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A protein-specific priority code in presequences determines the efficiency of mitochondrial protein import

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00209805%3A_____%2F25%3A00080362" target="_blank" >RIV/00209805:_____/25:00080362 - isvavai.cz</a>

  • Result on the web

    <a href="https://journals.plos.org/plosbiology/article?id=10.1371/journal.pbio.3003298" target="_blank" >https://journals.plos.org/plosbiology/article?id=10.1371/journal.pbio.3003298</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1371/journal.pbio.3003298" target="_blank" >10.1371/journal.pbio.3003298</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    A protein-specific priority code in presequences determines the efficiency of mitochondrial protein import

  • Original language description

    The biogenesis of mitochondria relies on the import of hundreds of different precursor proteins from the cytosol. Most of these proteins are synthesized with N-terminal presequences which serve as mitochondrial targeting signals. Presequences consistently form amphipathic helices, but they considerably differ with respect to their primary structure and length. Here we show that presequences can be classified into seven different groups based on their specific features. Using a test set of different presequences, we observed that group A presequences endow precursor proteins with improved in vitro import characteristics. We developed IQ-Compete (for Import and de-Quenching Competition assay), a novel assay based on fluorescence de-quenching, to monitor the import efficiencies of mitochondrial precursors in vivo. With this assay, we confirmed the increased import competence of group A presequences. Using mass spectrometry, we found that the presequence of the group A protein Oxa1 specifically recruits the tetratricopeptide repeat (TPR)-containing protein TOMM34 to the cytosolic precursor protein. TOMM34, and the structurally related yeast co-chaperone Cns1, apparently serve as a presequence-specific targeting factor which increases the import efficiency of a specific subset of mitochondrial precursor proteins. Our results suggest that presequences contain a protein-specific priority code that encrypts the targeting mechanism of individual mitochondrial precursor proteins.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10608 - Biochemistry and molecular biology

Result continuities

  • Project

    Result was created during the realization of more than one project. More information in the Projects tab.

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2025

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    PLoS biology

  • ISSN

    1544-9173

  • e-ISSN

    1545-7885

  • Volume of the periodical

    23

  • Issue of the periodical within the volume

    7

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    29

  • Pages from-to

    "e3003298"

  • UT code for WoS article

    001580941900001

  • EID of the result in the Scopus database

    2-s2.0-105011094678