Evidence map›Paper›PMID 7862636›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1995

The canine betaine gamma-amino-n-butyric acid transporter gene: diverse mRNA isoforms are regulated by hypertonicity and are expressed in a tissue-specific manner.

M Takenaka, S M Bagnasco, A S Preston, S Uchida, A Yamauchi, H M Kwon, J S Handler

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1995. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
6.6field-weighted citation impact, top 3% 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

9 citing papers in PubMed, 60 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. Downregulation of the creatine transporter SLC6A8 by JAK2.The Journal of membrane biology · 2012
    Article
  5. Article
  6. Article
  7. Article
  8. Characterization of the osmotic response element of the human aldose reductase gene promoter.Proceedings of the National Academy of Sciences of the United States of America · 1996
    Article
  9. 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

7 authors at 2 institutions in 1 country.

M TakenakaDepartment of Medicine, Johns Hopkins University School of Medicine, Baltimore, MD 21205.
S M Bagnasco
A S Preston
S Uchida
A Yamauchi
H M Kwon
J S Handler
Johns Hopkins Medicine · USJohns Hopkins University · US

Funding

STRUCTURE AND FUNCTION STUDIES OF CLONED SODIUM AND HYDROGEN EXCHANGERSP01DK044484 · NIDDK · JOHNS HOPKINS UNIVERSITY · PI DONOWITZ, MARK · 1992 to 2002
$2.6M
NIDDK NIH HHS 1PO1 DK-44484
6 · The paper itself

Abstract

The Na(+)- and Cl(-)-coupled betaine transporter, designated BGT1, a member of the neurotransmitter transporter gene family, is responsible for accumulation of betaine in hypertonic Madin-Darby canine kidney (MDCK) cells and presumably in the hypertonic renal medulla. The canine gene for the betaine gamma-amino-n-butyric acid transporter has been cloned and analyzed. The gene extends over 28 kb and consists of 18 exons. The 5' end of the gene has three alternative first exons (1A, 1B, and 1C+D). Analysis of BGT1 mRNA revealed that there is considerable divergence in the 5' untranslated sequence resulting from three different 5' end motifs (A, B, and C) followed by an alternative motif (D) as well as two internal acceptor sites for splicing. Eight kinds of BGT1 mRNA were classified into three types (A, B, and C) according to the 5' end sequence. Northern blot analysis using probes specific for the A, B, or C motif revealed that hypertonicity induces all three types in MDCK cells. Reverse transcription and polymerase chain reaction showed that each type was expressed in a tissue-specific manner. Primer extension and/or RNase protection assays as well as transfection assays into MDCK cells demonstrated that exons 1A, 1B, and 1C+D have independent transcription initiation sites under control of independent promoters. Diverse mRNA isoforms are regulated by hypertonicity and are expressed in a tissue-specific manner.

Indexed as

Membrane Transport ProteinsOrganic Anion TransportersAnimalsBase SequenceCarrier ProteinsCell LineDNADogsExonsGABA Plasma Membrane Transport ProteinsIntronsMembrane ProteinsMolecular Sequence DataOsmolar ConcentrationPromoter Regions, GeneticRNA, Messengerbetaine plasma membrane transport proteinsCarrier ProteinsDNAGABA Plasma Membrane Transport ProteinsMembrane ProteinsMembrane Transport ProteinsOrganic Anion TransportersRNA, Messenger

Identifiers

PMID7862636
PMCPMC42639
OpenAlexW1988727187

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.