Evidence map›Paper›PMID 29499648›Full record

ArticleBMC genomics2018

Genome-wide identification, phylogeny, evolution, and expression patterns of MtN3/saliva/SWEET genes and functional analysis of BcNS in Brassica rapa.

Liming Miao, Yanxia Lv, Lijun Kong, Qizhen Chen, Chaoquan Chen, Jia Li, Fanhuan Zeng, Shenyun Wang, Jianbin Li, Li Huang and 2 more

Open access · goldAbstract read
In one paragraph

Article in BMC genomics, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

14 citing papers in PubMed, 30 citations in OpenAlex.

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  12. Plants (Basel, Switzerland) · 2019
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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

12 authors at 4 institutions in 2 countries.

Liming MiaoLaboratory of Cell and Molecular Biology, Institute of Vegetable Science, Zhejiang University, 866 Yuhangtang Road, Zhejiang Province, Hangzhou, 310058, P. R. China.
Yanxia LvLaboratory of Cell and Molecular Biology, Institute of Vegetable Science, Zhejiang University, 866 Yuhangtang Road, Zhejiang Province, Hangzhou, 310058, P. R. China.
Lijun KongLaboratory of Cell and Molecular Biology, Institute of Vegetable Science, Zhejiang University, 866 Yuhangtang Road, Zhejiang Province, Hangzhou, 310058, P. R. China.
Qizhen ChenLaboratory of Cell and Molecular Biology, Institute of Vegetable Science, Zhejiang University, 866 Yuhangtang Road, Zhejiang Province, Hangzhou, 310058, P. R. China.
Chaoquan ChenLaboratory of Cell and Molecular Biology, Institute of Vegetable Science, Zhejiang University, 866 Yuhangtang Road, Zhejiang Province, Hangzhou, 310058, P. R. China.
Jia LiLaboratory of Cell and Molecular Biology, Institute of Vegetable Science, Zhejiang University, 866 Yuhangtang Road, Zhejiang Province, Hangzhou, 310058, P. R. China.
Fanhuan ZengLaboratory of Cell and Molecular Biology, Institute of Vegetable Science, Zhejiang University, 866 Yuhangtang Road, Zhejiang Province, Hangzhou, 310058, P. R. China.
Shenyun WangInstitute of Vegetable Science, Jiangsu Academy of Agricultural Sciences, Nanjing, 210014, P. R. China.
Jianbin LiInstitute of Vegetable Science, Jiangsu Academy of Agricultural Sciences, Nanjing, 210014, P. R. China.
Li HuangLaboratory of Cell and Molecular Biology, Institute of Vegetable Science, Zhejiang University, 866 Yuhangtang Road, Zhejiang Province, Hangzhou, 310058, P. R. China.
Jiashu CaoLaboratory of Cell and Molecular Biology, Institute of Vegetable Science, Zhejiang University, 866 Yuhangtang Road, Zhejiang Province, Hangzhou, 310058, P. R. China.
Xiaolin YuLaboratory of Cell and Molecular Biology, Institute of Vegetable Science, Zhejiang University, 866 Yuhangtang Road, Zhejiang Province, Hangzhou, 310058, P. R. China. xlyu@zju.edu.cn.
Horticultural Research Institute · USZhejiang University · CNJiangsu Academy of Agricultural Sciences · CNNanjing Agricultural University · CN

Funding

Ministry of Agriculture of the People's Republic of China 2014-Z28Ministry of Science and Technology of the People's Republic of China 2016YFD0100204-31National Natural Science Foundation of China 31460521Science and Technology Department of Jiangsu Province CX(15)1016Science Thchnology Department of Zhejiang Province 2014C32008Science Thchnology Department of Zhejiang Province 2016C02051-6-1
6 · The paper itself

Abstract

backgroundMembers of the MtN3/saliva/SWEET gene family are present in various organisms and are highly conserved. Their precise biochemical functions remain unclear, especially in Chinese cabbage. Based on the whole genome sequence, this study aims to identify the MtN3/saliva/SWEETs family members in Chinese cabbage and to analyze their classification, gene structure, chromosome distribution, phylogenetic relationship, expression pattern, and biological functions.

resultsWe identified 34 SWEET genes in Chinese cabbage and analyzed their localization on chromosomes and transmembrane regions of their corresponding proteins. Analysis of a phylogenetic tree indicated that there were at least 17 supposed ancestor genes before the separation in Brassica rapa and Arabidopsis. The expression patterns of these genes in different tissues and flower developmental stages of Chinese cabbage showed that they are mainly involved in reproductive development. The Ka/Ks ratio between paralogous SWEET gene pairs of B. rapa were far less than 1. In our previous study, At2g39060 homologous gene Bra000116 (BraSWEET9, also named BcNS, Brassica Nectary and Stamen) played an important role during flower development in Chinese cabbage. Instantaneous expression experiments in onion epidermal cells showed that the gene encoding this protein is localized to the plasma membrane. A basal nectary split is the phenotype of transgenic plants transformed with the antisense expression vector.

conclusionThis study is the first to perform a sequence analysis, structures analysis, physiological and biochemical characteristics analysis of the MtN3/saliva/SWEETs gene in Chinese cabbage and to verify the function of BcNS. A total of 34 SWEET genes were identified and they are distributed among ten chromosomes and one scaffold. The Ka/Ks ratio implies that the duplication genes suffered strong purifying selection for retention. These genes were differentially expressed in different floral organs. The phenotypes of the transgenic plants indicated that BcNs participates in the development of the floral nectary. This study provides a basis for further functional analysis of the MtN3/saliva/SWEETs gene family.

Indexed as

Evolution, MolecularGene Expression Regulation, PlantGenome, PlantBrassica rapaChromosome MappingChromosomes, PlantFlowersGene Expression Regulation, DevelopmentalMembrane ProteinsPhylogenyPlant ProteinsWhole Genome SequencingMembrane ProteinsnodulinPlant ProteinsBcNSChinese cabbage (Brassica rapa syn. Brassica campestris)Functional analysisGene familyMtN3/saliva/SWEETsNectary

Identifiers

PMID29499648
PMCPMC5834901
OpenAlexW2794531097

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LicenceCC BY
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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.