CZON-cutter – a CRISPR-Cas9 system for multiplexed organelle imaging in a simple unicellular alga

Author:

Tanaka Naoto1,Mogi Yuko1,Fujiwara Takayuki23,Yabe Kannosuke1,Toyama Yukiho1,Higashiyama Tetsuya145,Yoshida Yamato16ORCID

Affiliation:

1. Department of Biological Sciences, Graduate School of Science, The University of Tokyo, 7-3-1 Hongo, Bunkyo, Tokyo 113-0033, Japan

2. Department of Gene Function and Phenomics, National Institute of Genetics, Mishima, Shizuoka 411-8540, Japan

3. Department of Genetics, Graduate University for Advanced Studies, SOKENDAI, Mishima, Shizuoka 411-8540, Japan

4. Division of Biological Science, Graduate School of Science, Nagoya University, Furo-cho, Chikusa-ku, Nagoya, Aichi 464-8602, Japan

5. Institute of Transformative Bio-Molecules (WPI-ITbM), Nagoya University, Furo-cho, Chikusa-ku, Nagoya, Aichi 464-8601, Japan

6. Japan Science and Technology Agency (JST), PRESTO, 7-3-1 Hongo, Bunkyo, Tokyo 113-0033, Japan

Abstract

ABSTRACT The unicellular alga Cyanidioschyzon merolae has a simple cellular structure; each cell has one nucleus, one mitochondrion, one chloroplast and one peroxisome. This simplicity offers unique advantages for investigating organellar proliferation and the cell cycle. Here, we describe CZON-cutter, an engineered clustered, regularly interspaced, short palindromic repeats (CRISPR)/CRISPR-associated nuclease 9 (Cas9) system for simultaneous genome editing and organellar visualization. We engineered a C. merolae strain expressing a nuclear-localized Cas9–Venus nuclease for targeted editing of any locus defined by a single-guide RNA (sgRNA). We then successfully edited the algal genome and visualized the mitochondrion and peroxisome in transformants using fluorescent protein reporters with different excitation wavelengths. Fluorescent protein labeling of organelles in living transformants allows us to validate phenotypes associated with organellar proliferation and the cell cycle, even when the edited gene is essential. Combined with the exceptional biological features of C. merolae, CZON-cutter will be instrumental for investigating cellular and organellar division in a high-throughput manner. This article has an associated First Person interview with the first author of the paper.

Funder

Japan Science and Technology Agency

Human Frontier Science Program

Japan Society for the Promotion of Science

Sumitomo Foundation

Institute for Fermentation, Osaka

Publisher

The Company of Biologists

Subject

Cell Biology

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