Evidence map›Paper›PMID 40011803›Full record

ArticleBMC plant biology2025

Transcriptomic analysis offers deep insights into the Increased Grain Length 1 (IGL1) regulation of grain length.

Liran Sang, Ending Xu, Yan Liu, Tiange Hu, Mengqi Yang, Jiayu Niu, Chong Lu, Yi Zhou, Yifei Sun, Zhaoyu Zhai and 5 more

Erratum issuedAbstract read
In one paragraph

Article in BMC plant biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 1 paper.

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0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

15 authors.

Liran Sang *College of Life Sciences, Nanjing Agricultural University, Nanjing , Jiangsu, 210095, China.
Ending Xu *Anhui Province Key Laboratory of Rice Genetics and Breeding, Rice Research Institute, Anhui Academy of Agricultural Sciences, Hefei, Anhui, 230041, China.
Yan Liu *College of Life Sciences, Nanjing Agricultural University, Nanjing , Jiangsu, 210095, China.
Tiange Hu *College of Life Sciences, Nanjing Agricultural University, Nanjing , Jiangsu, 210095, China.
Mengqi YangCollege of Life Sciences, Nanjing Agricultural University, Nanjing , Jiangsu, 210095, China.
Jiayu NiuCollege of Life Sciences, Nanjing Agricultural University, Nanjing , Jiangsu, 210095, China.
Chong LuCollege of Life Sciences, Nanjing Agricultural University, Nanjing , Jiangsu, 210095, China.
Yi ZhouCollege of Life Sciences, Nanjing Agricultural University, Nanjing , Jiangsu, 210095, China.
Yifei SunCollege of Life Sciences, Nanjing Agricultural University, Nanjing , Jiangsu, 210095, China.
Zhaoyu ZhaiCollege of Artificial Intelligence, Nanjing Agricultural University, Nanjing, 210095, China.
Dina AbdulmajidRice Research and Training Centre, Field Crops Research Institute, A.R.C, Sakha, Kafrelsheikh, 33717, Egypt.
Peijiang ZhangAnhui Province Key Laboratory of Rice Genetics and Breeding, Rice Research Institute, Anhui Academy of Agricultural Sciences, Hefei, Anhui, 230041, China.
Qianqian WangCollege of Life Sciences, Nanjing Agricultural University, Nanjing , Jiangsu, 210095, China. 18761869832@163.com.
Honggui LaCollege of Life Sciences, Nanjing Agricultural University, Nanjing , Jiangsu, 210095, China. hongguila@njau.edu.cn.
Yu ZouAnhui Province Key Laboratory of Rice Genetics and Breeding, Rice Research Institute, Anhui Academy of Agricultural Sciences, Hefei, Anhui, 230041, China. zouyu@aaas.org.cn.

Funding

Jiangsu Agriculture Science and Technology Innovation Fund (JASTIF) CX(22)3156Open Research Fund Program of Anhui Province Key Laboratory of Rice Genetics and Breeding SDKF-2023-04
6 · The paper itself

Abstract

backgroundAlthough great progress has been made in recent years in identifying novel genes or natural alleles for rice yield improvement, the molecular mechanisms of how these genes/natural alleles regulate yield-associated traits, such as grain length and 1000-grain weight, remain largely unclear. An in-depth understanding of the roles of these genes/natural alleles in controlling yield traits become a necessity to ultimately increase rice yield via novel molecular techniques, such as gene editing.

resultsIn this study, the roles of IGL1, which was previously identified through a map-based cloning approach, in the regulation of grain length were investigated by overexpressing and knocking out it in the Nipponbare genetic background. Overexpression and knockout of IGL1 (the resulting transgenic lines were hereafter designated IGL1-OE and IGL1-CR lines, respectively) led to elongation and shortening of grains, respectively. To further elucidate the molecular mechanisms behind the IGL1 action, young panicles from IGL1-OE and IGL1-CR lines were subjected to mRNA sequencing. The results showed that both overexpression and knockout of IGL1 all resulted in a large number of upregulated and downregulated differentially expression genes (DEGs) relative to wild-type NPB control lines. A total of 984 DEGs overlapped between upregulated DEGs from IGL1-OE and downregulated DEGs from IGL1-CR; 1146 DEGs were common to downregulated DEGs from IGL1-OE and upregulated DEGs from IGL1-CR. GO term and KEGG pathway analysis revealed that IGL1-upregulated DEGs were associated with extracellular region, protein ubiquitination, cell-wall modification, BR signaling, cell cycle, etc.; by comparison, the IGL1-downregulated DEGs were connected with extracellular region, response to wounding, flavonoid biosynthesis, jasmonic-acid signaling, glucose/sucrose metabolism, etc. Some phytohormone-associated genes (like OsYUCCA4, OsPIN10b, OsBAK1, and OsDLT), TF genes (like OsMADS1 and OsGASR9), grain length-regulating genes (like An-1, GS9, OsIQD14, and TGW2) showed significant upregulation or downregulation in IGL1-OE or IGL1-CR.

conclusionOur result clearly demonstrated that IGL1 is an important regulator of grain length, and has profound impacts on genome-wide gene expression, suggesting that it may work together with certain TFs. Overexpression or knockout of IGL1 appears to cause complex expression changes of genes associated with phytohormones, TFs, grain length-regulating factors, which ultimately brings about the grain elongation.

Indexed as

Gene Expression Regulation, PlantOryzaPlant ProteinsGene Expression ProfilingGenes, PlantLife History TraitsPlants, Genetically ModifiedReal-Time Polymerase Chain ReactionTranscriptomePlant ProteinsDifferentially expressed gene (DEG)Grain lengthIGL1MRNA sequencing (mRNA-seq)PhytohormoneTranscription factor (TF)

Identifiers

PMID40011803
PMCPMC11866874

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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.