Comparative Transcriptomic Analysis of Gossypium hirsutum Fiber Development in Mutant Materials (xin w 139) Provides New Insights into Cotton Fiber Development

被引:3
|
作者
Li, Chunping [1 ]
Zhao, Jieyin [2 ]
Liu, Zhongshan [1 ]
Yang, Yanlong [1 ]
Lai, Chengxia [1 ]
Ma, Jun [1 ]
Aierxi, Alifu [1 ]
机构
[1] Xinjiang Acad Agr Sci, Res Inst Econ Crops, Urumqi 830091, Peoples R China
[2] Xinjiang Agr Univ, Coll Agr, Engn Res Ctr Cotton, Minist Educ, 311 Nongda East Rd, Urumqi 830052, Peoples R China
来源
PLANTS-BASEL | 2024年 / 13卷 / 08期
关键词
Gossypium hirsutum; mutant; fiber development; RNA-seq; candidate genes; CELL ELONGATION; GENE; GENOME;
D O I
10.3390/plants13081127
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Cotton is the most widely planted fiber crop in the world, and improving cotton fiber quality has long been a research hotspot. The development of cotton fibers is a complex process that includes four consecutive and overlapping stages, and although many studies on cotton fiber development have been reported, most of the studies have been based on cultivars that are promoted in production or based on lines that are used in breeding. Here, we report a phenotypic evaluation of Gossypium hirsutum based on immature fiber mutant (xin w 139) and wild-type (Xin W 139) lines and a comparative transcriptomic study at seven time points during fiber development. The results of the two-year study showed that the fiber length, fiber strength, single-boll weight and lint percentage of xin w 139 were significantly lower than those of Xin W 139, and there were no significant differences in the other traits. Principal component analysis (PCA) and cluster analysis of the RNA-sequencing (RNA-seq) data revealed that these seven time points could be clearly divided into three different groups corresponding to the initiation, elongation and secondary cell wall (SCW) synthesis stages of fiber development, and the differences in fiber development between the two lines were mainly due to developmental differences after twenty days post anthesis (DPA). Differential expression analysis revealed a total of 5131 unique differentially expressed genes (DEGs), including 290 transcription factors (TFs), between the 2 lines. These DEGs were divided into five clusters. Each cluster functional category was annotated based on the KEGG database, and different clusters could describe different stages of fiber development. In addition, we constructed a gene regulatory network by weighted correlation network analysis (WGCNA) and identified 15 key genes that determined the differences in fiber development between the 2 lines. We also screened seven candidate genes related to cotton fiber development through comparative sequence analysis and qRT-PCR; these genes included three TFs (GH_A08G1821 (bHLH), GH_D05G3074 (Dof), and GH_D13G0161 (C3H)). These results provide a theoretical basis for obtaining an in-depth understanding of the molecular mechanism of cotton fiber development and provide new genetic resources for cotton fiber research.
引用
收藏
页数:17
相关论文
共 43 条
  • [31] Molecular cloning and characterization of GhAPm, a gene encoding the μ subunit of the clathrin-associated adaptor protein complex that is associated with cotton (Gossypium hirsutum) fiber development
    Tao Zhou
    Rui Zhang
    Dawei Yang
    Sandui Guo
    Molecular Biology Reports, 2011, 38 : 3309 - 3317
  • [32] A Novel Tandem Zinc Finger Protein in Gossypium hirsutum, GhTZF2, Interacts with GhMORF8 to Regulate Cotton Fiber Cell Development
    Li, Yang
    Xi, Wei
    Hao, Jianfeng
    Zhang, Li
    Wen, Xingpeng
    Wu, Zhiguo
    Zhu, Yuxian
    AGRONOMY-BASEL, 2023, 13 (02):
  • [33] Molecular cloning and characterization of GhAPm, a gene encoding the μ subunit of the clathrin-associated adaptor protein complex that is associated with cotton (Gossypium hirsutum) fiber development
    Zhou, Tao
    Zhang, Rui
    Yang, Dawei
    Guo, Sandui
    MOLECULAR BIOLOGY REPORTS, 2011, 38 (05) : 3309 - 3317
  • [34] Comparative phosphoproteomic analysis of BR-defective mutant reveals a key role of GhSK13 in regulating cotton fiber development
    Lingling Wang
    Han Cheng
    Fangjie Xiong
    Shuya Ma
    Lei Zheng
    Yun Song
    Kexuan Deng
    Huanhuan Wu
    Fuguang Li
    Zuoren Yang
    Science China Life Sciences, 2020, 63 : 1905 - 1917
  • [35] Genome-wide analysis reveals rapid and dynamic changes in miRNA and siRNA sequence and expression during ovule and fiber development in allotetraploid cotton (Gossypium hirsutum L.)
    Mingxiong Pang
    Andrew W Woodward
    Vikram Agarwal
    Xueying Guan
    Misook Ha
    Vanitharani Ramachandran
    Xuemei Chen
    Barbara A Triplett
    David M Stelly
    Z Jeffrey Chen
    Genome Biology, 10
  • [36] Genome-wide investigation and expression profiling of APX gene family in Gossypium hirsutum provide new insights in redox homeostasis maintenance during different fiber development stages
    Tao, Chengcheng
    Jin, Xiang
    Zhu, Liping
    Xie, Quanliang
    Wang, Xuchu
    Li, Hongbin
    MOLECULAR GENETICS AND GENOMICS, 2018, 293 (03) : 685 - 697
  • [37] Genome-wide analysis of gene expression of EMS-induced short fiber mutant Ligon lintless-y (liy) in cotton (Gossypium hirsutum L.)
    Naoumkina, Marina
    Bechere, Efrem
    Fang, David D.
    Thyssen, Gregory N.
    Florane, Christopher B.
    GENOMICS, 2017, 109 (3-4) : 320 - 329
  • [38] Gene expression profile analysis of Ligon lintless-1 (Li1) mutant reveals important genes and pathways in cotton leaf and fiber development
    Ding, Mingquan
    Jiang, Yurong
    Cao, Yuefen
    Lin, Lifeng
    He, Shae
    Zhou, Wei
    Rong, Junkang
    GENE, 2014, 535 (02) : 273 - 285
  • [39] GhH2A12, a replication-dependent histone H2A gene from Gossypium hirsutum, is negatively involved in the development of cotton fiber cells
    Hao, Juan
    Chen, Sheng
    Tu, Lili
    Hu, Haiyan
    Zhang, Xianlong
    PLANT CELL REPORTS, 2014, 33 (10) : 1711 - 1721
  • [40] GhH2A12, a replication-dependent histone H2A gene from Gossypium hirsutum, is negatively involved in the development of cotton fiber cells
    Juan Hao
    Sheng Chen
    Lili Tu
    Haiyan Hu
    Xianlong Zhang
    Plant Cell Reports, 2014, 33 : 1711 - 1721