Evidence map›Paper›PMID 28345615›Full record

ArticleScientific reports2017

Transcriptome analysis of molecular mechanisms responsible for light-stress response in Mythimna separata (Walker).

Yun Duan, ZhongJun Gong, RenHai Wu, Jin Miao, YueLi Jiang, Tong Li, XiaoBo Wu, YuQing Wu

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
3.3field-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

9 citing papers in PubMed, 30 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. AnInsects · 2023
    Article
  5. Article
  6. Evolution of Phototransduction Genes in Lepidoptera.Genome biology and evolution · 2019
    Article
  7. Article
  8. Article
  9. 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

8 authors at 2 institutions in 1 country.

Yun DuanInstitute of Plant Protection, Henan Academy of Agricultural Sciences, Key Laboratory of Crop Pest Control of Henan Province, Key Laboratory of Integrated Pest Management on Crops in Southern Region of North China, Zhengzhou 450002, China.
ZhongJun GongInstitute of Plant Protection, Henan Academy of Agricultural Sciences, Key Laboratory of Crop Pest Control of Henan Province, Key Laboratory of Integrated Pest Management on Crops in Southern Region of North China, Zhengzhou 450002, China.
RenHai WuInstitute of Plant Protection, Henan Academy of Agricultural Sciences, Key Laboratory of Crop Pest Control of Henan Province, Key Laboratory of Integrated Pest Management on Crops in Southern Region of North China, Zhengzhou 450002, China.
Jin MiaoInstitute of Plant Protection, Henan Academy of Agricultural Sciences, Key Laboratory of Crop Pest Control of Henan Province, Key Laboratory of Integrated Pest Management on Crops in Southern Region of North China, Zhengzhou 450002, China.
YueLi JiangInstitute of Plant Protection, Henan Academy of Agricultural Sciences, Key Laboratory of Crop Pest Control of Henan Province, Key Laboratory of Integrated Pest Management on Crops in Southern Region of North China, Zhengzhou 450002, China.
Tong LiInstitute of Plant Protection, Henan Academy of Agricultural Sciences, Key Laboratory of Crop Pest Control of Henan Province, Key Laboratory of Integrated Pest Management on Crops in Southern Region of North China, Zhengzhou 450002, China.
XiaoBo WuInstitute of Plant Protection, Henan Academy of Agricultural Sciences, Key Laboratory of Crop Pest Control of Henan Province, Key Laboratory of Integrated Pest Management on Crops in Southern Region of North China, Zhengzhou 450002, China.
YuQing WuInstitute of Plant Protection, Henan Academy of Agricultural Sciences, Key Laboratory of Crop Pest Control of Henan Province, Key Laboratory of Integrated Pest Management on Crops in Southern Region of North China, Zhengzhou 450002, China.
Institute of Plant Protection · CNHenan Academy of Agricultural Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Light is an important environmental signal for most insects. The Oriental Armyworm, Mythimna separata, is a serious pest of cereal crops worldwide, and is highly sensitive to light signals during its developmental and reproductive stages. However, molecular biological studies of its response to light stress are scarce, and related genomic information is not available. In this study, we sequenced and de novo assembled the transcriptomes of M. separata exposed to four different light conditions: dark, white light (WL), UV light (UVL) and yellow light (YL). A total of 46,327 unigenes with an average size of 571 base pairs (bp) were obtained, among which 24,344 (52.55%) matched to public databases. The numbers of genes differentially expressed between dark vs WL, dark vs UVL, dark vs YL, and UVL vs YL were 12,012, 12,950, 14,855, and 13,504, respectively. These results suggest that light exposure altered gene expression patterns in M. separata. Putative genes involved in phototransduction-fly, phototransduction, circadian rhythm-fly, olfactory transduction, and taste transduction were identified. This study thus identified a series of candidate genes and pathways potentially related to light stress in M. separata.

Indexed as

Stress, PhysiologicalAnimalsFemaleGene Expression ProfilingGene Expression RegulationHigh-Throughput Nucleotide SequencingInsect ProteinsLightMaleMothsOpen Reading FramesSequence Analysis, RNAInsect Proteins

Identifiers

PMID28345615
PMCPMC5367045
OpenAlexW2600750165

What OpenQuestion 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 OpenQuestion graph.