Live imaging of Arabidopsis shoot primordia via a confocal laser scanning microscope

Summary: Live imaging through confocal laser scanning microscopy enables the recording, analysis, and comparison of the dynamics of shapes and gene expression patterns of plant shoot apical meristems (SAMs) or primordia. Here, we provide a protocol to describe the preparation process of imaging Arab...

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Main Authors: Ziyuan Peng, Yuling Jiao, Ying Wang
Format: Article
Language:English
Published: Elsevier 2023-06-01
Series:STAR Protocols
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2666166723001752
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author Ziyuan Peng
Yuling Jiao
Ying Wang
author_facet Ziyuan Peng
Yuling Jiao
Ying Wang
author_sort Ziyuan Peng
collection DOAJ
description Summary: Live imaging through confocal laser scanning microscopy enables the recording, analysis, and comparison of the dynamics of shapes and gene expression patterns of plant shoot apical meristems (SAMs) or primordia. Here, we provide a protocol to describe the preparation process of imaging Arabidopsis SAMs and primordia using a confocal microscope. We describe steps for dissection, visualization of meristems using dyes and fluorescent proteins, and gain 3D morphology of meristems. We then detail analysis of shoot meristems using time-lapse imaging.For complete details on the use and execution of this protocol, please refer to Peng et al. (2022).1 : Publisher’s note: Undertaking any experimental protocol requires adherence to local institutional guidelines for laboratory safety and ethics.
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spelling doaj.art-01b4ed004a0543fa94dfeb6442e0ff4d2023-04-07T06:50:58ZengElsevierSTAR Protocols2666-16672023-06-0142102217Live imaging of Arabidopsis shoot primordia via a confocal laser scanning microscopeZiyuan Peng0Yuling Jiao1Ying Wang2College of Life Sciences, University of Chinese Academy of Sciences, Beijing 100049, ChinaState Key Laboratory of Protein and Plant Gene Research, School of Life Sciences, Peking University, Beijing 100871, China; Peking-Tsinghua Center for Life Sciences, Center for Quantitative Biology, Academy for Advanced Interdisciplinary Studies, Peking University, Beijing 100871, China; Corresponding authorCollege of Life Sciences, University of Chinese Academy of Sciences, Beijing 100049, China; Corresponding authorSummary: Live imaging through confocal laser scanning microscopy enables the recording, analysis, and comparison of the dynamics of shapes and gene expression patterns of plant shoot apical meristems (SAMs) or primordia. Here, we provide a protocol to describe the preparation process of imaging Arabidopsis SAMs and primordia using a confocal microscope. We describe steps for dissection, visualization of meristems using dyes and fluorescent proteins, and gain 3D morphology of meristems. We then detail analysis of shoot meristems using time-lapse imaging.For complete details on the use and execution of this protocol, please refer to Peng et al. (2022).1 : Publisher’s note: Undertaking any experimental protocol requires adherence to local institutional guidelines for laboratory safety and ethics.http://www.sciencedirect.com/science/article/pii/S2666166723001752Developmental biologyMicroscopyModel OrganismsPlant sciences
spellingShingle Ziyuan Peng
Yuling Jiao
Ying Wang
Live imaging of Arabidopsis shoot primordia via a confocal laser scanning microscope
STAR Protocols
Developmental biology
Microscopy
Model Organisms
Plant sciences
title Live imaging of Arabidopsis shoot primordia via a confocal laser scanning microscope
title_full Live imaging of Arabidopsis shoot primordia via a confocal laser scanning microscope
title_fullStr Live imaging of Arabidopsis shoot primordia via a confocal laser scanning microscope
title_full_unstemmed Live imaging of Arabidopsis shoot primordia via a confocal laser scanning microscope
title_short Live imaging of Arabidopsis shoot primordia via a confocal laser scanning microscope
title_sort live imaging of arabidopsis shoot primordia via a confocal laser scanning microscope
topic Developmental biology
Microscopy
Model Organisms
Plant sciences
url http://www.sciencedirect.com/science/article/pii/S2666166723001752
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AT yulingjiao liveimagingofarabidopsisshootprimordiaviaaconfocallaserscanningmicroscope
AT yingwang liveimagingofarabidopsisshootprimordiaviaaconfocallaserscanningmicroscope