| Literature DB >> 31975296 |
Merijn Kerstens1, Soeren Strauss2, Richard Smith2, Viola Willemsen3.
Abstract
Development and growth of plant organs is determined by a myriad of molecular processes that occur in each individual cell. As a direct consequence of these processes, cells alter in size and shape. They therefore serve as excellent parameters to thoroughly understand gene function. However, conventional single-plane analyses fail to accurately capture cell metrics. Here, we present a comprehensive illustrated guide that demonstrates how SCRI Renaissance 2200 staining of Arabidopsis thaliana embryos and roots can be combined with the open-source application MorphoGraphX to quantify cell parameters in 3D. We compare this staining method with other common staining techniques and provide examples of embryo and root tissue segmentation. With our novel approach, subtle single-cell phenotypes can be identified in their native context, providing new possibilities to dissect gene networks.Entities:
Keywords: 3D imaging; 3D segmentation; Cell volume; Embryos; Lateral roots; MorphoGraphX; Roots; SCRI Renaissance
Year: 2020 PMID: 31975296 DOI: 10.1007/978-1-0716-0342-0_6
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745