Single-nuclei sequencing of Moricandia arvensis reveals bundle sheath cell function in the photorespiratory shuttle of C3-C4 intermediate Brassicaceae.
Sebastian Triesch, Vanessa Reichel-Deland, José Miguel Valderrama Martín, Michael Melzer, Urte Schlüter, Andreas P M Weber
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引用次数: 0
Abstract
Spatially confined gene expression determines cell identity and is fundamental to complex plant traits. In the evolutionary transition from C3 to the more efficient C4 photosynthesis, restricting the glycine decarboxylase reaction to bundle sheath cells initiates a carbon concentrating mechanism via the photorespiratory glycine shuttle. This evolutionary step is generally thought to play an essential role in the progression from ancestral C3 to C4 photosynthesis. Plants operating this shuttle are often referred to as C3-C4 intermediates or C2 species. Within the Brassicaceae family, which includes model plants and crops, such species have evolved independently at least five times. However, research on the biochemistry of C3-C4 intermediates in the Brassicaceae has been limited to a few case studies of differentially localized proteins between mesophyll and bundle sheath cells. Here, we leveraged recent advances in single-cell transcriptome sequencing to better understand how cellular specialization affects interconnected pathways. We generated a single-nuclei RNA sequencing dataset for Moricandia arvensis, a Brassicaceae with C3-C4 intermediate characteristics, and compared it to a publicly available single-cell transcriptome of leaf tissue of the C3 Arabidopsis thaliana. We independently confirmed the localization of selected photorespiratory proteins by electron microscopy of immunogold-labelled leaf sections. Our analysis revealed a M. arvensis specific shift in expression of genes directly associated with the photorespiratory reactions, including components of the glycine decarboxylase complex, the glutamate:glyoxylate aminotransferase (GGT) and the glycolate oxidase (GOX) suggesting a shuttle of several C2 metabolites to the bundles sheath. Additionally associated pathways such as ammonium assimilation, synthesis of specific amino acids, redox regulation, and transport also showed enhanced abundance in the M. arvensis bundle sheath.
期刊介绍:
The Journal of Experimental Botany publishes high-quality primary research and review papers in the plant sciences. These papers cover a range of disciplines from molecular and cellular physiology and biochemistry through whole plant physiology to community physiology.
Full-length primary papers should contribute to our understanding of how plants develop and function, and should provide new insights into biological processes. The journal will not publish purely descriptive papers or papers that report a well-known process in a species in which the process has not been identified previously. Articles should be concise and generally limited to 10 printed pages.