Evidence map›Paper›PMID 29946328›Full record

ArticleFrontiers in plant science2018

Prioritization of Candidate Genes in QTL Regions for Physiological and Biochemical Traits Underlying Drought Response in Barley (

Kornelia Gudys, Justyna Guzy-Wrobelska, Agnieszka Janiak, Michał A Dziurka, Agnieszka Ostrowska, Katarzyna Hura, Barbara Jurczyk, Katarzyna Żmuda, Daria Grzybkowska, Joanna Śróbka and 10 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in plant science, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
5.4field-weighted citation impact, top 5% 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

21 citing papers in PubMed, 45 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

20 authors at 4 institutions in 1 country.

Kornelia GudysDepartment of Genetics, Faculty of Biology and Environmental Protection, University of Silesia, Katowice, Poland.
Justyna Guzy-WrobelskaDepartment of Genetics, Faculty of Biology and Environmental Protection, University of Silesia, Katowice, Poland.
Agnieszka JaniakDepartment of Genetics, Faculty of Biology and Environmental Protection, University of Silesia, Katowice, Poland.
Michał A DziurkaDepartment of Developmental Biology, Institute of Plant Physiology, Polish Academy of Sciences, Krakow, Poland.
Agnieszka OstrowskaDepartment of Developmental Biology, Institute of Plant Physiology, Polish Academy of Sciences, Krakow, Poland.
Katarzyna HuraDepartment of Plant Physiology, Faculty of Agriculture and Economics, University of Agriculture, Krakow, Poland.
Barbara JurczykDepartment of Plant Physiology, Faculty of Agriculture and Economics, University of Agriculture, Krakow, Poland.
Katarzyna ŻmudaDepartment of Plant Physiology, Faculty of Agriculture and Economics, University of Agriculture, Krakow, Poland.
Daria GrzybkowskaDepartment of Genetics, Faculty of Biology and Environmental Protection, University of Silesia, Katowice, Poland.
Joanna ŚróbkaDepartment of Genetics, Faculty of Biology and Environmental Protection, University of Silesia, Katowice, Poland.
Wojciech UrbanDepartment of Genetics, Faculty of Biology and Environmental Protection, University of Silesia, Katowice, Poland.
Jolanta Biesaga-KoscielniakDepartment of Developmental Biology, Institute of Plant Physiology, Polish Academy of Sciences, Krakow, Poland.
Maria FilekDepartment of Developmental Biology, Institute of Plant Physiology, Polish Academy of Sciences, Krakow, Poland.
Janusz KoscielniakDepartment of Plant Physiology, Faculty of Agriculture and Economics, University of Agriculture, Krakow, Poland.
Krzysztof MikołajczakDepartment of Biotechnology, Institute of Plant Genetics, Polish Academy of Sciences, Poznan, Poland.
Piotr OgrodowiczDepartment of Biotechnology, Institute of Plant Genetics, Polish Academy of Sciences, Poznan, Poland.
Karolina KrystkowiakDepartment of Biotechnology, Institute of Plant Genetics, Polish Academy of Sciences, Poznan, Poland.
Anetta KuczyńskaDepartment of Biotechnology, Institute of Plant Genetics, Polish Academy of Sciences, Poznan, Poland.
Paweł KrajewskiDepartment of Biometry and Bioinformatics, Institute of Plant Genetics, Polish Academy of Sciences, Poznan, Poland.
Iwona SzarejkoDepartment of Genetics, Faculty of Biology and Environmental Protection, University of Silesia, Katowice, Poland.
Polish Academy of Sciences · PLUniversity of Silesia in Katowice · PLUniversity of Agriculture in Krakow · PLInstitute of Plant Genetics, Polish Academy of Sciences · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Drought is one of the most adverse abiotic factors limiting growth and productivity of crops. Among them is barley, ranked fourth cereal worldwide in terms of harvested acreage and production. Plants have evolved various mechanisms to cope with water deficit at different biological levels, but there is an enormous challenge to decipher genes responsible for particular complex phenotypic traits, in order to develop drought tolerant crops. This work presents a comprehensive approach for elucidation of molecular mechanisms of drought tolerance in barley at the seedling stage of development. The study includes mapping of QTLs for physiological and biochemical traits associated with drought tolerance on a high-density function map, projection of QTL confidence intervals on barley physical map, and the retrievement of positional candidate genes (CGs), followed by their prioritization based on Gene Ontology (GO) enrichment analysis. A total of 64 QTLs for 25 physiological and biochemical traits that describe plant water status, photosynthetic efficiency, osmoprotectant and hormone content, as well as antioxidant activity, were positioned on a consensus map, constructed using RIL populations developed from the crosses between European and Syrian genotypes. The map contained a total of 875 SNP, SSR and CGs, spanning 941.86 cM with resolution of 1.1 cM. For the first time, QTLs for ethylene, glucose, sucrose, maltose, raffinose, α-tocopherol, γ-tocotrienol content, and catalase activity, have been mapped in barley. Based on overlapping confidence intervals of QTLs, 11 hotspots were identified that enclosed more than 60% of mapped QTLs. Genetic and physical map integration allowed the identification of 1,101 positional CGs within the confidence intervals of drought response-specific QTLs. Prioritization resulted in the designation of 143 CGs, among them were genes encoding antioxidants, carboxylic acid biosynthesis enzymes, heat shock proteins, small auxin up-regulated RNAs, nitric oxide synthase, ATP sulfurylases, and proteins involved in regulation of flowering time. This global approach may be proposed for identification of new CGs that underlies QTLs responsible for complex traits.

Indexed as

barleyCG prioritizationdrought tolerancefunction mapGO enrichmentQTLQTL hotspot

Identifiers

PMID29946328
PMCPMC6005862
OpenAlexW2804144684

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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.