Evidence map›Paper›PMID 22526585›Full record

ArticleDigestive diseases and sciences2012

PER1 modulates SGLT1 transcription in vitro independent of E-box status.

Anita Balakrishnan, Adam T Stearns, Stanley W Ashley, David B Rhoads, Ali Tavakkolizadeh

Abstract readComparative Study
In one paragraph

Article in Digestive diseases and sciences, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.5field-weighted citation impact, top 43% 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

13 citing papers in PubMed, 17 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Animals : an open access journal from MDPI · 2021
    Article
  5. Circadian clocks in the digestive system.Nature reviews. Gastroenterology & hepatology · 2021
    Review
  6. Glucose transporters in the small intestine in health and disease.Pflugers Archiv : European journal of physiology · 2020
    Review
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
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

5 authors at 3 institutions in 2 countries.

Anita BalakrishnanDepartment of Surgery, Brigham and Women's Hospital, Boston, MA 02115, USA. anita.balakrishnan@doctors.org.uk
Adam T Stearns
Stanley W Ashley
David B Rhoads
Ali Tavakkolizadeh
Brigham and Women's Hospital · USHarvard University · USUniversity of Oxford · GB

Funding

ROLE OF DIETARY CONSTITUENTS ON GENE EXPRESSION IN INTESTINAL EPITHELIUMP30DK040561 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI CHRISTOPHER P DUGGAN · 1994 to 2026
$31.6M
SURGERY AND INTESTINAL ADAPTATIONR01DK047326 · NIDDK · BRIGHAM AND WOMEN'S HOSPITAL · PI ASHLEY, STANLEY W · 1999 to 2005
$983k
NIDDK NIH HHS 5 R01 DK047326NIDDK NIH HHS P30 DK040561NIDDK NIH HHS P30-DK040561NIDDK NIH HHS R01 DK047326
6 · The paper itself

Abstract

BACKGROUND AND

aimsThe intestine demonstrates profound circadian rhythmicity in glucose absorption in rodents, mediated entirely by rhythmicity in the transcription, translation, and function of the sodium glucose co-transporter SGLT1 (Slc5a1). Clock genes are rhythmic in the intestine and have been implicated in the regulation of rhythmicity of other intestinal genes; however, their role in the regulation of SGLT1 is unknown. We investigated the effects of one clock gene, PER1, on SGLT1 transcription in vitro.

methodsCaco-2 cells were stably transfected with knockdown vectors for PER1 and mRNA expression of clock genes and SGLT1 determined using quantitative polymerase chain reaction (qPCR). Chinese hamster ovary (CHO) cells were transiently cotransfected with combinations of the PER1 expression vectors and the wild-type SGLT1-luciferase promoter construct or the promoter with mutated E-box sequences.

resultsKnockdown of PER1 increased native SGLT1 expression in Caco-2 enterocytes, while promoter studies confirmed that the inhibitory activity of PER1 on SGLT1 occurs via the proximal 1 kb of the SGLT1 promoter. E-box sites exerted a suppressive effect on the SGLT1 promoter; however, mutation of E-boxes had little effect on the inhibitory activity of PER1 on the SGLT1 promoter suggesting that the actions of PER1 on SGLT1 are independent of E-boxes.

conclusionsOur findings suggest that PER1 exerts an indirect suppressive effect on SGLT1, possibly acting via other clock-controlled genes binding to non-E-box sites on the SGLT1 promoter. Understanding the regulation of rhythmicity of SGLT1 may lead to new treatments for the modulation of SGLT1 expression in conditions such as malabsorption, diabetes, and obesity.

Indexed as

AnimalsBlotting, WesternCaco-2 CellsCells, CulturedCricetinaeDown-RegulationE-Box ElementsFemaleGene Expression RegulationHumansIn Vitro TechniquesPeriod Circadian ProteinsPromoter Regions, GeneticRNA, MessengerSensitivity and SpecificitySodium-Glucose Transporter 1PER1 protein, humanPeriod Circadian ProteinsRNA, MessengerSodium-Glucose Transporter 1

Identifiers

PMID22526585
PMCPMC3376756
OpenAlexW2047345051

What OpenQuestion holds

Textmetadata
LicenceTDM
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.