Evidence map›Paper›PMID 31034501›Full record

ArticlePloS one2019

Transcriptome analysis and annotation: SNPs identified from single copy annotated unigenes of three polyploid blueberry crops.

Yunsheng Wang, Muhammad Qasim Shahid, Fozia Ghouri, Sezai Ercişli, Faheem Shehzad Baloch, Fei Nie

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Article in PloS one, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

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0cells of the map it votes in
5citing papers in PubMed
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1 · What the graph read from it

What it found

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3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Yunsheng WangCollege of Life and Health Science, Kaili University, Kaili City, Guizhou Province, China.ORCID 0000-0002-0595-5661
Muhammad Qasim ShahidState Key Laboratory for Conservation and Utilization of Subtropical Agro-Bioresources, South China Agricultural University, Guangzhou, China.
Fozia GhouriState Key Laboratory for Conservation and Utilization of Subtropical Agro-Bioresources, South China Agricultural University, Guangzhou, China.
Sezai ErcişliDepartment of Horticulture, Faculty of Agriculture, Ataturk University, Erzurum, Turkey.
Faheem Shehzad BalochDepartment of Field Crops, Faculty of Agricultural and Natural Sciences, Abant İzzet Baysal University, Bolu, Turkey.
Fei NieBiological Institute of Guizhou Province, Guiyang City, Guizhou Province, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Blueberry is a kind of new rising popular perennial fruit with high healthful quality. It is of utmost importance to develop new blueberry varieties for different climatic zones to satisfy the demand of people in the world. Molecular marker assisted breeding is believed to be an ideal method for the development of new blueberry varieties for its shorter breeding cycle than the conventional breeding. Simple sequence repeats (SSRs) and single nucleotide polymorphisms (SNPs) markers are widely used molecular tools for marker assisted breeding, which could be detected at large scale by the transcriptome sequencing. Here, we sequenced the leaves transcriptome of 19 rabbiteye (Vaccinium ashei Reade), 13 southern highbush (Vaccinium. corymbosum L × native southern Vaccinium Spp) and 22 cultivars of northern highbush blueberry (Vaccinium corymbosum L) by using next generation sequencing technologies. A total of 80.825 Gb clean data with an average of about 12.525 million reads per cultivar were obtained. We assembled 58,968, 55,973 and 53,887 unigenes by using the clean data from rabbiteye, southern highbush and northern highbush blueberry cultivars, respectively. Among these unigenes, 3599, 3495 and 3513 unigenes were detected as candidate resistance genes in three blueberry crops. Moreover, we identified more than 8756, 9020, and 9198 SSR markers from these unigenes, and 7665, 4861, 13,063 SNPs from the annotated single copy unigenes, respectively. The results will be helpful for the molecular genetics and association analysis of blueberry and the basic molecular information of pest and disease resistance of blueberry, and would also offer huge number of molecular tools for the marker assisted breeding to produce blueberry cultivars with different adaptive characteristics.

Indexed as

Gene DosageGene Expression ProfilingGenes, PlantMolecular Sequence AnnotationPolyploidyBlueberry PlantsGene Expression Regulation, PlantGene FrequencyGenetic MarkersHeterozygoteMicrosatellite RepeatsPolymorphism, Single NucleotideTranscriptomeGenetic Markers

Identifiers

PMID31034501
PMCPMC6488077

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