<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Yoshinari A</submitter><funding>Ministry of Education, Culture, Sports, Science, and Technology of Japan</funding><funding>Japanese Society for the Promotion of Science (JSPS</funding><pagination>420-438</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC8136889</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>33(2)</volume><pubmed_abstract>Plants take up and translocate nutrients through transporters. In Arabidopsis thaliana, the borate exporter BOR1 acts as a key transporter under boron (B) limitation in the soil. Upon sufficient-B supply, BOR1 undergoes ubiquitination and is transported to the vacuole for degradation, to avoid overaccumulation of B. However, the mechanisms underlying B-sensing and ubiquitination of BOR1 are unknown. In this study, we confirmed the lysine-590 residue in the C-terminal cytosolic region of BOR1 as the direct ubiquitination site and showed that BOR1 undergoes K63-linked polyubiquitination. A forward genetic screen identified that amino acid residues located in vicinity of the substrate-binding pocket of BOR1 are essential for the vacuolar sorting. BOR1 variants that lack B-transport activity showed a significant reduction of polyubiquitination and subsequent vacuolar sorting. Coexpression of wild-type (WT) and a transport-defective variant of BOR1 in the same cells showed degradation of the WT but not the variant upon sufficient-B supply. These findings suggest that polyubiquitination of BOR1 relies on its conformational transition during the transport cycle. We propose a model in which BOR1, as a B transceptor, directly senses the B concentration and promotes its own polyubiquitination and vacuolar sorting for quick and precise maintenance of B homeostasis.</pubmed_abstract><journal>The Plant cell</journal><pubmed_title>Transport-coupled ubiquitination of the borate transporter BOR1 for its boron-dependent degradation.</pubmed_title><pmcid>PMC8136889</pmcid><funding_grant_id>19H05637</funding_grant_id><funding_grant_id>19K16164</funding_grant_id><funding_grant_id>19H05763</funding_grant_id><funding_grant_id>26712007</funding_grant_id><funding_grant_id>252799</funding_grant_id><pubmed_authors>Ogino Y</pubmed_authors><pubmed_authors>Beier MP</pubmed_authors><pubmed_authors>Hosokawa T</pubmed_authors><pubmed_authors>Yoshinari A</pubmed_authors><pubmed_authors>Oshima K</pubmed_authors><pubmed_authors>Takasuka TE</pubmed_authors><pubmed_authors>Fujiwara T</pubmed_authors><pubmed_authors>Takano J</pubmed_authors><pubmed_authors>Hori C</pubmed_authors><pubmed_authors>Fukao Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Transport-coupled ubiquitination of the borate transporter BOR1 for its boron-dependent degradation.</name><description>Plants take up and translocate nutrients through transporters. In Arabidopsis thaliana, the borate exporter BOR1 acts as a key transporter under boron (B) limitation in the soil. Upon sufficient-B supply, BOR1 undergoes ubiquitination and is transported to the vacuole for degradation, to avoid overaccumulation of B. However, the mechanisms underlying B-sensing and ubiquitination of BOR1 are unknown. In this study, we confirmed the lysine-590 residue in the C-terminal cytosolic region of BOR1 as the direct ubiquitination site and showed that BOR1 undergoes K63-linked polyubiquitination. A forward genetic screen identified that amino acid residues located in vicinity of the substrate-binding pocket of BOR1 are essential for the vacuolar sorting. BOR1 variants that lack B-transport activity showed a significant reduction of polyubiquitination and subsequent vacuolar sorting. Coexpression of wild-type (WT) and a transport-defective variant of BOR1 in the same cells showed degradation of the WT but not the variant upon sufficient-B supply. These findings suggest that polyubiquitination of BOR1 relies on its conformational transition during the transport cycle. We propose a model in which BOR1, as a B transceptor, directly senses the B concentration and promotes its own polyubiquitination and vacuolar sorting for quick and precise maintenance of B homeostasis.</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Apr</publication><modification>2024-11-08T11:36:42.464Z</modification><creation>2022-02-11T13:05:10.749Z</creation></dates><accession>S-EPMC8136889</accession><cross_references><pubmed>33866370</pubmed><doi>10.1093/plcell/koaa020</doi></cross_references></HashMap>