Evidence map›Paper›PMID 20061394›Full record

ArticleThe Journal of biological chemistry2010

Alternative exon usage in the single CPT1 gene of Drosophila generates functional diversity in the kinetic properties of the enzyme: differential expression of alternatively spliced variants in Drosophila tissues.

Nigel T Price, Vicky N Jackson, Jürgen Müller, Kevin Moffat, Karen L Matthews, Tim Orton, Victor A Zammit

Open access · hybridAbstract read
In one paragraph

Article in The Journal of biological chemistry, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.1field-weighted citation impact, top 24% 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

6 citing papers in PubMed, 20 citations in OpenAlex.

  1. Transcriptional Control of Lipid Metabolism.Advances in experimental medicine and biology · 2026
    Review
  2. The regulation of carnitine palmitoyltransferase 1 (Biochemistry and biophysics reports · 2024
    Article
  3. Article
  4. Article
  5. The control of lipid metabolism by mRNA splicing in Drosophila.Biochemical and biophysical research communications · 2014
    Article
  6. 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 1 institution in 1 country.

Nigel T PriceWarwick Medical School, University of Warwick, Gibbett Hill Road, Coventry CV4 7AL, United Kingdom.
Vicky N Jackson
Jürgen Müller
Kevin Moffat
Karen L Matthews
Tim Orton
Victor A Zammit
University of Warwick · GB

Funding

British Heart Foundation
6 · The paper itself

Abstract

The Drosophila melanogaster genome contains only one CPT1 gene (Jackson, V. N., Cameron, J. M., Zammit, V. A., and Price, N. T. (1999) Biochem. J. 341, 483-489). We have now extended our original observation to all insect genomes that have been sequenced, suggesting that a single CPT1 gene is a universal feature of insect genomes. We hypothesized that insects may be able to generate kinetically distinct variants by alternative splicing of their single CPT1 gene. Analysis of the insect genomes revealed that (a) the single CPT1 gene in each and every insect genome contains two alternative exons and (ii) in all cases, the putative alternative splicing site occurs within a small region corresponding to 21 amino acid residues that are known to be essential for the binding of substrates and of malonyl-CoA in mammalian CPT1A. We performed PCR analyses of mRNA from different Drosophila tissues; both of the anticipated splice variants of CPT1 mRNA were found to be expressed in all of the tissues tested (both in larvae and adults), with the expression level for one of the splice variants being significantly different between flight muscle and the fat body of adult Drosophila. Heterologous expression of the full-length cDNAs corresponding to the two putative variants of Drosophila CPT1 in the yeast Pichia pastoris revealed two important differences between the properties of the two variants: (i) their affinity (K(0.5)) for one of the substrates, palmitoyl-CoA, differed by 5-fold, and (ii) the sensitivity to inhibition by malonyl-CoA at fixed, higher palmitoyl-CoA concentrations was 2-fold different and associated with different kinetics of inhibition. These data indicate that alternative splicing that specifically affects a structurally crucial region of the protein is an important mechanism through which functional diversity of CPT1 kinetics is generated from the single gene that occurs in insects.

Indexed as

AedesAlternative SplicingAmino Acid SequenceAnimalsAnophelesBase SequenceCarnitine O-PalmitoyltransferaseDNA, ComplementaryDrosophila melanogasterDrosophila ProteinsEnzyme InhibitorsExonsGene Expression Regulation, EnzymologicGenetic VariationKineticsMalonyl Coenzyme ACarnitine O-PalmitoyltransferaseDNA, ComplementaryDrosophila ProteinsEnzyme InhibitorsMalonyl Coenzyme ARNA, Messenger

Identifiers

PMID20061394
PMCPMC2832936
OpenAlexW1982722262

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.