Plant Molecular Genetics

Staff

Toshiharu Shikanai

Position
Professor
Office
Science Building 2, Room 210
Phone
075-753-4247
Fax
075-753-4257
Email
shikanai(at-mark)pmg.bot.kyoto-u.ac.jp

Mizuki Takenaka

Position
Associate Professor
Office
Science Building 2, Room 210
Phone
075-753-4246
Fax
075-753-4257
Email
mizuki.takenaka(at-mark)pmg.bot.kyoto-u.ac.jp

Ryuji Tsugeki

Position
Assistant Professor
Office
Science Building 2, Room 222
Phone
075-753-4147
Fax
075-753-4257
Email
tsugeki.ryuji.5a(at-mark)kyoto-u.ac.jp

Research

1. Studies on the regulation of photosynthetic electron transfer

(1) Research on chloroplast proton driving force control

Photosynthesis converts the light energy of the sun into chemical energy that can be used by life, but the reception of excess light energy destroys the photosynthesis device through the production of reactive oxygen species. Plants regulate photosynthetic electron transfer to avoid this photodamage and maintain maximum photosynthetic activity. We are aiming to elucidate this molecular mechanism.

Fig. 1. Visualization of photosynthetic electron transfer control.

2. RNA editing mechanism of plant mitochondria and chloroplasts

RNA editing of terrestrial plant mitochondria and chloroplasts converts specific cytidine (C) on the RNA sequence to uridine (U) and is essential for the functional expression of normal organelle proteins. So far, we have identified a number of RNA editing factors, such as the PPR protein required for specific selection of C to be edited and the MORF protein involved in dozens of RNA editing sites. Currently, we are aiming to identify new RNA editing factors, including proteins with enzymatic activity, which is one of the biggest mysteries of RNA editing, and are proceeding with analysis of how each factor is involved in RNA editing. We also aim to reconstruct an active RNA editing complex by combining these factors.

Fig. 2. Model of RNA editing complex. Multiple PPR and MORF proteins are involved.

3. Research on plant stem cells

A characteristic of plant development is that organogenesis is repeated after embryogenesis. We are proceeding with the identification and analysis of genes important for plant organogenesis and stem cell maintenance.

Fig. 3. The blue part in the figure is a collection of stem cells, and organs such as leaves are made from here.

4. Research on “chromosomes” of chloroplasts and mitochondria

Chloroplasts and mitochondria have their own DNA. These chloroplast / mitochondrial DNA combine with various proteins to form a “nucleoid”. The nucleoid, like the chromosome in the cell nucleus, is the functional center of chloroplast / mitochondrial DNA replication, repair, gene expression, and inheritance, and is the center of vital activities such as photosynthesis and respiration. We want to explore the structure, function and evolution of these chloroplasts / mitochondrial nucleoids.

Fig. 4. Uneven distribution of chloroplast nucleoids (yellow bright spots: arrows) in mutants lacking Holliday junction dissociation enzyme (upper figure). Holliday junction (left in the figure below) and cleavage by dissociation enzyme (center arrow in the figure below) visualized by DNA origami and high-speed atomic force microscopy (right in the figure below).