Evidence map›Paper›PMID 34425748›Full record

ArticleBMC plant biology2021

Comparative phylogenetic analysis of CBL reveals the gene family evolution and functional divergence in Saccharum spontaneum.

Xiaomin Feng, Yongjun Wang, Nannan Zhang, Shuai Gao, Jiayun Wu, Rui Liu, Yonghong Huang, Jisen Zhang, Yongwen Qi

Open access · goldAbstract readComparative Study
In one paragraph

Article in BMC plant biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
8.0field-weighted citation impact, top 3% 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

9 citing papers in PubMed, 21 citations in OpenAlex.

  1. Genome-Wide Identification and Characterisation of theInternational journal of molecular sciences · 2025
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  6. Genome-wide discovery of CBL genes inForestry research · 2023
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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 3 institutions in 1 country.

Xiaomin Feng *Guangdong Sugarcane Genetic Improvement Engineering Center, Institute of Nanfan & Seed Industry, Guangdong Academy of Sciences, Room 1909, Biological Engineering Building, Jianghai Avenue, Haizhu District, Guangzhou, 510316, Guangdong Province, China.
Yongjun Wang *Center for Genomics and Biotechnology, Fujian Provincial Key Laboratory of Haixia Applied Plant Systems Biology, College of Agriculture, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.
Nannan ZhangGuangdong Sugarcane Genetic Improvement Engineering Center, Institute of Nanfan & Seed Industry, Guangdong Academy of Sciences, Room 1909, Biological Engineering Building, Jianghai Avenue, Haizhu District, Guangzhou, 510316, Guangdong Province, China.
Shuai GaoGuangdong Sugarcane Genetic Improvement Engineering Center, Institute of Nanfan & Seed Industry, Guangdong Academy of Sciences, Room 1909, Biological Engineering Building, Jianghai Avenue, Haizhu District, Guangzhou, 510316, Guangdong Province, China.
Jiayun WuGuangdong Sugarcane Genetic Improvement Engineering Center, Institute of Nanfan & Seed Industry, Guangdong Academy of Sciences, Room 1909, Biological Engineering Building, Jianghai Avenue, Haizhu District, Guangzhou, 510316, Guangdong Province, China.
Rui LiuGuangdong Sugarcane Genetic Improvement Engineering Center, Institute of Nanfan & Seed Industry, Guangdong Academy of Sciences, Room 1909, Biological Engineering Building, Jianghai Avenue, Haizhu District, Guangzhou, 510316, Guangdong Province, China.
Yonghong HuangGuangdong Sugarcane Genetic Improvement Engineering Center, Institute of Nanfan & Seed Industry, Guangdong Academy of Sciences, Room 1909, Biological Engineering Building, Jianghai Avenue, Haizhu District, Guangzhou, 510316, Guangdong Province, China.
Jisen ZhangCenter for Genomics and Biotechnology, Fujian Provincial Key Laboratory of Haixia Applied Plant Systems Biology, College of Agriculture, Fujian Agriculture and Forestry University, Fuzhou, 350002, China.
Yongwen QiGuangdong Sugarcane Genetic Improvement Engineering Center, Institute of Nanfan & Seed Industry, Guangdong Academy of Sciences, Room 1909, Biological Engineering Building, Jianghai Avenue, Haizhu District, Guangzhou, 510316, Guangdong Province, China. yongwen2001@126.com.
Guangdong Academy of Sciences · CNFujian Agriculture and Forestry University · CNGuangxi Academy of Agricultural Science · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe identification and functional analysis of genes that improve tolerance to low potassium stress in S. spontaneum is crucial for breeding sugarcane cultivars with efficient potassium utilization. Calcineurin B-like (CBL) protein is a calcium sensor that interacts with specific CBL-interacting protein kinases (CIPKs) upon plants' exposure to various abiotic stresses.

resultsIn this study, nine CBL genes were identified from S. spontaneum. Phylogenetic analysis of 113 CBLs from 13 representative plants showed gene expansion and strong purifying selection in the CBL family. Analysis of CBL expression patterns revealed that SsCBL01 was the most commonly expressed gene in various tissues at different developmental stages. Expression analysis of SsCBLs under low K

conclusionsThis study provided insights into the evolution of the CBL gene family and preliminarily demonstrated that the plasma membrane protein SsCBL01 was involved in the response to low K

Indexed as

Genome, PlantPhylogenyCalcineurinCell MembraneCrops, AgriculturalEvolution, MolecularGene Expression Regulation, PlantGenetic VariationPlant ImmunityPlant ProteinsPotassium DeficiencySaccharumSequence Analysis, ProteinCalcineurinPlant ProteinsCBLEvolutionGene expressionLow K+ stressS. spontaneum

Identifiers

PMID34425748
PMCPMC8383383
OpenAlexW3195287799

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