Evidence map›Paper›PMID 12738878›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2003

Fatty acid synthesis is essential in embryonic development: fatty acid synthase null mutants and most of the heterozygotes die in utero.

Subrahmanyam S Chirala, Hua Chang, Martin Matzuk, Lutfi Abu-Elheiga, Jianqiang Mao, Kathleen Mahon, Milton Finegold, Salih J Wakil

Open access · greenAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2003. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 120 papers.

0numbers the graph read from it
0cells of the map it votes in
120citing papers in PubMed
4.3field-weighted citation impact, top 5% 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

120 citing papers in PubMed, 237 citations in OpenAlex.

  1. Review
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  17. In-depth analysis ofLiver research (Beijing, China) · 2023
    Review
  18. Role of EGFR and FASN in breast cancer progression.Journal of cell communication and signaling · 2023
    Review
  19. Article
  20. Article

60 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

8 authors at 1 institution in 1 country.

Subrahmanyam S ChiralaVerna and Marrs McLean Department of Biochemistry and Molecular Biology, Baylor College of Medicine, Houston, TX 77030, USA.
Hua Chang
Martin Matzuk
Lutfi Abu-Elheiga
Jianqiang Mao
Kathleen Mahon
Milton Finegold
Salih J Wakil
Baylor College of Medicine · US

Funding

Role of the Acetyl-CoA Carboxylases in Energy MetabolismR01GM063115 · NIGMS · BAYLOR COLLEGE OF MEDICINE · PI WAKIL, SALIH JAWAD · 2002 to 2011
$3.2M
NIGMS NIH HHS GM-63115NIGMS NIH HHS R01 GM063115
6 · The paper itself

Abstract

In animals, including humans, the source of long-chain saturated fatty acids is de novo synthesis, which is mediated by fatty acid synthase (FAS), ingested food, or both. To understand the importance of de novo fatty acid synthesis, we generated FAS knockout mice. The heterozygous FAS mutants (Fasn+/-) are ostensibly normal. In Fasn+/- mice the levels of FAS mRNA and the FAS activity are approximately 50% and 35% lower, respectively, than those of WT mice; hence, FAS levels are affected by gene dosage. When the Fasn+/- mutant mice were interbred, Fasn-/- mice were not produced; thus, FAS is essential during embryonic development. Furthermore, the number of Fasn+/- progeny obtained was 70% less than predicted by Mendelian inheritance, indicating partial haploid insufficiency. Even when one of the parents was WT, the estimated loss of heterozygous progeny was 60%. This loss of Fasn+/- pups appeared to be strain-specific and became more pronounced as the heterozygous females produced more litters. Most of the Fasn-/- mutant embryos died before implantation and the Fasn+/- embryos died at various stages of their development. Feeding the breeders a diet rich in saturated fatty acids did not prevent the loss of homoor heterozygotes. These observations are very important in considering teratogenic consequences of drugs aimed at inhibiting FAS activity, to reduce either obesity or the growth of cancerous tissues.

Indexed as

HeterozygoteAnimalsBase SequenceDNA PrimersEmbryo, MammalianEmbryonic and Fetal DevelopmentFatty AcidsFatty Acid SynthasesFemaleGene Expression Regulation, EnzymologicMaleMiceMice, KnockoutDNA PrimersFatty AcidsFatty Acid Synthases

Identifiers

PMID12738878
PMCPMC164451
OpenAlexW2073387842

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.