Evidence map›Paper›PMID 28192486›Full record

ArticlePloS one2017

Ocean acidification modulates expression of genes and physiological performance of a marine diatom.

Yahe Li, Shufang Zhuang, Yaping Wu, Honglin Ren, Fangyi Chen, Xin Lin, Kejian Wang, John Beardall, Kunshan Gao

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
3.1field-weighted citation impact, top 10% 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

7 citing papers in PubMed, 19 citations in OpenAlex.

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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

9 authors at 3 institutions in 2 countries.

Yahe LiState Key Laboratory of Marine Environmental Science (Xiamen University), College of Ocean and Earth Sciences, Xiamen University, Xiamen, China.
Shufang ZhuangState Key Laboratory of Marine Environmental Science (Xiamen University), College of Ocean and Earth Sciences, Xiamen University, Xiamen, China.
Yaping WuState Key Laboratory of Marine Environmental Science (Xiamen University), College of Ocean and Earth Sciences, Xiamen University, Xiamen, China.
Honglin RenKey Laboratory of Zoonosis Research, Ministry of Education, Institute of Zoonosis, Jilin University, Changchun, China.
Fangyi ChenState Key Laboratory of Marine Environmental Science (Xiamen University), College of Ocean and Earth Sciences, Xiamen University, Xiamen, China.
Xin LinState Key Laboratory of Marine Environmental Science (Xiamen University), College of Ocean and Earth Sciences, Xiamen University, Xiamen, China.
Kejian WangState Key Laboratory of Marine Environmental Science (Xiamen University), College of Ocean and Earth Sciences, Xiamen University, Xiamen, China.
John BeardallSchool of Biological Sciences, Monash University, Clayton, Victoria, Australia.
Kunshan GaoState Key Laboratory of Marine Environmental Science (Xiamen University), College of Ocean and Earth Sciences, Xiamen University, Xiamen, China.
Xiamen University · CNJilin University · CNMonash University · AU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ocean Acidification (OA) is known to affect various aspects of physiological performances of diatoms, but little is known about the underlining molecular mechanisms involved. Here, we show that in the model diatom Phaeodactylum tricornutum, the expression of key genes associated with photosynthetic light harvesting as well as those encoding Rubisco, carbonic anhydrase, NADH dehydrogenase and nitrite reductase, are modulated by OA (1000 μatm, pHnbs 7.83). Growth and photosynthetic carbon fixation were enhanced by elevated CO2. OA treatment decreased the expression of β-carbonic anhydrase (β-ca), which functions in balancing intracellular carbonate chemistry and the CO2 concentrating mechanism (CCM). The expression of the genes encoding fucoxanthin chlorophyll a/c protein (lhcf type (fcp)), mitochondrial ATP synthase (mtATP), ribulose-1, 5-bisphosphate carboxylase/oxygenase large subunit gene (rbcl) and NADH dehydrogenase subunit 2 (ndh2), were down-regulated during the first four days (< 8 generations) after the cells were transferred from LC (cells grown under ambient air condition; 390 μatm; pHnbs 8.19) to OA conditions, with no significant difference between LC and HC treatments with the time elapsed. The expression of nitrite reductase (nir) was up-regulated by the OA treatment. Additionally, the genes for these proteins (NiR, FCP, mtATP synthase, β-CA) showed diel expression patterns. It appeared that the enhanced photosynthetic and growth rates under OA could be attributed to stimulated nitrogen assimilation, increased CO2 availability or saved energy from down-regulation of the CCM and consequently lowered cost of protein synthesis versus that of non-nitrogenous cell components.

Indexed as

Gene Expression Regulation, DevelopmentalCarbonCarbon DioxideCarbonic AnhydrasesChlorophyllDiatomsDown-RegulationHydrogen-Ion ConcentrationNADH DehydrogenaseNitrite ReductasesNitrogenOceans and SeasPhotosynthesisReverse Transcriptase Polymerase Chain ReactionRibulose-Bisphosphate CarboxylaseSeawaterCarbonCarbon DioxideCarbonic AnhydrasesChlorophyllNADH DehydrogenaseNitrite ReductasesNitrogenRibulose-Bisphosphate Carboxylase

Identifiers

PMID28192486
PMCPMC5305191
OpenAlexW2588269297

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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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.