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DNA 甲基化与转录组关联分析鉴定 BpCYCD3;2 为影响同源四倍体白桦(Betula pendula)叶片细胞分裂的参与者。

The association analysis of DNA methylation and transcriptomics identified BpCYCD3;2 as a participant in influencing cell division in autotetraploid birch (Betula pendula) leaves.

机构信息

State Key Laboratory of Tree Genetics and Breeding, Northeast Forestry University, 26 Hexing Road, Harbin 150040, China.

State Key Laboratory of Tree Genetics and Breeding, Northeast Forestry University, 26 Hexing Road, Harbin 150040, China.

出版信息

Plant Sci. 2024 Jul;344:112099. doi: 10.1016/j.plantsci.2024.112099. Epub 2024 Apr 17.

Abstract

Polyploidization plays a crucial role in plant breeding and genetic improvement. Although the phenomenon of polyploidization affecting the area and number of plant epidermal pavement cells is well described, the underlying mechanism behind this phenomenon is still largely unknown. In this study, we found that the leaves of autotetraploid birch (Betula pendula) stopped cell division earlier and had a larger cell area. In addition, compared to diploids, tetraploids have a smaller stomatal density and fewer stomatal numbers. Genome-wide DNA methylation analysis revealed no significant difference in global DNA methylation levels between diploids and tetraploids. A total of 9154 differential methylation regions (DMRs) were identified between diploids and tetraploids, with CHH-type DMRs accounting for 91.73% of all types of DMRs. Further research has found that there are a total of 2105 differentially methylated genes (DMEGs) with CHH-type DMRs in birch. The GO functional enrichment results of DMEGs showed that differentially methylated genes were mainly involved in terms such as cellular process and metabolic process. The analysis of differentially methylated genes and differentially expressed genes suggests that hyper-methylation in the promoter region may inhibit the gene expression level of BpCYCD3;2 in tetraploids. To investigate the function of BpCYCD3;2 in birch, we obtained overexpression and repressed expression lines of BpCYCD3;2 through genetic transformation. The morphogenesis of both BpCYCD3;2-OE and BpCYCD3;2-RE lines was not affected. However, low expression of BpCYCD3;2 can lead to inhibition of cell division in leaves, and this inhibition of cell proliferation can be compensated for by an increase in cell size. Additionally, we found that the number and density of stomata in the BpCYCD3;2-RE lines were significantly reduced, consistent with the tetraploid. These data indicate that changes in cell division ability and stomatal changes in tetraploid birch can be partially attributed to low expression of the BpCYCD3;2 gene, which may be related to hyper-methylation in its promoter region. These results will provide new insights into the mechanism by which polyploidization affects plant development.

摘要

多倍体化在植物育种和遗传改良中起着至关重要的作用。尽管多倍体化影响植物表皮铺面砖细胞的面积和数量的现象已得到很好的描述,但这一现象背后的机制在很大程度上仍不清楚。在这项研究中,我们发现自交四倍体桦树(Betula pendula)的叶片更早停止细胞分裂,且细胞面积更大。此外,与二倍体相比,四倍体的气孔密度更小,气孔数量更少。全基因组 DNA 甲基化分析显示,二倍体和四倍体之间的全基因组 DNA 甲基化水平没有显著差异。在二倍体和四倍体之间共鉴定到 9154 个差异甲基化区域(DMR),其中 CHH 型 DMR 占所有 DMR 类型的 91.73%。进一步的研究发现,桦树中共有 2105 个具有 CHH 型 DMR 的差异甲基化基因(DMEG)。DMEG 的 GO 功能富集结果表明,差异甲基化基因主要涉及细胞过程和代谢过程等术语。差异甲基化基因和差异表达基因的分析表明,启动子区域的高甲基化可能抑制了四倍体中 BpCYCD3;2 的基因表达水平。为了研究 BpCYCD3;2 在桦树中的功能,我们通过遗传转化获得了 BpCYCD3;2 的过表达和抑制表达系。BpCYCD3;2-OE 和 BpCYCD3;2-RE 系的形态发生均不受影响。然而,BpCYCD3;2 的低表达会导致叶片细胞分裂受到抑制,而这种细胞增殖的抑制可以通过细胞大小的增加来补偿。此外,我们发现 BpCYCD3;2-RE 系的气孔数量和密度显著降低,与四倍体一致。这些数据表明,四倍体桦树中细胞分裂能力的变化和气孔的变化可以部分归因于 BpCYCD3;2 基因的低表达,这可能与其启动子区域的高甲基化有关。这些结果将为多倍体化如何影响植物发育的机制提供新的见解。

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