4.6 Article

Single-Cell Transcriptome and Network Analyses Unveil Key Transcription Factors Regulating Mesophyll Cell Development in Maize

期刊

GENES
卷 13, 期 2, 页码 -

出版社

MDPI
DOI: 10.3390/genes13020374

关键词

scRNA-seq; M-cell development; pseudo-time analysis; coexpression and regulatory network; transcript factor; maize

资金

  1. National Key Research and Development Program of China [2020YFE0202900]
  2. National Natural Science Foundation of China [32070561, U20A2030]
  3. Postgraduate Research & Practice Innovation Program of Jiangsu Province [KYCX18_0644]
  4. State Key Laboratory of Crop Genetics and Germplasm Enhancement [ZW202001]
  5. National Transgenic Major Project [2018ZX08020-003]
  6. Jiangsu Province Government Project [BM2018003]
  7. Open Foundation of Jiangsu Key Laboratory of Crop Genomics and Molecular Breeding [PL201801]

向作者/读者索取更多资源

This study reveals the involvement of several transcription factor families, including HSF and COL, in the regulation of maize mesophyll cell development at different stages, with the involvement of epigenetic regulation.
Background: Maize mesophyll (M) cells play important roles in various biological processes such as photosynthesis II and secondary metabolism. Functional differentiation occurs during M-cell development, but the underlying mechanisms for regulating M-cell development are largely unknown. Results: We conducted single-cell RNA sequencing (scRNA-seq) to profile transcripts in maize leaves. We then identified coregulated modules by analyzing the resulting pseudo-time-series data through gene regulatory network analyses. WRKY, ERF, NAC, MYB and Heat stress transcription factor (HSF) families were highly expressed in the early stage, whereas CONSTANS (CO)-like (COL) and ERF families were highly expressed in the late stage of M-cell development. Construction of regulatory networks revealed that these transcript factor (TF) families, especially HSF and COL, were the major players in the early and later stages of M-cell development, respectively. Integration of scRNA expression matrix with TF ChIP-seq and Hi-C further revealed regulatory interactions between these TFs and their targets. HSF1 and COL8 were primarily expressed in the leaf bases and tips, respectively, and their targets were validated with protoplast-based ChIP-qPCR, with the binding sites of HSF1 being experimentally confirmed. Conclusions: Our study provides evidence that several TF families, with the involvement of epigenetic regulation, play vital roles in the regulation of M-cell development in maize.

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