Evidence map›Paper›PMID 29703141›Full record

ArticleBMC genomics2018

Genome-wide identification and characterization of the SBP-box gene family in Petunia.

Qin Zhou, Sisi Zhang, Feng Chen, Baojun Liu, Lan Wu, Fei Li, Jiaqi Zhang, Manzhu Bao, Guofeng Liu

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 44 papers.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed
9.5field-weighted citation impact, top 2% 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

44 citing papers in PubMed, 98 citations in OpenAlex.

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  18. Review
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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

9 authors at 1 institution in 1 country.

Qin ZhouKey Laboratory of Horticultural Plant Biology, Ministry of Education; Key Laboratory of Urban Agriculture in Central China, Ministry of Agriculture; College of Horticulture and Forestry Sciences, Huazhong Agricultural University, Shizishan Street No. 1, Wuhan, 430070, China.
Sisi ZhangKey Laboratory of Horticultural Plant Biology, Ministry of Education; Key Laboratory of Urban Agriculture in Central China, Ministry of Agriculture; College of Horticulture and Forestry Sciences, Huazhong Agricultural University, Shizishan Street No. 1, Wuhan, 430070, China.
Feng ChenKey Laboratory of Horticultural Plant Biology, Ministry of Education; Key Laboratory of Urban Agriculture in Central China, Ministry of Agriculture; College of Horticulture and Forestry Sciences, Huazhong Agricultural University, Shizishan Street No. 1, Wuhan, 430070, China.
Baojun LiuKey Laboratory of Horticultural Plant Biology, Ministry of Education; Key Laboratory of Urban Agriculture in Central China, Ministry of Agriculture; College of Horticulture and Forestry Sciences, Huazhong Agricultural University, Shizishan Street No. 1, Wuhan, 430070, China.
Lan WuKey Laboratory of Horticultural Plant Biology, Ministry of Education; Key Laboratory of Urban Agriculture in Central China, Ministry of Agriculture; College of Horticulture and Forestry Sciences, Huazhong Agricultural University, Shizishan Street No. 1, Wuhan, 430070, China.
Fei LiKey Laboratory of Horticultural Plant Biology, Ministry of Education; Key Laboratory of Urban Agriculture in Central China, Ministry of Agriculture; College of Horticulture and Forestry Sciences, Huazhong Agricultural University, Shizishan Street No. 1, Wuhan, 430070, China.
Jiaqi ZhangKey Laboratory of Horticultural Plant Biology, Ministry of Education; Key Laboratory of Urban Agriculture in Central China, Ministry of Agriculture; College of Horticulture and Forestry Sciences, Huazhong Agricultural University, Shizishan Street No. 1, Wuhan, 430070, China.
Manzhu BaoKey Laboratory of Horticultural Plant Biology, Ministry of Education; Key Laboratory of Urban Agriculture in Central China, Ministry of Agriculture; College of Horticulture and Forestry Sciences, Huazhong Agricultural University, Shizishan Street No. 1, Wuhan, 430070, China.
Guofeng LiuKey Laboratory of Horticultural Plant Biology, Ministry of Education; Key Laboratory of Urban Agriculture in Central China, Ministry of Agriculture; College of Horticulture and Forestry Sciences, Huazhong Agricultural University, Shizishan Street No. 1, Wuhan, 430070, China. gfliu@mail.hzau.edu.cn.
Huazhong Agricultural University · CN

Funding

Ministry of Education of the People's Republic of China (CN) IRT13065National Natural Science Foundation of China 31772345National Natural Science Foundation of China 37471914
6 · The paper itself

Abstract

backgroundSQUAMOSA PROMOTER BINDING PROTEIN (SBP)-box genes encode a family of plant-specific transcription factors (TFs) that play important roles in many growth and development processes including phase transition, leaf initiation, shoot and inflorescence branching, fruit development and ripening etc. The SBP-box gene family has been identified and characterized in many species, but has not been well studied in Petunia, an important ornamental genus.

resultsWe identified 21 putative SPL genes of Petunia axillaris and P. inflata from the reference genome of P. axillaris N and P. inflata S6, respectively, which were supported by the transcriptome data. For further confirmation, all the 21 genes were also cloned from P. hybrida line W115 (Mitchel diploid). Phylogenetic analysis based on the highly conserved SBP domains arranged PhSPLs in eight groups, analogous to those from Arabidopsis and tomato. Furthermore, the Petunia SPL genes had similar exon-intron structure and the deduced proteins contained very similar conserved motifs within the same subgroup. Out of 21 PhSPL genes, fourteen were predicted to be potential targets of PhmiR156/157, and the putative miR156/157 response elements (MREs) were located in the coding region of group IV, V, VII and VIII genes, but in the 3'-UTR regions of group VI genes. SPL genes were also identified from another two wild Petunia species, P. integrifolia and P. exserta, based on their transcriptome databases to investigate the origin of PhSPLs. Phylogenetic analysis and multiple alignments of the coding sequences of PhSPLs and their orthologs from wild species indicated that PhSPLs were originated mainly from P. axillaris. qRT-PCR analysis demonstrated differential spatiotemperal expression patterns of PhSPL genes in petunia and many were expressed predominantly in the axillary buds and/or inflorescences. In addition, overexpression of PhSPL9a and PhSPL9b in Arabidopsis suggested that these genes play a conserved role in promoting the vegetative-to-reproductive phase transition.

conclusionPetunia genome contains at least 21 SPL genes, and most of the genes are expressed in different tissues. The PhSPL genes may play conserved and diverse roles in plant growth and development, including flowering regulation, leaf initiation, axillary bud and inflorescence development. This work provides a comprehensive understanding of the SBP-box gene family in Petunia and lays a significant foundation for future studies on the function and evolution of SPL genes in petunia.

Indexed as

Amino Acid MotifsAmino Acid SequenceConserved SequenceGene Expression ProfilingGene Expression Regulation, PlantGenome, PlantMultigene FamilyPetuniaPhylogenyPlant ProteinsSequence Analysis, RNATissue DistributionTranscription FactorsPlant ProteinsTranscription FactorsExpression patternsFloweringmiR156/miR157PetuniaSPL genesTranscription factor

Identifiers

PMID29703141
PMCPMC6389188
OpenAlexW2790822321

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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.