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衰老相关基因 101(PagSAG101a)在杨树次生木质部形成中的调节作用。

The role of senescence-associated gene101 (PagSAG101a) in the regulation of secondary xylem formation in poplar.

机构信息

State Key Laboratory of Tree Genetics and Breeding, Research Institute of Forestry, Chinese Academy of Forestry, Beijing, 100091, China.

State Key Laboratory of Subtropical Silviculture, College of Forestry and Biotechnology, Zhejiang A & F University, Hangzhou, 311300, China.

出版信息

J Integr Plant Biol. 2022 Jan;64(1):73-86. doi: 10.1111/jipb.13195.

Abstract

Wood is produced by the accumulation of secondary xylem via proliferation and differentiation of the cambium cells in woody plants. Identifying the regulators involved in this process remains a challenging task. In this study, we isolated PagSAG101a, the homolog of Arabidopsis thaliana SAG101, from a hybrid poplar (Populus alba × Populus glandulosa) clone 84K and investigated its role in secondary xylem development. PagSAG101a was expressed predominantly in lignified stems and localized in the nucleus. Compared with non-transgenic 84K plants, transgenic plants overexpressing PagSAG101a displayed increased plant height, internode number, stem diameter, xylem width, and secondary cell wall thickness, while opposite phenotypes were observed for PagSAG101a knock-out plants. Transcriptome analyses revealed that differentially expressed genes were enriched for those controlling cambium cell division activity and subsequent secondary cell wall deposition during xylem formation. In addition, the tandem CCCH zinc finger protein PagC3H17, which positively regulates secondary xylem width and secondary wall thickening in poplar, could bind to the promoter of PagSAG101a and mediate the regulation of xylem differentiation. Our results support that PagSAG101a, downstream of PagC3H17, functions in wood development.

摘要

木材是通过木本植物形成层细胞的增殖和分化积累次生木质部而产生的。鉴定参与这一过程的调节因子仍然是一项具有挑战性的任务。在这项研究中,我们从杂交杨(白杨×腺柳)84K 克隆中分离出拟南芥 SAG101 的同源物 PagSAG101a,并研究了其在次生木质部发育中的作用。PagSAG101a 在木质化茎中表达强烈,定位于细胞核中。与非转基因 84K 植物相比,过表达 PagSAG101a 的转基因植物表现出较高的株高、节间数、茎直径、木质部宽度和次生细胞壁厚度,而 PagSAG101a 敲除植物则表现出相反的表型。转录组分析表明,差异表达基因富集于控制形成层细胞分裂活性和随后木质部形成过程中次生细胞壁沉积的基因。此外,串联 CCCH 锌指蛋白 PagC3H17 正向调控杨树次生木质部宽度和次生壁增厚,可与 PagSAG101a 的启动子结合,并介导木质部分化的调节。我们的结果支持 PagSAG101a 在 PagC3H17 下游参与木材发育。

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