Evidence map›Paper›PMID 27252523›Full record

ArticleJournal of lipid research2016

E4BP4 is an insulin-induced stabilizer of nuclear SREBP-1c and promotes SREBP-1c-mediated lipogenesis.

Xin Tong, Pei Li, Deqiang Zhang, Kyle VanDommelen, Neil Gupta, Liangyou Rui, M Bishr Omary, Lei Yin

Open access · hybridAbstract read
In one paragraph

Article in Journal of lipid research, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.6field-weighted citation impact, top 17% of its field
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

14 citing papers in PubMed, 25 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. A new border for circadian rhythm gene NFIL3 in diverse fields of cancer.Clinical & translational oncology : official publication of the Federation of Spanish Oncology Societies and of the National Cancer Institute of Mexico · 2023
    Review
  6. Preventive nutrition and food science · 2022
    Article
  7. Review
  8. Hepatic metabolic regulation by nuclear factor E4BP4.Journal of molecular endocrinology · 2021
    Review
  9. Hepatic E4BP4 induction promotes lipid accumulation by suppressing AMPK signaling in response to chemical or diet-induced ER stress.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2020
    Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
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

8 authors at 2 institutions in 2 countries.

Xin TongDepartment of Molecular and Integrative Physiology, University of Michigan Medical School, Ann Arbor, MI 48019.
Pei LiXiangya School of Medicine, Central South University, Changsha 410013, People's Republic of China.
Deqiang ZhangDepartment of Molecular and Integrative Physiology, University of Michigan Medical School, Ann Arbor, MI 48019.
Kyle VanDommelenDepartment of Molecular and Integrative Physiology, University of Michigan Medical School, Ann Arbor, MI 48019.
Neil GuptaDepartment of Molecular and Integrative Physiology, University of Michigan Medical School, Ann Arbor, MI 48019.
Liangyou RuiDepartment of Molecular and Integrative Physiology, University of Michigan Medical School, Ann Arbor, MI 48019.
M Bishr OmaryDepartment of Molecular and Integrative Physiology, University of Michigan Medical School, Ann Arbor, MI 48019.
Lei YinDepartment of Molecular and Integrative Physiology, University of Michigan Medical School, Ann Arbor, MI 48019 leiyin@umich.edu.
University of Michigan–Ann Arbor · USCentral South University · CN

Funding

PUBLIC HEALTH DEMONSTRATIONP60DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MYERS, MARTIN G · 1985 to 2012
$26.5M
Regional Pilot And Feasibility Study Grants ProgramP30DK020572 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI Scott Soleimanpour · 2013 to 2026
$24.3M
University of Michigan Center for Gastrointestinal ResearchP30DK034933 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI OWYANG, CHUNG · 1986 to 2021
$22.5M
Keratin Biology and Disease Aspects in Simple EpitheliaR01DK047918 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI OMARY, BISHR · 1995 to 2018
$6.6M
Significance and mechanisms of hepatic ChREBPα induction via post-translational modifications in diet-induced NASHR01DK099593 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI YIN, LEI · 2014 to 2025
$4.5M
Interfacing computation and engineering with digestive and metabolic physiologyR25DK088752 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI MACDOUGALD, ORMOND A · 2010 to 2020
$1.1M
Biology of nuclear receptor Rev-erb alpha in circadian rhythm and metabolismR00DK077449 · NIDDK · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI YIN, LEI · 2009 to 2011
$724k
Biology of nuclear receptor rev-erb alpha in circadian rhythm and metabolismK99DK077449 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI YIN, LEI · 2007 to 2009
$146k
NIDDK NIH HHS K99 DK077449NIDDK NIH HHS P30 DK020572NIDDK NIH HHS P30 DK034933NIDDK NIH HHS P60 DK020572NIDDK NIH HHS R00 DK077449NIDDK NIH HHS R01 DK047918NIDDK NIH HHS R01 DK099593NIDDK NIH HHS R25 DK088752
6 · The paper itself

Abstract

Upon food intake, insulin stimulates de novo lipogenesis (DNL) in hepatocytes via the AKT-mTORC1-sterol regulatory element-binding protein (SREBP)-1c pathway. How insulin maintains the maximal SREBP-1c activities during the entire feeding state remains elusive. We previously reported that insulin induced b-ZIP transcription factor, E4-binding protein 4 (E4BP4), in hepatocytes. In the current study, we show that insulin injection increases hepatic E4bp4 expression by activating the AKT-mTORC1-SREBP-1c pathway in hepatocytes. E4bp4-deficient hepatocytes not only fail to maintain robust DNL but also become resistant to SREBP-1c-induced lipogenesis. In vivo, acute depletion of E4bp4 in the liver by adenoviral shRNA reduces the expression of lipogenic enzymes and results in reduced levels of serum triglycerides and cholesterol during the postprandial phase. In hepatocytes, E4BP4 interacts with nuclear SREBP-1c to preserve its acetylation, and subsequently protects it from ubiquitination-dependent degradation. In conclusion, the current studies uncover a novel positive feedback pathway mediated by E4BP4 to augment SREBP-1c-mediated DNL in the liver during the fed state.

Indexed as

Transcription, GeneticAnimalsAppetite RegulationBasic-Leucine Zipper Transcription FactorsFatty AcidsFatty LiverGene Expression RegulationHepatocytesHumansInsulinLipogenesisLiverMicePostprandial PeriodProteolysisSterol Regulatory Element Binding Protein 1Basic-Leucine Zipper Transcription FactorsFatty AcidsInsulinNfil3 protein, mouseSterol Regulatory Element Binding Protein 1Triglyceridesacetylationde novo lipogenesisE4-binding protein 4fatty acid synthesisinsulin signalinglipidsliverpost-prandialsterol regulatory element-binding protein 1ctranscriptiontriglyceridesubiquitination

Identifiers

PMID27252523
PMCPMC4918851
OpenAlexW2416783410

What OpenQuestion holds

Textmetadata
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.