Evidence map›Paper›PMID 8421672›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America1993

Phylogenic and ontogenic expression of hepatocellular bile acid transport.

J L Boyer, B Hagenbuch, M Ananthanarayanan, F Suchy, B Stieger, P J Meier

Open access · greenAbstract readComparative Study
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 1993. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.8field-weighted citation impact, top 7% 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

11 citing papers in PubMed, 81 citations in OpenAlex.

  1. Review
  2. Article
  3. Bile acid transporters.Journal of lipid research · 2009
    Review
  4. Article
  5. Expression cloning of two genes that together mediate organic solute and steroid transport in the liver of a marine vertebrate.Proceedings of the National Academy of Sciences of the United States of America · 2001
    Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Expression cloning of a rat liver Na(+)-independent organic anion transporter.Proceedings of the National Academy of Sciences of the United States of America · 1994
    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

6 authors at 1 institution in 1 country.

J L BoyerMt. Desert Island Biological Laboratory, Salsbury Cove, ME 04672.
B Hagenbuch
M Ananthanarayanan
F Suchy
B Stieger
P J Meier
Mount Desert Island Biological Laboratory · US

Funding

Yale Liver CenterP30DK034989 · NIDDK · YALE UNIVERSITY · PI WAJAHAT Zafar MEHAL · 1986 to 2026
$31.1M
MECHANISMS OF BILE SECRETION &CHOLESTASISR37DK025636 · NIDDK · YALE UNIVERSITY · PI BOYER, JAMES LORENZEN · 1990 to 2017
$9.7M
MECHANISMS OF BILE SECRETION AND CHOLESTASISR01DK025636 · NIDDK · YALE UNIVERSITY · PI BOYER, JAMES LORENZEN · 1986 to 2007
$6.1M
ONTOGENY OF HEPATIC ION TRANSPORTR37HD020632 · NICHD · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI SUCHY, FREDERICK J · 1998 to 2007
$3.7M
ONTOGENY OF HEPATIC ION TRANSPORTR01HD020632 · NICHD · YALE UNIVERSITY · PI SUCHY, FREDERICK J · 1985 to 1997
–
NICHD NIH HHS HD20632NIDDK NIH HHS DK25636NIDDK NIH HHS DK34989
6 · The paper itself

Abstract

The phylogenic and ontogenic expression of mRNA for the Na+/bile acid cotransporter was determined by Northern analysis utilizing a full-length cDNA probe recently cloned from rat liver. mRNA was detected in several mammalian species, including rat, mouse, and man, but could not be found in livers from nonmammalian species, including chicken, turtle, frog, and small skate. When expression of the bile acid transporter in developing rat liver was studied, mRNA was detected between 18 and 21 days of gestation, at the time when Na(+)-dependent bile acid transport is first detected. Two hepatoma cell lines (HTC and HepG2), the latter of which is known to have lost the Na+/bile acid cotransport system, also did not express mRNA for this transporter. Finally, when mRNA from the lower vertebrate (the small skate) was injected into Xenopus oocytes, only a sodium-independent, chloride-dependent transport system for bile acids was expressed, confirming the integrity of the mRNA and consistent with prior functional studies of bile acid transport in this species. These findings establish that the Na+/bile acid cotransport mRNA is first transcribed in mammalian species, a process that is recapitulated late during mammalian fetal development in rat liver, and that this mRNA is lost in dedifferentiated hepatocytes. In contrast, the mRNA for a multispecific Na+/independent organic anion transport system is transcribed earlier in vertebrate evolution.

Indexed as

Organic Anion Transporters, Sodium-DependentSymportersAgingAnimalsBiological TransportCarrier ProteinsCell DifferentiationGene ExpressionLiverMammalsPhylogenyRNA, MessengerTaurocholic AcidVertebratesCarrier ProteinsOrganic Anion Transporters, Sodium-DependentRNA, Messengersodium-bile acid cotransporterSymportersTaurocholic Acid

Identifiers

PMID8421672
PMCPMC45677
OpenAlexW2036658784

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.