idw – Informationsdienst Wissenschaft

Nachrichten, Termine, Experten

Grafik: idw-Logo
Science Video Project
idw-Abo

idw-News App:

AppStore

Google Play Store



Instance:
Share on: 
03/10/2022 15:55

Rear-end Collision on the “Ribosome Highway”

Marietta Fuhrmann-Koch Kommunikation und Marketing
Universität Heidelberg

    As a molecular machine found in the cells of all organisms, the ribosome is responsible for making new proteins. For a number of reasons, this process can fail, leaving the ribosome stalled on the mRNA and bringing synthesis of the protein to a halt. An international research team led by scientists from Heidelberg University has now identified a bacterial protein called MutS2 that senses and rescues these stuck protein factories.

    Press Release
    Heidelberg, 10 March 2022

    Rear-end Collision on the “Ribosome Highway”
    Researchers identify bacterial protein that senses and rescues “stalled” ribosomes

    As a molecular machine found in the cells of all organisms, the ribosome is responsible for making new proteins. It reads the blueprint for a certain protein on a messenger molecule – known as messenger RNA (mRNA) – and then converts this information into new proteins. For a number of reasons, this process can fail, leaving the ribosome stalled on the mRNA and bringing synthesis of the protein to a halt. An international research team led by scientists from the Center for Molecular Biology of Heidelberg University (ZMBH) has now identified a bacterial protein called MutS2 that senses and rescues these stuck protein factories. The fact that the next ribosome on the mRNA chain collides with the stalled ribosome plays a key role.

    The blueprints of proteins are stored in the DNA in the cell nucleus, where they are transcribed into mRNA. Bearing the genetic information for a specific protein, the mRNA leaves the nucleus and is transported to the ribosomes, where its information is converted into proteins. “Sometimes ribosomes can get stuck reading the blueprints owing to a defective mRNA molecule, for instance. This is particularly problematic because unfinished proteins are potentially toxic to the cell,” explains ZMBH molecular biologist and working group leader Prof. Dr Claudio Joazeiro. “That is why cells have developed mechanisms that detect stalled ribosomes and mark the incomplete proteins for destruction while still in their birthplace, the ribosome.”

    Using high-resolution cryo-electron microscopy, the researchers decoded a major step in this process with the aid of the common soil bacterium, Bacillus subtilis. They were able to precisely characterise how the MutS2 protein, found in nearly one third of all bacteria species, senses stalled ribosomes. MutS2 detects the collision between the stuck ribosome and the next one on the mRNA – a process which ZMBH junior research group leader Dr Stefan Pfeffer likens to a rear-end collision caused by a stalled vehicle on the highway, thus catching the attention of the police.

    To rescue ribosomes stuck on the mRNA, MutS2 follows two independent strategies, according to the researchers. “On one hand, MutS2 cuts the mRNA molecule, which subjects it to degradation. On the other hand, MutS2 separates the ribosome into its two subunits, so that it can be recycled for later rounds of protein synthesis. At the same time, the so-called ribosome-associated protein quality control marks the unfinished protein for destruction,” explains Dr Pfeffer. Prof. Joazeiro emphasises that this quality control mechanism is conserved from bacteria to humans. “We thus expect that the understanding of this fundamental process in bacteria will shed light on disease mechanisms in mammals, where failure to degrade unfinished proteins is associated with neurodegeneration and neuromuscular diseases,” adds the researcher.

    In addition to the ZMBH researchers from Heidelberg, scientists from the University of Cologne as well as Scripps Research in Florida (USA) also participated in the study. Funding was provided by the US National Institute of Neurological Disorders and Stroke, the German Research Foundation, the European Union in the context of “Horizon 2020”, the Aventis Foundation and the Chica and Heinz Schaller Foundation. The results of the study were published in the journal “Nature”.

    Contact:
    Heidelberg University
    Communications and Marketing
    Press Office, phone +49 6221 54-2311
    presse@rektorat.uni-heidelberg.de


    Contact for scientific information:

    Dr Stefan Pfeffer
    Center for Molecular Biology of Heidelberg University
    Phone +49 6221 54-6893
    s.pfeffer@zmbh.uni-heidelberg.de

    Prof. Dr Claudio Joazeiro
    Center for Molecular Biology of Heidelberg University
    Phone +49 6221 54-6858
    c.joazeiro@zmbh.uni-heidelberg.de


    Original publication:

    F. Cerullo, S. Filbeck, P. R. Patil, H.-C. Hung, H. Xu, J. Vornberger, F. W. Hofer, J. Schmitt, G. Kramer, B. Bukau, K. Hofmann, S. Pfeffer, C. A. P. Joazeiro: Bacterial ribosome collision sensing by a MutS DNA repair ATPase paralogue. Nature (9 March 2022), DOI: 10.1038/s41586-022-04487-6


    More information:

    http://www.zmbh.uni-heidelberg.de/Pfeffer/default.shtml - Pfeffer Working Group
    http://www.zmbh.uni-heidelberg.de/Joazeiro/default.shtml - Joazeiro Working Group


    Images

    Cryo-EM structure of the collided ribosomes with MutS2. Molecular components were coloured differently (stalled ribosome: orange; collided ribosome: green; MutS2: blue; mRNA: pink).
    Cryo-EM structure of the collided ribosomes with MutS2. Molecular components were coloured different ...

    Sebastian Filbeck (ZMBH)


    Criteria of this press release:
    Journalists, Scientists and scholars
    Biology
    transregional, national
    Research results, Scientific Publications
    English


     

    Cryo-EM structure of the collided ribosomes with MutS2. Molecular components were coloured differently (stalled ribosome: orange; collided ribosome: green; MutS2: blue; mRNA: pink).


    For download

    x

    Help

    Search / advanced search of the idw archives
    Combination of search terms

    You can combine search terms with and, or and/or not, e.g. Philo not logy.

    Brackets

    You can use brackets to separate combinations from each other, e.g. (Philo not logy) or (Psycho and logy).

    Phrases

    Coherent groups of words will be located as complete phrases if you put them into quotation marks, e.g. “Federal Republic of Germany”.

    Selection criteria

    You can also use the advanced search without entering search terms. It will then follow the criteria you have selected (e.g. country or subject area).

    If you have not selected any criteria in a given category, the entire category will be searched (e.g. all subject areas or all countries).