Abstract
Visualizing organelles in living cells is a powerful method to analyze their intrinsic mechanisms. Easy observation of chlorophyll facilitates the study of the underlying mechanisms in chloroplasts, but not in other plastid types. Here, we constructed a transgenic plant enabling visualization of plastids in pollen grains. Combination of a plastid-targeted fluorescent protein with a pollen-specific promoter allowed us to observe the precise number, size and morphology of plastids in pollen grains of the wild type and the ftsZ1 mutant, whose responsible gene plays a central role in chloroplast division. The transgenic material presented in this work is useful for studying the division mechanism of pollen plastids.
Original language | English |
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Pages (from-to) | 904-908 |
Number of pages | 5 |
Journal | Plant and Cell Physiology |
Volume | 50 |
Issue number | 4 |
DOIs | |
Publication status | Published - Apr 2009 |
Keywords
- Fluorescent protein
- FtsZ1
- Male gametophyte
- Plastid division
- Pollen
ASJC Scopus subject areas
- Physiology
- Plant Science
- Cell Biology