抄録
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.
本文言語 | English |
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ページ(範囲) | 904-908 |
ページ数 | 5 |
ジャーナル | Plant and Cell Physiology |
巻 | 50 |
号 | 4 |
DOI | |
出版ステータス | Published - 4月 2009 |
ASJC Scopus subject areas
- 生理学
- 植物科学
- 細胞生物学