<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Delay C</submitter><funding>Australian Research Council</funding><pagination>4763-4774</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC6760281</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>70(18)</volume><pubmed_abstract>CEPs (C-TERMINALLY ENCODED PEPTIDEs) inhibit Arabidopsis primary root growth by unknown mechanisms. We investigated how CEP3 levels control primary root growth. CEP3 peptide application decreased cell division, S-phase cell number, root meristematic cell number, and meristem zone (MZ) size in a dose- and CEP RECEPTOR1-dependent manner. Grafting showed that CEP3-dependent growth inhibition requires root and shoot CEPR1. CEP3 induced mitotic quiescence in MZ cells significantly faster than that induced by nutrient limitation alone. CEP3 also inhibited the restoration of S-phase to mitotically quiescence cells by nutrient resupply without quantitatively reducing TARGET OF RAPAMYCIN (TOR) kinase activity. In contrast, cep3-1 had an increased meristem size and S-phase cell number under nitrogen</pubmed_abstract><journal>Journal of experimental botany</journal><pubmed_title>CEP3 levels affect starvation-related growth responses of the primary root.</pubmed_title><pmcid>PMC6760281</pmcid><funding_grant_id>DP150104250</funding_grant_id><pubmed_authors>Xiong Y</pubmed_authors><pubmed_authors>Djordjevic MA</pubmed_authors><pubmed_authors>Imin N</pubmed_authors><pubmed_authors>Delay C</pubmed_authors><pubmed_authors>Wang Y</pubmed_authors><pubmed_authors>Tyagi S</pubmed_authors><pubmed_authors>Chapman K</pubmed_authors><pubmed_authors>Taleski M</pubmed_authors></additional><is_claimable>false</is_claimable><name>CEP3 levels affect starvation-related growth responses of the primary root.</name><description>CEPs (C-TERMINALLY ENCODED PEPTIDEs) inhibit Arabidopsis primary root growth by unknown mechanisms. We investigated how CEP3 levels control primary root growth. CEP3 peptide application decreased cell division, S-phase cell number, root meristematic cell number, and meristem zone (MZ) size in a dose- and CEP RECEPTOR1-dependent manner. Grafting showed that CEP3-dependent growth inhibition requires root and shoot CEPR1. CEP3 induced mitotic quiescence in MZ cells significantly faster than that induced by nutrient limitation alone. CEP3 also inhibited the restoration of S-phase to mitotically quiescence cells by nutrient resupply without quantitatively reducing TARGET OF RAPAMYCIN (TOR) kinase activity. In contrast, cep3-1 had an increased meristem size and S-phase cell number under nitrogen</description><dates><release>2019-01-01T00:00:00Z</release><publication>2019 Sep</publication><modification>2025-04-04T07:10:43.719Z</modification><creation>2019-10-11T07:10:53Z</creation></dates><accession>S-EPMC6760281</accession><cross_references><pubmed>31173100</pubmed><doi>10.1093/jxb/erz270</doi></cross_references></HashMap>