<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Allen MD</submitter><funding>NIGMS NIH HHS</funding><pagination>1841-52</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC2043389</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>6(10)</volume><pubmed_abstract>Previously, we had identified FOX1 and FTR1 as iron deficiency-inducible components of a high-affinity copper-dependent iron uptake pathway in Chlamydomonas. In this work, we survey the version 3.0 draft genome to identify a ferrireductase, FRE1, and two ZIP family proteins, IRT1 and IRT2, as candidate ferrous transporters based on their increased expression in iron-deficient versus iron-replete cells. In a parallel proteomic approach, we identified FEA1 and FEA2 as the major proteins secreted by iron-deficient Chlamydomonas reinhardtii. The recovery of FEA1 and FEA2 from the medium of Chlamydomonas strain CC425 cultures is strictly correlated with iron nutrition status, and the accumulation of the corresponding mRNAs parallels that of the Chlamydomonas FOX1 and FTR1 mRNAs, although the ma</pubmed_abstract><journal>Eukaryotic cell</journal><pubmed_title>FEA1, FEA2, and FRE1, encoding two homologous secreted proteins and a candidate ferrireductase, are expressed coordinately with FOX1 and FTR1 in iron-deficient Chlamydomonas reinhardtii.</pubmed_title><pmcid>PMC2043389</pmcid><funding_grant_id>R01 GM042143</funding_grant_id><funding_grant_id>T32 GM007185</funding_grant_id><funding_grant_id>R37 GM042143</funding_grant_id><funding_grant_id>GM077066</funding_grant_id><funding_grant_id>GM07185</funding_grant_id><funding_grant_id>F31 GM077066</funding_grant_id><funding_grant_id>GM42143</funding_grant_id><pubmed_authors>Kropat J</pubmed_authors><pubmed_authors>Allen MD</pubmed_authors><pubmed_authors>Merchant SS</pubmed_authors><pubmed_authors>del Campo JA</pubmed_authors></additional><is_claimable>false</is_claimable><name>FEA1, FEA2, and FRE1, encoding two homologous secreted proteins and a candidate ferrireductase, are expressed coordinately with FOX1 and FTR1 in iron-deficient Chlamydomonas reinhardtii.</name><description>Previously, we had identified FOX1 and FTR1 as iron deficiency-inducible components of a high-affinity copper-dependent iron uptake pathway in Chlamydomonas. In this work, we survey the version 3.0 draft genome to identify a ferrireductase, FRE1, and two ZIP family proteins, IRT1 and IRT2, as candidate ferrous transporters based on their increased expression in iron-deficient versus iron-replete cells. In a parallel proteomic approach, we identified FEA1 and FEA2 as the major proteins secreted by iron-deficient Chlamydomonas reinhardtii. The recovery of FEA1 and FEA2 from the medium of Chlamydomonas strain CC425 cultures is strictly correlated with iron nutrition status, and the accumulation of the corresponding mRNAs parallels that of the Chlamydomonas FOX1 and FTR1 mRNAs, although the ma</description><dates><release>2007-01-01T00:00:00Z</release><publication>2007 Oct</publication><modification>2025-06-01T01:12:15.558Z</modification><creation>2019-03-27T02:21:49Z</creation></dates><accession>S-EPMC2043389</accession><cross_references><pubmed>17660359</pubmed><doi>10.1128/ec.00205-07</doi><doi>10.1128/EC.00205-07</doi></cross_references></HashMap>