<oai_dc:dc xmlns:dc="http://purl.org/dc/elements/1.1/" xmlns:oai_dc="http://www.openarchives.org/OAI/2.0/oai_dc/" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.openarchives.org/OAI/2.0/oai_dc/ http://www.openarchives.org/OAI/2.0/oai_dc.xsd">
  <dc:creator>Finger, Yannik</dc:creator>
  <dc:creator>Habich, Markus</dc:creator>
  <dc:creator>Gerlich, Sarah</dc:creator>
  <dc:creator>Urbanczyk, Sophia</dc:creator>
  <dc:creator>Logt, Erik</dc:creator>
  <dc:creator>Koch, Julian</dc:creator>
  <dc:creator>Schu, Laura</dc:creator>
  <dc:creator>Lapacz, Kim Jasmin</dc:creator>
  <dc:creator>Ali, Muna</dc:creator>
  <dc:creator>Petrungaro, Carmelina</dc:creator>
  <dc:creator>Salscheider, Silja Lucia</dc:creator>
  <dc:creator>Pichlo, Christian</dc:creator>
  <dc:creator>Baumann, Ulrich</dc:creator>
  <dc:creator>Mielenz, Dirk</dc:creator>
  <dc:creator>Dengjel, Jörn</dc:creator>
  <dc:creator>Brachvogel, Bent</dc:creator>
  <dc:creator>Hofmann, Kay</dc:creator>
  <dc:creator>Riemer, Jan</dc:creator>
  <dc:date>2020-08-20</dc:date>
  <dc:description xmlns:ns0="xml" ns0:lang="en">Plasticity of the proteome is critical to adapt to varying conditions. Control of  mitochondrial protein import contributes to this plasticity. Here, we identified a pathway  that regulates mitochondrial protein import by regulated N-terminal processing. We  demonstrate that dipeptidyl peptidases 8/9 (DPP8/9) mediate the N-terminal  processing of adenylate kinase 2 (AK2) en route to mitochondria. We show that AK2  is a substrate of the mitochondrial disulfide relay, thus lacking an N-terminal  mitochondrial targeting sequence and undergoing comparatively slow import. DPP9-  mediated processing of AK2 induces its rapid proteasomal degradation and prevents  cytosolic accumulation of enzymatically active AK2. Besides AK2, we identify more  than 100 mitochondrial proteins with putative DPP8/9 recognition sites and  demonstrate that DPP8/9 influence the cellular levels of a number of these proteins.  Collectively, we provide in this study a conceptual framework on how regulated  cytosolic processing controls levels of mitochondrial proteins as well as their dual  localization to mitochondria and other compartments.</dc:description>
  <dc:format>application/pdf</dc:format>
  <dc:identifier>https://folia.unifr.ch/global/documents/308905</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/308905/files/den_pdi.pdf</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/308905/files/den_pdi_sm.pdf</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/308905/files/descr.txt</dc:identifier>
  <dc:identifier>https://folia.unifr.ch/documents/308905/files/MPX_MYPX.txt</dc:identifier>
  <dc:language>eng</dc:language>
  <dc:relation>info:eu-repo/semantics/altIdentifier/doi/10.15252/embj.2019103889</dc:relation>
  <dc:rights>info:eu-repo/semantics/openAccess</dc:rights>
  <dc:rights>License undefined</dc:rights>
  <dc:source>The EMBO Journal. - 2020, vol. 39, no. 19, p. e103889</dc:source>
  <dc:subject>info:eu-repo/classification/udc/57</dc:subject>
  <dc:title xmlns:ns1="xml" ns1:lang="en">Proteasomal degradation induced by DPP9-mediated processing competes with mitochondrial protein import</dc:title>
  <dc:type>http://purl.org/coar/resource_type/c_6501</dc:type>
</oai_dc:dc>
