Evidence map›Paper›PMID 36307800›Full record

ArticleBMC biology2022

Transposable element expansion and low-level piRNA silencing in grasshoppers may cause genome gigantism.

Xuanzeng Liu, Muhammad Majid, Hao Yuan, Huihui Chang, Lina Zhao, Yimeng Nie, Lang He, Xiaojing Liu, Xiaoting He, Yuan Huang

Open access · goldAbstract read
In one paragraph

Article in BMC biology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
9.9field-weighted citation impact, top 2% 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

22 citing papers in PubMed, 44 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

10 authors at 3 institutions in 1 country.

Xuanzeng LiuCollege of Life Sciences, Shaanxi Normal University, Xi'an, China.
Muhammad MajidCollege of Life Sciences, Shaanxi Normal University, Xi'an, China.
Hao YuanSchool of Basic Medical Sciences, Xi'an Medical University, Xi'an, China.
Huihui ChangCollege of Life Science and Engineering, Henan University of Urban Construction, Pingdingshan, China.
Lina ZhaoCollege of Life Sciences, Shaanxi Normal University, Xi'an, China.
Yimeng NieCollege of Life Sciences, Shaanxi Normal University, Xi'an, China.
Lang HeCollege of Life Sciences, Shaanxi Normal University, Xi'an, China.
Xiaojing LiuCollege of Life Sciences, Shaanxi Normal University, Xi'an, China.
Xiaoting HeCollege of Life Sciences, Shaanxi Normal University, Xi'an, China.
Yuan HuangCollege of Life Sciences, Shaanxi Normal University, Xi'an, China. yuanh@snnu.edu.cn.ORCID 0000-0001-7683-9193
Shaanxi Normal University · CNHenan University of Urban Construction · CNXi'an Medical University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundTransposable elements (TEs) have been likened to parasites in the genome that reproduce and move ceaselessly in the host, continuously enlarging the host genome. However, the Piwi-interacting RNA (piRNA) pathway defends animal genomes against the harmful consequences of TE invasion by imposing small-RNA-mediated silencing. Here we compare the TE activity of two grasshopper species with different genome sizes in Acrididae (Locusta migratoria manilensis♀1C = 6.60 pg, Angaracris rhodopa♀1C = 16.36 pg) to ascertain the influence of piRNAs.

resultsWe discovered that repetitive sequences accounted for 74.56% of the genome in A. rhodopa, more than 56.83% in L. migratoria, and the large-genome grasshopper contained a higher TEs proportions. The comparative analysis revealed that 41 TEs (copy number > 500) were shared in both species. The two species exhibited distinct "landscapes" of TE divergence. The TEs outbreaks in the small-genome grasshopper occurred at more ancient times, while the large-genome grasshopper maintains active transposition events in the recent past. Evolutionary history studies on TEs suggest that TEs may be subject to different dynamics and resistances in these two species. We found that TE transcript abundance was higher in the large-genome grasshopper and the TE-derived piRNAs abundance was lower than in the small-genome grasshopper. In addition, we found that the piRNA methylase HENMT, which is underexpressed in the large-genome grasshopper, impedes the piRNA silencing to a lower level.

conclusionsOur study revealed that the abundance of piRNAs is lower in the gigantic genome grasshopper than in the small genome grasshopper. In addition, the key gene HENMT in the piRNA biogenesis pathway (Ping-Pong cycle) in the gigantic genome grasshopper is underexpressed. We hypothesize that low-level piRNA silencing unbalances the original positive correlation between TEs and piRNAs, and triggers TEs to proliferate out of control, which may be one of the reasons for the gigantism of grasshopper genomes.

Indexed as

GigantismGrasshoppersAnimalsDNA Transposable ElementsRNA InterferenceRNA, Small InterferingDNA Transposable ElementsRNA, Small InterferingGenome sizeGrasshopperpiRNA silencingTE transcriptsTransposable elements

Identifiers

PMID36307800
PMCPMC9615261
OpenAlexW4307511253

What Socratic holds

Textmetadata
LicenceCC BY
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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.