Evidence map›Paper›PMID 26798115›Full record

ArticleGenome biology and evolution2016

Identification of Sequences Encoding Symbiodinium minutum Mitochondrial Proteins.

Erin R Butterfield, Christopher J Howe, R Ellen R Nisbet

Open access · goldAbstract read
In one paragraph

Article in Genome biology and evolution, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.5field-weighted citation impact, top 29% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. 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

3 authors at 1 institution in 2 countries.

Erin R ButterfieldSchool of Pharmacy and Medical Sciences, Sansom Institute for Health Research, University of South Australia, North Terrace, Adelaide, SA, Australia Department of Biochemistry, University of Cambridge, Cambridge, Cambridgeshire, United Kingdom.
Christopher J HoweDepartment of Biochemistry, University of Cambridge, Cambridge, Cambridgeshire, United Kingdom.
R Ellen R NisbetSchool of Pharmacy and Medical Sciences, Sansom Institute for Health Research, University of South Australia, North Terrace, Adelaide, SA, Australia Department of Biochemistry, University of Cambridge, Cambridge, Cambridgeshire, United Kingdom rern2@cam.ac.uk.
University of Cambridge · GB

Funding

Wellcome TrustWellcome Trust WT094249
6 · The paper itself

Abstract

The dinoflagellates are an extremely diverse group of algae closely related to the Apicomplexa and the ciliates. Much work has previously been undertaken to determine the presence of various biochemical pathways within dinoflagellate mitochondria. However, these studies were unable to identify several key transcripts including those encoding proteins involved in the pyruvate dehydrogenase complex, iron-sulfur cluster biosynthesis, and protein import. Here, we analyze the draft nuclear genome of the dinoflagellate Symbiodinium minutum, as well as RNAseq data to identify nuclear genes encoding mitochondrial proteins. The results confirm the presence of a complete tricarboxylic acid cycle in the dinoflagellates. Results also demonstrate the difficulties in using the genome sequence for the identification of genes due to the large number of introns, but show that it is highly useful for the determination of gene duplication events.

Indexed as

Citric Acid CycleDinoflagellidaIntronsMitochondrial ProteinsProtozoan ProteinsRNA, MessengerMitochondrial ProteinsProtozoan ProteinsRNA, Messengeralveolatechloroplastdinoflagellatemetabolismmitochondria

Identifiers

PMID26798115
PMCPMC4779609
OpenAlexW2278463277

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.