Evidence map›Paper›PMID 27317011›Full record

ArticleBMC plant biology2016

High-throughput development of simple sequence repeat markers for genetic diversity research in Crambe abyssinica.

Weicong Qi, Feng Lin, Yuhe Liu, Bangquan Huang, Jihua Cheng, Wei Zhang, Han Zhao

Abstract readEvaluation Study
In one paragraph

Article in BMC plant biology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing 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

18 citing papers in PubMed.

  1. Review
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  3. New Insights into Phylogenetic Relationship ofInternational journal of molecular sciences · 2023
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  4. Characteristics and Comparative Analysis of Seven Complete Plastomes ofInternational journal of molecular sciences · 2023
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  5. Development ofFrontiers in genetics · 2022
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  9. Complete Chloroplast Genomes ofPlants (Basel, Switzerland) · 2020
    Article
  10. Complete Chloroplast Genomes ofPlants (Basel, Switzerland) · 2019
    Article
  11. Article
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  13. Article
  14. Article
  15. Article
  16. Interspecific Divergence of TwoFrontiers in plant science · 2018
    Article
  17. Article
  18. Development of EST-SSR markers forApplications in plant sciences · 2017
    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

7 authors.

Weicong QiInstitute of Biotechnology, Provincial Key Laboratory of Agrobiology, Jiangsu Academy of Agricultural Sciences, Nanjing, 210014, China.
Feng LinInstitute of Biotechnology, Provincial Key Laboratory of Agrobiology, Jiangsu Academy of Agricultural Sciences, Nanjing, 210014, China.
Yuhe LiuDepartment of Crop Sciences, University of Illinois, Urbana-Champaign, IL, 61801, USA.
Bangquan HuangCollege of Life Science, Hubei University, Wuhan, 430062, China.
Jihua ChengCollege of Life Science, Hubei University, Wuhan, 430062, China.
Wei ZhangWaksman Institute of Microbiology, Rutgers University, 190 Frelinghuysen Road, Piscataway, NJ, 08854, USA.
Han ZhaoInstitute of Biotechnology, Provincial Key Laboratory of Agrobiology, Jiangsu Academy of Agricultural Sciences, Nanjing, 210014, China. zhaohan@jaas.ac.cn.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe allohexaploid Crambe abyssinica (crambe) is an oilseed crop that has been recognized for its potential value in the chemical industry, particularly in terms of producing high-erucic acid content vegetable oil. However, as an understudied crop, improvement of crambe has been hampered by the lack of genetic and genomic information to enhance its yield, oil quality and resistance against biotic and abiotic stress. Development of molecular markers is therefore of great significance to facilitate genetic improvement of crambe.

resultsIn this study, high-throughput sequencing was performed to generate sequences for the transcriptome and genome of a widely planted crambe cultivar, Galactica. A total of 186,778 expressed sequence tag (EST) contigs as 8,130,350 genomic contigs were assembled as well. Altogether, 82,523 pairs of primers were designed in the flanking sequences of the simple sequence repeat (SSR) within these contigs. Virtual PCR analysis showed that a fraction of these primers could be mapped onto the genomes of related species of Brassica, including Brassica rapa, B. oleraceae and B. napus. Genetic diversity analysis using a subset of 166 markers on 30 independent C. abyssinica accessions exhibited that 1) 95 % of the designed SSRs were polymorphic among these accessions; 2) the polymorphism information content (PIC) value of the markers ranged from 0.13 to 0.89; 3) the genetic distances (coefficient NEI72) between accessions varied from 0.06 to 0.36. Cluster analysis subsequent on the accessions demonstrated consistency with crambe breeding history. F-statistics analysis revealed a moderate level of genetic differentiation in C. abyssinica (Gst = 0.3934) and a accordingly low estimated gene flow (Nm = 0.7709).

conclusionApplication of high-throughput sequencing technology has facilitated SSR marker development, which was successfully employed in evaluating genetic diversity of C. abyssinica as demonstrated in our study. Results showed these molecular markers were robust and provided powerful tools for assessing genetic diversity and estimating crambe breeding history. Moreover, the SSR primers and sequence information developed in the study are freely available to the research community.

Indexed as

Genetic VariationMicrosatellite RepeatsBrassicaCrambe PlantExpressed Sequence TagsGenetic MarkersHigh-Throughput Nucleotide SequencingPolymorphism, GeneticGenetic MarkersCrambe abyssinicade novo assemblyEST-SSRGenetic diversityMolecular breedingNext-generation sequencingSSR

Identifiers

PMID27317011
PMCPMC4912734

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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.