Mitochondrial matrix protein LETMD1 maintains thermogenic capacity of brown adipose tissue in male mice

Cited 12 time in scopus
Metadata Downloads

Full metadata record

DC FieldValueLanguage
dc.contributor.authorAnna Park-
dc.contributor.authorK E Kim-
dc.contributor.authorI Park-
dc.contributor.authorS H Lee-
dc.contributor.authorK Y {Park-
dc.contributor.authorM Jung-
dc.contributor.authorx Li-
dc.contributor.authorM B Sleiman-
dc.contributor.authorSu Jeong Lee-
dc.contributor.authorDae Soo Kim-
dc.contributor.authorJ Kim-
dc.contributor.authorD S Lim-
dc.contributor.authorEui-Jeon Woo-
dc.contributor.authorEun-Woo Lee-
dc.contributor.authorBaek Soo Han-
dc.contributor.authorKyoung-Jin Oh-
dc.contributor.authorSang Chul Lee-
dc.contributor.authorJ Auwerx-
dc.contributor.authorJ Y Mun-
dc.contributor.authorH W Rhee-
dc.contributor.authorWon Kon Kim-
dc.contributor.authorKwang-Hee Bae-
dc.contributor.authorJ M Suh-
dc.date.accessioned2023-06-26T16:32:31Z-
dc.date.available2023-06-26T16:32:31Z-
dc.date.issued2023-
dc.identifier.issn2041-1723-
dc.identifier.urihttps://oak.kribb.re.kr/handle/201005/32170-
dc.description.abstractBrown adipose tissue (BAT) has abundant mitochondria with the unique capability of generating heat via uncoupled respiration. Mitochondrial uncoupling protein 1 (UCP1) is activated in BAT during cold stress and dissipates mitochondrial proton motive force generated by the electron transport chain to generate heat. However, other mitochondrial factors required for brown adipocyte respiration and thermogenesis under cold stress are largely unknown. Here, we show LETM1 domain-containing protein 1 (LETMD1) is a BAT-enriched and cold-induced protein required for cold-stimulated respiration and thermogenesis of BAT. Proximity labeling studies reveal that LETMD1 is a mitochondrial matrix protein. Letmd1 knockout male mice display aberrant BAT mitochondria and fail to carry out adaptive thermogenesis under cold stress. Letmd1 knockout BAT is deficient in oxidative phosphorylation (OXPHOS) complex proteins and has impaired mitochondrial respiration. In addition, BAT-specific Letmd1 deficient mice exhibit phenotypes identical to those observed in Letmd1 knockout mice. Collectively, we demonstrate that the BAT-enriched mitochondrial matrix protein LETMD1 plays a tissue-autonomous role that is essential for BAT mitochondrial function and thermogenesis.-
dc.publisherSpringer-Nature Pub Group-
dc.titleMitochondrial matrix protein LETMD1 maintains thermogenic capacity of brown adipose tissue in male mice-
dc.title.alternativeMitochondrial matrix protein LETMD1 maintains thermogenic capacity of brown adipose tissue in male mice-
dc.typeArticle-
dc.citation.titleNature Communications-
dc.citation.number0-
dc.citation.endPage3746-
dc.citation.startPage3746-
dc.citation.volume14-
dc.contributor.affiliatedAuthorAnna Park-
dc.contributor.affiliatedAuthorSu Jeong Lee-
dc.contributor.affiliatedAuthorDae Soo Kim-
dc.contributor.affiliatedAuthorEui-Jeon Woo-
dc.contributor.affiliatedAuthorEun-Woo Lee-
dc.contributor.affiliatedAuthorBaek Soo Han-
dc.contributor.affiliatedAuthorKyoung-Jin Oh-
dc.contributor.affiliatedAuthorSang Chul Lee-
dc.contributor.affiliatedAuthorWon Kon Kim-
dc.contributor.affiliatedAuthorKwang-Hee Bae-
dc.contributor.alternativeName박안나-
dc.contributor.alternativeName김광은-
dc.contributor.alternativeName박이삭-
dc.contributor.alternativeName이상헌-
dc.contributor.alternativeName박건영-
dc.contributor.alternativeName정민교-
dc.contributor.alternativeNameLi-
dc.contributor.alternativeNameSleiman-
dc.contributor.alternativeName이수정-
dc.contributor.alternativeName김대수-
dc.contributor.alternativeName김재훈-
dc.contributor.alternativeName임대식-
dc.contributor.alternativeName우의전-
dc.contributor.alternativeName이은우-
dc.contributor.alternativeName한백수-
dc.contributor.alternativeName오경진-
dc.contributor.alternativeName이상철-
dc.contributor.alternativeNameAuwerx-
dc.contributor.alternativeName문지영-
dc.contributor.alternativeName이현우-
dc.contributor.alternativeName김원곤-
dc.contributor.alternativeName배광희-
dc.contributor.alternativeName서재명-
dc.identifier.bibliographicCitationNature Communications, vol. 14, pp. 3746-3746-
dc.identifier.doi10.1038/s41467-023-39106-z-
dc.description.journalClassY-
Appears in Collections:
Division of A.I. & Biomedical Research > Digital Biotech Innovation Center > 1. Journal Articles
Synthetic Biology and Bioengineering Research Institute > Genome Editing Research Center > 1. Journal Articles
Division of A.I. & Biomedical Research > Metabolic Regulation Research Center > 1. Journal Articles
Division of Research on National Challenges > Biodefense Research Center > 1. Journal Articles
Files in This Item:
  • There are no files associated with this item.


Items in OpenAccess@KRIBB are protected by copyright, with all rights reserved, unless otherwise indicated.