Evidence map›Paper›PMID 29940865›Full record

ArticleBMC plant biology2018

Auxin analysis using laser microdissected plant tissues sections.

Luz G Muñoz-Sanhueza, YeonKyeong Lee, Molly Tillmann, Jerry D Cohen, Anne Kathrine Hvoslef-Eide

Open access · goldAbstract read
In one paragraph

Article in BMC plant biology, 2018. 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
1.4field-weighted citation impact, top 14% 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

4 citing papers in PubMed, 6 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

5 authors at 2 institutions in 2 countries.

Luz G Muñoz-SanhuezaDepartment of Plant Sciences (IPV), Faculty of Biosciences, Norwegian University of Life Sciences, Norway Campus Ås, Universitetstunet 3, 1430, Ås, Norway.
YeonKyeong LeeDepartment of Plant Sciences (IPV), Faculty of Biosciences, Norwegian University of Life Sciences, Norway Campus Ås, Universitetstunet 3, 1430, Ås, Norway.
Molly TillmannDepartment of Horticultural Sciences, Microbial and Plant Genomics Institute, University of Minnesota, 305 Alderman Hall, 1970 Folwell Avenue, Saint Paul, MN, 55108, USA.
Jerry D CohenDepartment of Horticultural Sciences, Microbial and Plant Genomics Institute, University of Minnesota, 305 Alderman Hall, 1970 Folwell Avenue, Saint Paul, MN, 55108, USA.
Anne Kathrine Hvoslef-EideDepartment of Plant Sciences (IPV), Faculty of Biosciences, Norwegian University of Life Sciences, Norway Campus Ås, Universitetstunet 3, 1430, Ås, Norway. trine.hvoslef-eide@nmbu.no.ORCID http://orcid.org/0000-0002-4826-8423
Norwegian University of Life Sciences · NOUniversity of Minnesota · US

Funding

National Science Foundation (IOS-1238812)
6 · The paper itself

Abstract

backgroundQuantitative measurement of actual auxin levels in plant tissue is complimentary to molecular methods measuring the expression of auxin related genes. Current analytical methods to quantify auxin have pushed the limit of detection to where auxin can be routinely quantified at the pictogram (pg) level, reducing the amount of tissue needed to perform these kinds of studies to amounts never imagined a few years ago. In parallel, the development of technologies like laser microdissection microscopy (LMD) has allowed specific cells to be harvested from discrete tissues without including adjacent cells. This method has gained popularity in recent years, especially for enabling a higher degree of spatial resolution in transcriptome profiling. As with other quantitative measurements, including hormone quantifications, sampling using traditional LMD is still challenging because sample preparation clearly compromises the preservation of analytes. Thus, we have developed and validated a sample preparation protocol combining cryosectioning, freeze-drying, and capturing with a laser microdissection microscope to provide high-quality and well-preserved plant materials suitable for ultrasensitive, spatially-resolved auxin quantification.

resultsWe developed a new method to provide discrete plant tissues for indole-3-acetic acid (IAA) quantification while preserving the plant tissue in the best possible condition to prevent auxin degradation. The method combines the use of cryosectioning, freeze-drying and LMD. The protocol may also be used for other applications that require small molecule analysis with high tissue-specificity where degradation of biological compounds may be an issue. It was possible to collect the equivalent to 15 mg of very specific tissue in approximately 4 h using LMD.

conclusionsWe have shown, by proof of concept, that freeze dried cryosections of plant tissue were suitable for LMD harvest and quantification of the phytohormone auxin using GC-MS/MS. We expect that the ability to resolve auxin levels with both spatial- and temporal resolution with high accuracy will enable experiments on complex processes, which will increase our knowledge of the many roles of auxins (and, in time, other phytohormones) in plant development.

Indexed as

CryoultramicrotomyEuphorbiaFlowersFreeze DryingGas Chromatography-Mass SpectrometryIndoleacetic AcidsLaser Capture MicrodissectionLimit of DetectionPlant Growth RegulatorsPlant LeavesPlantsIndoleacetic AcidsPlant Growth RegulatorsAuxin quantificationCryosectioningFreeze dryingGC-MS/MS quantificationIsotope dilution analysisLaser microdissection microscopeLyophilisationMinute samplesPlant sample preparation

Identifiers

PMID29940865
PMCPMC6019200
OpenAlexW2810589082

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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.