Department of Plant Biology, Cornell University, Ithaca, NY 14853, USA.
J Exp Bot. 2010 Jul;61(12):3321-30. doi: 10.1093/jxb/erq153. Epub 2010 Jun 2.
Most studies of the biochemical and regulatory pathways that are associated with, and control, fruit expansion and ripening are based on homogenized bulk tissues, and do not take into consideration the multiplicity of different cell types from which the analytes, be they transcripts, proteins or metabolites, are extracted. Consequently, potentially valuable spatial information is lost and the lower abundance cellular components that are expressed only in certain cell types can be diluted below the level of detection. In this study, laser microdissection (LMD) was used to isolate epidermal and subepidermal cells from green, expanding Citrus clementina fruit and their transcriptomes were compared using a 20k citrus cDNA microarray and quantitative real-time PCR. The results show striking differences in gene expression profiles between the two cell types, revealing specific metabolic pathways that can be related to their respective organelle composition and cell wall specialization. Microscopy provided additional evidence of tissue specialization that could be associated with the transcript profiles with distinct differences in organelle and metabolite accumulation. Subepidermis predominant genes are primarily involved in photosynthesis- and energy-related processes, as well as cell wall biosynthesis and restructuring. By contrast, the most epidermis predominant genes are related to the biosynthesis of the cuticle, flavonoids, and defence responses. Furthermore, the epidermis transcript profile showed a high proportion of genes with no known function, supporting the original hypothesis that analysis at the tissue/cell specific levels can promote gene discovery and lead to a better understanding of the specialized contribution of each tissue to fruit physiology.
大多数研究与果实扩张和成熟相关的生化和调控途径,以及控制这些途径的生化和调控途径,都是基于均质的组织进行的,并没有考虑到分析物(无论是转录本、蛋白质还是代谢物)提取自的多种不同细胞类型。因此,潜在有价值的空间信息丢失了,而且仅在某些细胞类型中表达的丰度较低的细胞成分可能会被稀释到检测水平以下。在这项研究中,激光微切割(LMD)用于从绿色、扩张的克莱门氏小柑橘果实中分离表皮和表皮下细胞,并使用 20k 柑橘 cDNA 微阵列和定量实时 PCR 比较它们的转录组。结果表明,两种细胞类型的基因表达谱存在显著差异,揭示了特定的代谢途径,这些途径可以与它们各自的细胞器组成和细胞壁特化相关联。显微镜提供了组织特化的额外证据,这些证据可能与转录谱相关联,而在细胞器和代谢物积累方面存在明显差异。表皮下细胞优势基因主要参与光合作用和能量相关过程,以及细胞壁生物合成和重构。相比之下,最表皮优势基因与角质层、类黄酮和防御反应的生物合成有关。此外,表皮转录谱显示出具有未知功能的基因比例很高,这支持了最初的假设,即组织/细胞特异性分析可以促进基因发现,并更好地理解每个组织对果实生理学的专门贡献。