Evidence map›Paper›PMID 25660346›Full record

ArticleAnnals of botany2015

Inherited phenotype instability of inflorescence and floral organ development in homeotic barley double mutants and its specific modification by auxin inhibitors and 2,4-D.

Raimondas Šiukšta, Virginija Vaitkūnienė, Greta Kaselytė, Vaiva Okockytė, Justina Žukauskaitė, Donatas Žvingila, Vytautas Rančelis

Open access · bronzeAbstract read
In one paragraph

Article in Annals of botany, 2015. 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
1.6field-weighted citation impact, top 13% 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, 9 citations in OpenAlex.

  1. Article
  2. Expression of Specific Alleles of Zinc-Finger Transcription Factors,International journal of molecular sciences · 2021
    Article
  3. Article
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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

7 authors at 1 institution in 1 country.

Raimondas ŠiukštaDepartment of Botany and Genetics, Faculty of Natural Sciences, Vilnius University, M. K. Čiurlionis Str. 21/27, LT-03101 Vilnius, Lithuania and Botanical Garden of Vilnius University, Kairėnai Str. 43, LT-10239 Vilnius, Lithuania Department of Botany and Genetics, Faculty of Natural Sciences, Vilnius University, M. K. Čiurlionis Str. 21/27, LT-03101 Vilnius, Lithuania and Botanical Garden of Vilnius University, Kairėnai Str. 43, LT-10239 Vilnius, Lithuania Raimondas.Siuksta@gf.vu.lt.
Virginija VaitkūnienėDepartment of Botany and Genetics, Faculty of Natural Sciences, Vilnius University, M. K. Čiurlionis Str. 21/27, LT-03101 Vilnius, Lithuania and Botanical Garden of Vilnius University, Kairėnai Str. 43, LT-10239 Vilnius, Lithuania Department of Botany and Genetics, Faculty of Natural Sciences, Vilnius University, M. K. Čiurlionis Str. 21/27, LT-03101 Vilnius, Lithuania and Botanical Garden of Vilnius University, Kairėnai Str. 43, LT-10239 Vilnius, Lithuania.
Greta KaselytėDepartment of Botany and Genetics, Faculty of Natural Sciences, Vilnius University, M. K. Čiurlionis Str. 21/27, LT-03101 Vilnius, Lithuania and Botanical Garden of Vilnius University, Kairėnai Str. 43, LT-10239 Vilnius, Lithuania.
Vaiva OkockytėDepartment of Botany and Genetics, Faculty of Natural Sciences, Vilnius University, M. K. Čiurlionis Str. 21/27, LT-03101 Vilnius, Lithuania and Botanical Garden of Vilnius University, Kairėnai Str. 43, LT-10239 Vilnius, Lithuania.
Justina ŽukauskaitėDepartment of Botany and Genetics, Faculty of Natural Sciences, Vilnius University, M. K. Čiurlionis Str. 21/27, LT-03101 Vilnius, Lithuania and Botanical Garden of Vilnius University, Kairėnai Str. 43, LT-10239 Vilnius, Lithuania.
Donatas ŽvingilaDepartment of Botany and Genetics, Faculty of Natural Sciences, Vilnius University, M. K. Čiurlionis Str. 21/27, LT-03101 Vilnius, Lithuania and Botanical Garden of Vilnius University, Kairėnai Str. 43, LT-10239 Vilnius, Lithuania.
Vytautas RančelisDepartment of Botany and Genetics, Faculty of Natural Sciences, Vilnius University, M. K. Čiurlionis Str. 21/27, LT-03101 Vilnius, Lithuania and Botanical Garden of Vilnius University, Kairėnai Str. 43, LT-10239 Vilnius, Lithuania.
Vilnius University · LT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimsBarley (Hordeum vulgare) double mutants Hv-Hd/tw2, formed by hybridization, are characterized by inherited phenotypic instability and by several new features, such as bract/leaf-like structures, long naked gaps in the spike, and a wide spectrum of variations in the basic and ectopic flowers, which are absent in single mutants. Several of these features resemble those of mutations in auxin distribution, and thus the aim of this study was to determine whether auxin imbalances are related to phenotypic variations and instability. The effects of auxin inhibitors and 2,4-D (2,4-dichlorophenoxyacetic acid) on variation in basic and ectopic flowers were therefore examined, together with the effects of 2,4-D on spike structure.

methodsThe character of phenotypic instability and the effects of auxin inhibitors and 2,4-D were compared in callus cultures and intact plants of single homeotic Hv-tw2 and Hv-Hooded/Kap (in the BKn3 gene) mutants and alternative double mutant lines: offspring from individual plants in distal hybrid generations (F9-F10) that all had the same BKn3 allele as determined by DNA sequencing. For intact plants, two auxin inhibitors, 9-hydroxyfluorene-9-carboxylic acid (HFCA) and p-chlorophenoxyisobutyric acid (PCIB), were used. KEY

resultsCallus growth and flower/spike structures of the Hv-tw2 mutant differed in their responses to HFCA and PCIB. An increase in normal basic flowers after exposure to auxin inhibitors and a decrease in their frequencies caused by 2,4-D were observed, and there were also modifications in the spectra of ectopic flowers, especially those with sexual organs, but the effects depended on the genotype. Exposure to 2,4-D decreased the frequency of short gaps and lodicule transformations in Hv-tw2 and of long naked gaps in double mutants.

conclusionsThe effects of auxin inhibitors and 2,4-D suggest that ectopic auxin maxima or deficiencies arise in various regions of the inflorescence/flower primordia. Based on the phenotypic instability observed, definite trends in the development of ectopic flower structures may be detected, from insignificant outgrowths on awns to flowers with sterile organs. Phenotypically unstable barley double mutants provide a highly promising genetic system for the investigation of gene expression modules and trend orders.

Indexed as

HordeumMutation2,4-Dichlorophenoxyacetic AcidCarboxylic AcidsClofibric AcidFlowersIndoleacetic AcidsPhenotypePlant Growth RegulatorsPlant Proteins2,4-Dichlorophenoxyacetic AcidCarboxylic AcidsClofibric AcidIndoleacetic AcidsPlant Growth RegulatorsPlant Proteins24-DAuxin inhibitorsbarleydouble mutantsfloral organ growthflower developmentflower structurehomeotic mutantsHordeum vulgarephenotypic instabilityspecific normalization

Identifiers

PMID25660346
PMCPMC4343296
OpenAlexW2329007388

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