<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>98(17)</volume><submitter>Wellesen K</submitter><pubmed_abstract>We describe lacerata (lcr) mutants of Arabidopsis, which display various developmental abnormalities, including postgenital organ fusions, and report cloning of the LCR gene by using the maize transposon Enhancer/Suppressor-mutator (En/Spm). The pleiotropic mutant phenotype could be rescued by genetic complementation of lcr mutants with the wild-type LCR gene. The LCR gene encodes a cytochrome P450 monooxygenase, CYP86A8, which catalyzes omega-hydroxylation of fatty acids ranging from C12 to C18:1, as demonstrated by expression of the gene in yeast. Although palmitic and oleic acids were efficient substrates for LCR, 9,10-epoxystearate was not metabolized. Taken together with previous studies, our findings indicate that LCR-dependent omega-hydroxylation of fatty acids could be implicated i</pubmed_abstract><journal>Proceedings of the National Academy of Sciences of the United States of America</journal><pagination>9694-9</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC55514</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Functional analysis of the LACERATA gene of Arabidopsis provides evidence for different roles of fatty acid omega -hydroxylation in development.</pubmed_title><pmcid>PMC55514</pmcid><pubmed_authors>Pinot F</pubmed_authors><pubmed_authors>Nettesheim K</pubmed_authors><pubmed_authors>Wisman E</pubmed_authors><pubmed_authors>Wellesen K</pubmed_authors><pubmed_authors>Durst F</pubmed_authors><pubmed_authors>Benveniste I</pubmed_authors><pubmed_authors>Yephremov A</pubmed_authors><pubmed_authors>Saedler H</pubmed_authors><pubmed_authors>Steiner-Lange S</pubmed_authors></additional><is_claimable>false</is_claimable><name>Functional analysis of the LACERATA gene of Arabidopsis provides evidence for different roles of fatty acid omega -hydroxylation in development.</name><description>We describe lacerata (lcr) mutants of Arabidopsis, which display various developmental abnormalities, including postgenital organ fusions, and report cloning of the LCR gene by using the maize transposon Enhancer/Suppressor-mutator (En/Spm). The pleiotropic mutant phenotype could be rescued by genetic complementation of lcr mutants with the wild-type LCR gene. The LCR gene encodes a cytochrome P450 monooxygenase, CYP86A8, which catalyzes omega-hydroxylation of fatty acids ranging from C12 to C18:1, as demonstrated by expression of the gene in yeast. Although palmitic and oleic acids were efficient substrates for LCR, 9,10-epoxystearate was not metabolized. Taken together with previous studies, our findings indicate that LCR-dependent omega-hydroxylation of fatty acids could be implicated i</description><dates><release>2001-01-01T00:00:00Z</release><publication>2001 Aug</publication><modification>2025-04-26T18:11:47.224Z</modification><creation>2019-03-27T00:12:40Z</creation></dates><accession>S-EPMC55514</accession><cross_references><pubmed>11493698</pubmed><doi>10.1073/pnas.171285998</doi></cross_references></HashMap>