Evidence map›Paper›PMID 29912355›Full record

ArticleJournal of experimental botany2018

Physiological performance of transplastomic tobacco plants overexpressing aquaporin AQP1 in chloroplast membranes.

Alicia Fernández-San Millán, Iker Aranjuelo, Cyril Douthe, Miquel Nadal, María Ancín, Luis Larraya, Inmaculada Farran, Jaume Flexas, Jon Veramendi

Open access · hybridAbstract read
In one paragraph

Article in Journal of experimental botany, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
0.7field-weighted citation impact, top 30% 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

9 citing papers in PubMed, 14 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Expression of a COeLife · 2021
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  5. Review
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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.

Alicia Fernández-San MillánInstituto de Agrobiotecnología (Universidad Pública de Navarra-CSIC), Departamento de Producción Agraria, Campus Arrosadía, Pamplona, Spain.
Iker AranjueloInstituto de Agrobiotecnología (Universidad Pública de Navarra-CSIC), Departamento de Producción Agraria, Campus Arrosadía, Pamplona, Spain.
Cyril DoutheResearch Group on Plant Biology under Mediterranean Conditions, Departament de Biologia, Universitat de les Illes Balears, Carretera de Valldemossa, Palma de Mallorca, Illes Balears, Spain.
Miquel NadalResearch Group on Plant Biology under Mediterranean Conditions, Departament de Biologia, Universitat de les Illes Balears, Carretera de Valldemossa, Palma de Mallorca, Illes Balears, Spain.
María AncínInstituto de Agrobiotecnología (Universidad Pública de Navarra-CSIC), Departamento de Producción Agraria, Campus Arrosadía, Pamplona, Spain.
Luis LarrayaInstituto de Agrobiotecnología (Universidad Pública de Navarra-CSIC), Departamento de Producción Agraria, Campus Arrosadía, Pamplona, Spain.
Inmaculada FarranInstituto de Agrobiotecnología (Universidad Pública de Navarra-CSIC), Departamento de Producción Agraria, Campus Arrosadía, Pamplona, Spain.
Jaume FlexasResearch Group on Plant Biology under Mediterranean Conditions, Departament de Biologia, Universitat de les Illes Balears, Carretera de Valldemossa, Palma de Mallorca, Illes Balears, Spain.
Jon VeramendiInstituto de Agrobiotecnología (Universidad Pública de Navarra-CSIC), Departamento de Producción Agraria, Campus Arrosadía, Pamplona, Spain.
Universidad Publica de Navarra · ESUniversitat de les Illes Balears · ESÉcole nationale des ponts et chaussées · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The leaf mesophyll CO2 conductance and the concentration of CO2 within the chloroplast are major factors affecting photosynthetic performance. Previous studies have shown that the aquaporin NtAQP1 (which localizes to the plasma membrane and chloroplast inner envelope membrane) is involved in CO2 permeability in the chloroplast. Levels of NtAQP1 in plants genetically engineered to overexpress the protein correlated positively with leaf mesophyll CO2 conductance and photosynthetic rate. In these studies, the nuclear transformation method used led to changes in NtAQP1 levels in the plasma membrane and the chloroplast inner envelope membrane. In the present work, NtAQP1 levels were increased up to 16-fold in the chloroplast membranes alone by the overexpression of NtAQP1 from the plastid genome. Despite the high NtAQP1 levels achieved, transplastomic plants showed lower photosynthetic rates than wild-type plants. This result was associated with lower Rubisco maximum carboxylation rate and ribulose 1,5-bisphosphate regeneration. Transplastomic plants showed reduced mesophyll CO2 conductance but no changes in chloroplast CO2 concentration. The absence of differences in chloroplast CO2 concentration was associated with the lower CO2 fixation activity of the transplastomic plants. These findings suggest that non-functional pores of recombinant NtAQP1 may be produced in the chloroplast inner envelope membrane.

Indexed as

AquaporinsBiological TransportCarbon DioxideChloroplastsGene ExpressionNicotianaPlant ProteinsAquaporinsCarbon DioxidePlant Proteins

Identifiers

PMID29912355
PMCPMC6022695
OpenAlexW2800564869

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.