Volume 17, Issue 17 p. 1616-1620
Communication

Eudistomin C, an Antitumor and Antiviral Natural Product, Targets 40S Ribosome and Inhibits Protein Translation

Yu Ota

Faculty of Life and Environmental Sciences, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki, 305-8572 Japan

These authors contributed equally to this work.

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Dr. Takumi Chinen

Faculty of Life and Environmental Sciences, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki, 305-8572 Japan

These authors contributed equally to this work.

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Keisuke Yoshida

Faculty of Life and Environmental Sciences, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki, 305-8572 Japan

These authors contributed equally to this work.

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Shun Kudo

Faculty of Life and Environmental Sciences, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki, 305-8572 Japan

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Prof. Dr. Yoko Nagumo

Faculty of Life and Environmental Sciences, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki, 305-8572 Japan

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Dr. Yuh Shiwa

NODAI Genome Research Center, Tokyo University of Agriculture, 1-1-1 Sakuragaoka, Setagaya-ku, Tokyo, 156-8502 Japan

Division of Biobank and Data Management, Iwate Tohoku Medical Megabank Organization, Iwate Medical University, Yahaba-cho, Shiwa-gun, Iwate, 028-3694 Japan

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Ryosuke Yamada

Graduate School of Pharmaceutical Sciences, Nagoya University, Furo-cho, Chikusa-ku, Nagoya, 464-8601 Japan

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Dr. Hirotatsu Umihara

Graduate School of Pharmaceutical Sciences, Nagoya University, Furo-cho, Chikusa-ku, Nagoya, 464-8601 Japan

Graduate School of Pharmaceutical Sciences, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-0033 Japan

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Dr. Kotaro Iwasaki

Graduate School of Pharmaceutical Sciences, University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-0033 Japan

Graduate School of Life Sciences, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai, 980-8577 Japan

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Dr. Hiroshi Masumoto

Biomedical Research Support Center, Nagasaki University School of Medicine, 1-12-4 Sakamoto, Nagasaki, Nagasaki, 852-8523 Japan

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Prof. Dr. Satoshi Yokoshima

Graduate School of Pharmaceutical Sciences, Nagoya University, Furo-cho, Chikusa-ku, Nagoya, 464-8601 Japan

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Prof. Dr. Hirofumi Yoshikawa

NODAI Genome Research Center, Tokyo University of Agriculture, 1-1-1 Sakuragaoka, Setagaya-ku, Tokyo, 156-8502 Japan

Department of Bioscience, Tokyo University of Agriculture, 1-1-1 Sakuragaoka, Setagaya-ku, Tokyo, 156-8502 Japan

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Prof. Dr. Tohru Fukuyama

Graduate School of Pharmaceutical Sciences, Nagoya University, Furo-cho, Chikusa-ku, Nagoya, 464-8601 Japan

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Prof. Dr. Junichi Kobayashi

Graduate School of Pharmaceutical Sciences, Hokkaido University, Sapporo, 060-0812 Japan

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Prof. Dr. Takeo Usui

Corresponding Author

Faculty of Life and Environmental Sciences, University of Tsukuba, 1-1-1 Tennodai, Tsukuba, Ibaraki, 305-8572 Japan

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First published: 15 June 2016
Citations: 8

Abstract

Powerful undercurrents: Eudistomin C, a marine natural product, shows potent antitumor and antiviral activities, but the target molecule and the mechanism of action remain to be elucidated. Here, we show that this compound binds to uS11‐containing 40S ribosomal subunit, and achieves cytotoxicity by inhibiting protein translation.

Abstract

Eudistomin C (EudiC), a natural product, shows potent antitumor and antiviral activities, but the target molecule and the mechanism of action remain to be revealed. Here, we show that the 40S ribosome is the target in EudiC cytotoxicity. We isolated EudiC‐resistant mutants from a multidrug‐sensitive yeast strain, and a genetic analysis classified these YER (yeast EudiC resistance) mutants into three complementation groups. A genome‐wide study revealed that the YER1‐6 mutation is in the uS11 gene (RPS14A). Biotinylated EudiC pulled down Rps14p‐containing complexes from 40S and 80S ribosomes, but not from the 60S ribosome. EudiC strongly inhibited translation of the wild‐type strain but not of YER1‐6 in cells and in vitro. These results indicate that EudiC is a protein synthesis inhibitor targeting the uS11‐containing ribosomal subunit, and shows cytotoxicity by inhibiting protein translation.