Evidence map›Paper›PMID 31832922›Full record

ArticleActa parasitologica2020

The genomic survey of Tc1-like elements in the silkworm microsporidia Nosema bombycis.

Huali Song, Xiangyou Tang, Lan Lan, Xin Zhang, Xiaoyan Zhang

Abstract read
PubMed Publisher
In one paragraph

Article in Acta parasitologica, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
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

2 citing papers in PubMed.

  1. Article
  2. 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

5 authors.

Huali SongLaboratory of Animal Biology, Chongqing Normal University, Chongqing, 401331, China.
Xiangyou TangLaboratory of Animal Biology, Chongqing Normal University, Chongqing, 401331, China.
Lan LanLaboratory of Animal Biology, Chongqing Normal University, Chongqing, 401331, China.
Xin ZhangLaboratory of Animal Biology, Chongqing Normal University, Chongqing, 401331, China.
Xiaoyan ZhangLaboratory of Animal Biology, Chongqing Normal University, Chongqing, 401331, China. xyzhang18@163.com.ORCID http://orcid.org/0000-0002-6321-8600

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMicrosporidia Nosema bombycis is the destructive pathogen in the production of sericulture. The Tc1/mariner elements belong to important component of DNA transposon.

methodsThe genomic data of N. bombycis and related Nosema species were screened to identify the Tc1-like elements and analyzed the phylogenetic relationship, based on bioinformational analysis. High-throughput data of transcriptomes and small RNAs were used to evaluate the expressed level and potential rasiRNAs for the Tc1-like elements of N. bombycis.

resultsTwelve complete Tc1-like elements belonging to DD34,E clade is confirmed in the whole genome of N. bombycis, and divided into two branches. Six of them are sole in N. bombycis and thereby would be the molecular marker to differentiate this species from others Nosema spp. Most of the elements have the transcriptional active and are the source of sRNAs.

conclusionAbundant Tc1-like elements in N. bombycis reflect the expansion of transposons for this genomic characters, comparing with others Nosema spp. The finding of distribution, phylogeny and potential functional activity for Tc1Nbs in N. bombycis will help understanding the role of the DNA transposon in genomic evolution of microsporidia.

Indexed as

DNA Transposable ElementsGenome, FungalAnimalsBombyxGenomicsNosemaPhylogenyTranscriptomeDNA Transposable ElementsActiveGenomeMicrosporidiaNosema bombycisTc1-like

Identifiers

PMID31832922

What OpenQuestion holds

Textmetadata
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.