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转录组分析揭示了芹菜叶柄组织中层细胞细胞壁形成的特点。

Transcriptome profiling of celery petiole tissues reveals peculiarities of the collenchyma cell wall formation.

机构信息

Laboratory of Plant Glycobiology, Kazan Institute of Biochemistry and Biophysics, FRC Kazan Scientific Center of RAS, Lobachevsky Str., 2/31, 420111, Kazan, Russia.

Unité de Glycobiologie Structurale et Fonctionnelle, UMR 8576, CNRS, Université de Lille, 59655, Villeneuve d'Ascq, France.

出版信息

Planta. 2022 Dec 20;257(1):18. doi: 10.1007/s00425-022-04042-7.

Abstract

Transcriptome and biochemical analyses are applied to individual plant cell types to reveal potential players involved in the molecular machinery of cell wall formation in specialized cells such as collenchyma. Plant collenchyma is a mechanical tissue characterized by an irregular, thickened cell wall and the ability to support cell elongation. The composition of the collenchyma cell wall resembles that of the primary cell wall and includes cellulose, xyloglucan, and pectin; lignin is absent. Thus, the processes associated with the formation of the primary cell wall in the collenchyma can be more pronounced compared to other tissues due to its thickening. Primary cell walls intrinsic to different tissues may differ in structure and composition, which should be reflected at the transcriptomic level. For the first time, we conducted transcriptome profiling of collenchyma strands isolated from young celery petioles and compared them with other tissues, such as parenchyma and vascular bundles. Genes encoding proteins involved in the primary cell wall formation during cell elongation, such as xyloglucan endotransglucosylase/hydrolases, expansins, and leucine-rich repeat proteins, were significantly activated in the collenchyma. As the key players in the transcriptome orchestra of collenchyma, xyloglucan endotransglucosylase/hydrolase transcripts were characterized in more detail, including phylogeny and expression patterns. The comprehensive approach that included transcriptome and biochemical analyses allowed us to reveal peculiarities of collenchyma cell wall formation and modification, matching the abundance of upregulated transcripts and their potential substrates for revealed gene products. As a result, specific isoforms of multigene families were determined for further functional investigation.

摘要

对单个植物细胞类型进行转录组和生化分析,以揭示参与厚角组织等特化细胞细胞壁形成分子机制的潜在因子。植物厚角组织是一种机械组织,其特征为不规则加厚的细胞壁和支持细胞伸长的能力。厚角组织细胞壁的组成类似于初生细胞壁,包括纤维素、木葡聚糖和果胶;没有木质素。因此,与其他组织相比,由于其加厚,与厚角组织初生细胞壁形成相关的过程可能更为明显。不同组织中固有的初生细胞壁在结构和组成上可能存在差异,这应该在转录组水平上反映出来。我们首次对从小芹叶柄中分离出的厚角组织进行了转录组分析,并将其与其他组织(如薄壁组织和维管束)进行了比较。在厚角组织中,参与细胞伸长过程中初生细胞壁形成的基因,如木葡聚糖内转糖苷酶/水解酶、扩展蛋白和富含亮氨酸重复蛋白的基因,明显被激活。木葡聚糖内转糖苷酶/水解酶转录本作为厚角组织转录组乐队的关键因子,其系统发育和表达模式得到了更详细的描述。包括转录组和生化分析在内的综合方法使我们能够揭示厚角组织细胞壁形成和修饰的特点,与上调转录本的丰度及其潜在的产物基因的底物相匹配。结果,确定了多基因家族的特定同工型,以进行进一步的功能研究。

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