Evidence map›Paper›PMID 26637528›Full record

ArticleGenes & development2015

SREBP and MDT-15 protect C. elegans from glucose-induced accelerated aging by preventing accumulation of saturated fat.

Dongyeop Lee, Dae-Eun Jeong, Heehwa G Son, Yasuyo Yamaoka, Hyunmin Kim, Keunhee Seo, Abdul Aziz Khan, Tae-Young Roh, Dae Won Moon, Youngsook Lee and 1 more

Open access · diamondAbstract read
In one paragraph

Article in Genes & development, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 75 papers.

0numbers the graph read from it
0cells of the map it votes in
75citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

75 citing papers in PubMed, 133 citations in OpenAlex.

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15 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 2 institutions in 1 country.

Dongyeop LeeDepartment of Life Sciences, Pohang University of Science and Technology, Pohang, Gyeongbuk 37673, South Korea;
Dae-Eun JeongDepartment of Life Sciences, Pohang University of Science and Technology, Pohang, Gyeongbuk 37673, South Korea;
Heehwa G SonDepartment of Life Sciences, Pohang University of Science and Technology, Pohang, Gyeongbuk 37673, South Korea;
Yasuyo YamaokaDepartment of Life Sciences, Pohang University of Science and Technology, Pohang, Gyeongbuk 37673, South Korea;
Hyunmin KimDepartment of New Biology, Daegu Gyeongbuk Institute of Science and Technology, Daegu 42988, South Korea;
Keunhee SeoDepartment of Life Sciences, Pohang University of Science and Technology, Pohang, Gyeongbuk 37673, South Korea;
Abdul Aziz KhanDivision of Integrative Biosciences and Biotechnology, Pohang University of Science and Technology, Pohang, Gyeongbuk 37673, South Korea;
Tae-Young RohDepartment of Life Sciences, Pohang University of Science and Technology, Pohang, Gyeongbuk 37673, South Korea; Division of Integrative Biosciences and Biotechnology, Pohang University of Science and Technology, Pohang, Gyeongbuk 37673, South Korea;
Dae Won MoonDepartment of New Biology, Daegu Gyeongbuk Institute of Science and Technology, Daegu 42988, South Korea;
Youngsook LeeDepartment of Life Sciences, Pohang University of Science and Technology, Pohang, Gyeongbuk 37673, South Korea; Division of Integrative Biosciences and Biotechnology, Pohang University of Science and Technology, Pohang, Gyeongbuk 37673, South Korea;
Seung-Jae V LeeDepartment of Life Sciences, Pohang University of Science and Technology, Pohang, Gyeongbuk 37673, South Korea; Information Technology Convergence Engineering, Pohang University of Science and Technology, Pohang, Gyeongbuk 37673, South Korea; School of Interdisciplinary Bioscience and Bioengineering, Pohang University of Science and Technology, Pohang, Gyeongbuk 37673, South Korea.
Pohang University of Science and Technology · KRDaegu Gyeongbuk Institute of Science and Technology · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Glucose-rich diets shorten the life spans of various organisms. However, the metabolic processes involved in this phenomenon remain unknown. Here, we show that sterol regulatory element-binding protein (SREBP) and mediator-15 (MDT-15) prevent the life-shortening effects of a glucose-rich diet by regulating fat-converting processes in Caenorhabditis elegans. Up-regulation of the SREBP/MDT-15 transcription factor complex was necessary and sufficient for alleviating the life-shortening effect of a glucose-rich diet. Glucose feeding induced key enzymes that convert saturated fatty acids (SFAs) to unsaturated fatty acids (UFAs), which are regulated by SREBP and MDT-15. Furthermore, SREBP/MDT-15 reduced the levels of SFAs and moderated glucose toxicity on life span. Our study may help to develop strategies against elevated blood glucose and free fatty acids, which cause glucolipotoxicity in diabetic patients.

Indexed as

AgingAnimalsCaenorhabditis elegansCaenorhabditis elegans ProteinsDietDietary SucroseEnzyme InductionFatty Acid DesaturasesFatty AcidsGene Expression Regulation, DevelopmentalGenome-Wide Association StudyGlucoseRNA InterferenceSterol Regulatory Element Binding ProteinsTranscription FactorsCaenorhabditis elegans ProteinsDietary SucroseFatty Acid DesaturasesFatty AcidsGlucoseMDT-15 protein, C elegansSterol Regulatory Element Binding ProteinsTranscription FactorsagingC. elegansfatglucoseMDT-15SREBP

Identifiers

PMID26637528
PMCPMC4691952
OpenAlexW2189389315

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.