Detail of Fig2c_NIR_SYBR_Arabi_Pollen_nucleus_WT


Project
SSBD:Repository
Title
The time-lapse NIR autofluorescence and SYBR Green I images of vegetative nucleus during pollen tube elongation in wild-type Arabidopsis
Description
The DNA of wild-type Arabidopsis Col-0 was co-stained with SYBR Green I, a green fluorescent dye, to measure nuclear near-infrared (NIR) autofluorescence in pollen. Time-lapse NIR autofluorescence imaging revealed the dynamics of the vegetative nucleus during pollen tube elongation in wild-type Arabidopsis. The NIR autofluorescence promoted clearer imaging of the vegetative nucleus than DNA dyes during pollen tube elongation.
Release, Updated
2026-06-09
License
CC BY 4.0
Kind
Image data
File Formats
czi
Data size
106.9 MB

Organism
Arabidopsis thaliana ( NCBI:txid3702 )
Strain(s)
-
Cell Line
-

Datatype
-
Molecular Function (MF)
Biological Process (BP)
pollen tube development
Cellular Component (CC)
pollen tube
Biological Imaging Method
confocal microscopy (FBbi_00000251) fluorescence microscopy (FBbi_00000246) time lapse microscopy (FBbi_00000249)
X scale
0.198 micrometer
Y scale
0.198 micrometer
Z scale
-
T scale
14.90 sec

Image Acquisition
Experiment type
-
Microscope type
-
Acquisition mode
-
Contrast method
-
Microscope model
-
Detector model
-
Objective model
-
Filter set
-

Summary of Methods
Yoshinari A, Isoda R, Yagi N, Sato Y, Lindeboom JJ, Ehrhardt DW, Frommer WB, Nakamura M. Near-infrared imaging of phytochrome-derived autofluorescence in plant nuclei. Plant J. 2024 Jun;118(5):1699-1712.
Related paper(s)

Akira Yoshinari, Reika Isoda, Noriyoshi Yagi, Yoshikatsu Sato, Jelmer J Lindeboom, David W Ehrhardt, Wolf B Frommer, Masayoshi Nakamura (2024) Near-infrared imaging of phytochrome-derived autofluorescence in plant nuclei., The Plant journal : for cell and molecular biology

Published in 2024 Mar 20 (Electronic publication in March 20, 2024, midnight )

(Abstract) Capturing images of the nuclear dynamics within live cells is an essential technique for comprehending the intricate biological processes inherent to plant cell nuclei. While various methods exist for imaging nuclei, including combining fluorescent proteins and dyes with microscopy, there is a dearth of commercially available dyes for live-cell imaging. In Arabidopsis thaliana, we discovered that nuclei emit autofluorescence in the near-infrared (NIR) range of the spectrum and devised a non-invasive technique for the visualization of live cell nuclei using this inherent NIR autofluorescence. Our studies demonstrated the capability of the NIR imaging technique to visualize the dynamic behavior of nuclei within primary roots, root hairs, and pollen tubes, which are tissues that harbor a limited number of other organelles displaying autofluorescence. We further demonstrated the applicability of NIR autofluorescence imaging in various other tissues by incorporating fluorescence lifetime imaging techniques. Nuclear autofluorescence was also detected across a wide range of plant species, enabling analyses without the need for transformation. The nuclear autofluorescence in the NIR wavelength range was not observed in animal or yeast cells. Genetic analysis revealed that this autofluorescence was caused by the phytochrome protein. Our studies demonstrated that nuclear autofluorescence imaging can be effectively employed not only in model plants but also for studying nuclei in non-model plant species.

Contact
Akira Yoshinari, Masayoshi Nakamura , Nagoya University, Nagoya University , Institute of Transformative Bio-Molecules, Institute of Transformative Bio-Molecules , Institute of Transformative Bio-Molecules, Institute of Transformative Bio-Molecules
Contributors

OMERO Dataset
OMERO Project
Source