Manuscript]; http://hdl.handle.net/10616/46506
    • الدخول الالكتروني :
      http://hdl.handle.net/10616/46506
    • Rights:
      info:eu-repo/semantics/openAccess
    • الرقم المعرف:
      edsbas.3D77B878