4.8 Article

Chromatin and regulatory differentiation between bundle sheath and mesophyll cells in maize

期刊

PLANT JOURNAL
卷 109, 期 3, 页码 675-692

出版社

WILEY
DOI: 10.1111/tpj.15586

关键词

C-4 photosynthesis; Zea mays; bundle sheath; mesophyll; transcriptional regulation

资金

  1. National Science Foundation of China [92035302, 31871313]
  2. Agricultural Science and Technology Innovation Program [CAASZDXT2019003]
  3. Hong Kong General Research Fund (GRF) [14104119, AoE/M-403/16]
  4. Natural Science Foundation of China (NSFC) [32100438]
  5. China Postdoctoral Science Foundation [2020M672858, 2021T140677]

向作者/读者索取更多资源

Through analyzing BS and M cells isolated from maize leaves using multiple techniques, it was found that chromatin accessibility coordinates with epigenetic features to regulate gene expression, and the preferential expression of genes in specific cell types is finely tuned by multiple chromatin features. This coordination is critical in ensuring the cell type-specific function of key C-4 genes.
C-4 plants partition photosynthesis enzymes between the bundle sheath (BS) and the mesophyll (M) cells for the better delivery of CO2 to RuBisCO and to reduce photorespiration. To better understand how C-4 photosynthesis is regulated at the transcriptional level, we performed RNA-seq, ATAC-seq, ChIP-seq and Bisulfite-seq (BS-seq) on BS and M cells isolated from maize leaves. By integrating differentially expressed genes with chromatin features, we found that chromatin accessibility coordinates with epigenetic features, especially H3K27me3 modification and CHH methylation, to regulate cell type-preferentially enriched gene expression. Not only the chromatin-accessible regions (ACRs) proximal to the genes (pACRs) but also the distal ACRs (dACRs) are determinants of cell type-preferentially enriched expression. We further identified cell type-preferentially enriched motifs, e.g. AAAG for BS cells and TGACC/T for M cells, and determined their corresponding transcription factors: DOFs and WRKYs. The complex interaction between cis and trans factors in the preferential expression of C-4 genes was also observed. Interestingly, cell type-preferentially enriched gene expression can be fine-tuned by the coordination of multiple chromatin features. Such coordination may be critical in ensuring the cell type-specific function of key C-4 genes. Based on the observed cell type-preferentially enriched expression pattern and coordinated chromatin features, we predicted a set of functionally unknown genes, e.g. Zm00001d042050 and Zm00001d040659, to be potential key C-4 genes. Our findings provide deep insight into the architectures associated with C-4 gene expression and could serve as a valuable resource to further identify the regulatory mechanisms present in C-4 species.

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