Evidence map›Paper›PMID 39031128›Full record

ArticleJournal of experimental botany2024

Cuticle development and the underlying transcriptome-metabolome associations during early seedling establishment.

Keting Chen, Rupam Kumar Bhunia, Matthew M Wendt, Grace Campidilli, Colton McNinch, Ahmed Hassan, Ling Li, Basil J Nikolau, Marna D Yandeau-Nelson

Abstract read
In one paragraph

Article in Journal of experimental botany, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. 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

9 authors.

Keting ChenDepartment of Genetics, Development & Cell Biology, Iowa State University, Ames, IA, USA.ORCID 0000-0002-5242-7239
Rupam Kumar BhuniaRoy J. Carver Department of Biochemistry, Biophysics & Molecular Biology, Iowa State University, Ames, IA, USA.ORCID 0000-0001-7303-5050
Matthew M WendtDepartment of Genetics, Development & Cell Biology, Iowa State University, Ames, IA, USA.
Grace CampidilliDepartment of Genetics, Development & Cell Biology, Iowa State University, Ames, IA, USA.
Colton McNinchMolecular, Cellular, and Developmental Biology Graduate Program, Iowa State University, Ames, IA, USA.ORCID 0000-0003-2545-1177
Ahmed HassanDepartment of Genetics, Development & Cell Biology, Iowa State University, Ames, IA, USA.
Ling LiDepartment of Biological Sciences, Mississippi State University, Mississippi State, MS, USA.ORCID 0000-0003-2371-6215
Basil J NikolauRoy J. Carver Department of Biochemistry, Biophysics & Molecular Biology, Iowa State University, Ames, IA, USA.ORCID 0000-0002-4672-7139
Marna D Yandeau-NelsonDepartment of Genetics, Development & Cell Biology, Iowa State University, Ames, IA, USA.ORCID 0000-0002-2742-7384

Funding

The NSF IOS-1354799United States Department of Energy DE-SC18519
6 · The paper itself

Abstract

The plant cuticle is a complex extracellular lipid barrier that has multiple protective functions. This study investigated cuticle deposition by integrating metabolomics and transcriptomics data gathered from six different maize seedling organs of four genotypes, the inbred lines B73 and Mo17, and their reciprocal hybrids. These datasets captured the developmental transition of the seedling from heterotrophic skotomorphogenic growth to autotrophic photomorphogenic growth, a transition that is highly vulnerable to environmental stresses. Statistical interrogation of these data revealed that the predominant determinant of cuticle composition is seedling organ type, whereas the seedling genotype has a smaller effect on this phenotype. Gene-to-metabolite associations assessed by integrated statistical analyses identified three gene networks associated with the deposition of different elements of the cuticle: cuticular waxes; monomers of lipidized cell wall biopolymers, including cutin and suberin; and both of these elements. These gene networks reveal three metabolic programs that appear to support cuticle deposition, including processes of chloroplast biogenesis, lipid metabolism, and molecular regulation (e.g. transcription factors, post-translational regulators, and phytohormones). This study demonstrates the wider physiological metabolic context that can determine cuticle deposition and lays the groundwork for new targets for modulating the properties of this protective barrier.

Indexed as

MetabolomeSeedlingsTranscriptomeZea maysGene Expression Regulation, PlantWaxesWaxesCuticlecuticular waxescutinearly seedling establishmentgene networksjoint transcriptome–metabolome analysismaize

Identifiers

PMID39031128
PMCPMC11522977

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.