Evidence map›Paper›PMID 33258946›Full record

ArticleJournal of experimental botany2021

Protein phosphatase NtPP2C2b and MAP kinase NtMPK4 act in concert to modulate nicotine biosynthesis.

Xiaoyu Liu, Sanjay Kumar Singh, Barunava Patra, Yongliang Liu, Bingwu Wang, Jinsheng Wang, Sitakanta Pattanaik, Ling Yuan

Open access · hybridAbstract read
In one paragraph

Article in Journal of experimental botany, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
3.0field-weighted citation impact, top 9% 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

12 citing papers in PubMed, 22 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. Review
  10. Article
  11. Frontiers in plant science · 2022
    Article
  12. Review
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 3 institutions in 2 countries.

Xiaoyu LiuCollege of Agriculture, Shanxi Agricultural University, Taigu, Shanxi, China.
Sanjay Kumar SinghDepartment of Plant and Soil Sciences, and the Kentucky Tobacco Research and Development Center, University of Kentucky, University Drive, Lexington, KY USA.
Barunava PatraDepartment of Plant and Soil Sciences, and the Kentucky Tobacco Research and Development Center, University of Kentucky, University Drive, Lexington, KY USA.
Yongliang LiuDepartment of Plant and Soil Sciences, and the Kentucky Tobacco Research and Development Center, University of Kentucky, University Drive, Lexington, KY USA.
Bingwu WangTobacco Breeding Center, Yunnan Academy of Tobacco Agricultural Sciences, Kunming, Yunnan, China.
Jinsheng WangCollege of Agriculture, Shanxi Agricultural University, Taigu, Shanxi, China.
Sitakanta PattanaikDepartment of Plant and Soil Sciences, and the Kentucky Tobacco Research and Development Center, University of Kentucky, University Drive, Lexington, KY USA.
Ling YuanDepartment of Plant and Soil Sciences, and the Kentucky Tobacco Research and Development Center, University of Kentucky, University Drive, Lexington, KY USA.
University of Kentucky · USShanxi Agricultural University · CNYunnan Academy of Agricultural Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Protein phosphatases (PPs) and protein kinases (PKs) regulate numerous developmental, defense, and phytohormone signaling processes in plants. However, the underlying regulatory mechanism governing biosynthesis of specialized metabolites, such as alkaloids, by the combined effects of PPs and PKs, is insufficiently understood. Here, we report the characterization of a group B protein phosphatase type 2C, NtPP2C2b, that likely acts upstream of the NICOTINE2 locus APETALA 2/Ethylene Response Factors (AP2/ERFs), to regulate nicotine biosynthesis in tobacco. Similar to the nicotine pathway genes, NtPP2C2b is highly expressed in roots and induced by jasmonic acid (JA). Overexpression of NtPP2C2b in transgenic hairy roots or stable transgenic tobacco plants repressed nicotine pathway gene expression and reduced nicotine accumulation. Additionally, transient overexpression of NtPP2C2b, together with the NtERF221, repressed transactivation of the quinolinate phosphoribosyltransferase promoter in tobacco cells. We further demonstrate that the JA-responsive tobacco mitogen-activated protein kinase (MAPK) 4 interacts with NtPP2C2b in yeast and plant cells. Conditional overexpression of NtMPK4 in tobacco hairy roots up-regulated nicotine pathway gene expression and increased nicotine accumulation. Our findings suggest that a previously uncharacterized PP-PK module acts to modulate alkaloid biosynthesis, highlighting the importance of post-translational control in the biosynthesis of specialized plant metabolites.

Indexed as

Mitogen-Activated Protein KinasesNicotianaPhosphoprotein PhosphatasesPlant ProteinsCyclopentanesGene Expression Regulation, PlantNicotineOxylipinsPlant RootsPlants, Genetically ModifiedTranscription FactorsCyclopentanesMitogen-Activated Protein KinasesNicotineOxylipinsPhosphoprotein PhosphatasesPlant ProteinsTranscription FactorsAlkaloid biosynthesisgene regulationhairy rootsMAP kinasenicotineprotein phosphatase 2Csecondary metabolismtobacco

Identifiers

PMID33258946
PMCPMC7921305
OpenAlexW3107650727

What Socratic 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 Socratic graph.