Evidence map›Paper›PMID 26779288›Full record

ArticleMobile DNA2016

Isolation and characterization of putative functional long terminal repeat retrotransposons in the Pyrus genome.

Shuang Jiang, Danying Cai, Yongwang Sun, Yuanwen Teng

Open access · goldAbstract read
In one paragraph

Article in Mobile DNA, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
4.1field-weighted citation impact, top 7% 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

5 citing papers in PubMed, 15 citations in OpenAlex.

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  5. Mobile DNA · 2017
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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

4 authors at 2 institutions in 1 country.

Shuang JiangDepartment of Horticulture, Zhejiang University, Hangzhou, Zhejiang 310058 China ; Forest & Fruit Tree Institute, Shanghai Academy of Agricultural Sciences, Shanghai, 201403 China.
Danying CaiInstitute of Horticulture, Zhejiang Academy of Agricultural Sciences, Hangzhou, Zhejiang 310021 China.
Yongwang SunDepartment of Horticulture, Zhejiang University, Hangzhou, Zhejiang 310058 China ; The Key Laboratory of Horticultural Plant Growth, Development and Quality Improvement, The Ministry of Agriculture of China, Hangzhou, Zhejiang 310058 China ; Zhejiang Provincial Key Laboratory of Horticultural Plant Integrative Biology, Hangzhou, Zhejiang 310058 China.
Yuanwen TengDepartment of Horticulture, Zhejiang University, Hangzhou, Zhejiang 310058 China ; The Key Laboratory of Horticultural Plant Growth, Development and Quality Improvement, The Ministry of Agriculture of China, Hangzhou, Zhejiang 310058 China ; Zhejiang Provincial Key Laboratory of Horticultural Plant Integrative Biology, Hangzhou, Zhejiang 310058 China.
Zhejiang University · CNZheJiang Academy of Agricultural Sciences · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundLong terminal repeat (LTR)-retrotransposons constitute 42.4 % of the genome of the 'Suli' pear (Pyrus pyrifolia white pear group), implying that retrotransposons have played important roles in Pyrus evolution. Therefore, further analysis of retrotransposons will enhance our understanding of the evolutionary history of Pyrus.

resultsWe identified 1836 LTR-retrotransposons in the 'Suli' pear genome, of which 440 LTR-retrotransposons were predicted to contain at least two of three gene models (gag, integrase and reverse transcriptase). Because these were most likely to be functional transposons, we focused our analyses on this set of 440. Most of the LTR-retrotransposons were estimated to have inserted into the genome less than 2.5 million years ago. Sequence analysis showed that the reverse transcriptase component of the identified LTR-retrotransposons was highly heterogeneous. Analyses of transcripts assembled from RNA-Seq databases of two cultivars of Pyrus species showed that LTR-retrotransposons were expressed in the buds and fruit of Pyrus. A total of 734 coding sequences in the 'Suli' genome were disrupted by the identified LTR-retrotransposons. Five high-copy-number LTR-retrotransposon families were identified in Pyrus. These families were rarely found in the genomes of Malus and Prunus, but were distributed extensively in Pyrus and abundance varied between species.

conclusionsWe identified potentially functional, full-length LTR-retrotransposons with three gene models in the 'Suli' genome. The analysis of RNA-seq data demonstrated that these retrotransposons are expressed in the organs of pears. The differential copy number of LTR-retrotransposon families between Pyrus species suggests that the transposition of retrotransposons is an important evolutionary force driving the genetic divergence of species within the genus.

Indexed as

DistributionGenetic diversityInsertion timePyrusRetrotransposons

Identifiers

PMID26779288
PMCPMC4715297
OpenAlexW2280873042

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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.