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First published online April 6, 2007; 10.1105/tpc.106.042911

The Plant Cell 19:1362-1375 (2007)
© 2007 American Society of Plant Biologists

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Rice NON-YELLOW COLORING1 Is Involved in Light-Harvesting Complex II and Grana Degradation during Leaf Senescence[W]

Makoto Kusabaa,1, Hisashi Itob, Ryouhei Moritac, Shuichi Iidad, Yutaka Satoa, Masaru Fujimotoa, Shinji Kawasakie, Ryouichi Tanakab, Hirohiko Hirochikae, Minoru Nishimurac and Ayumi Tanakab

a Graduate School of Agricultural and Life Sciences, University of Tokyo, Tokyo 113-8657, Japan
b Institute of Low-Temperature Science, Hokkaido University, Sapporo 060-0819, Japan
c Institute of Radiation Breeding, National Institute of Agrobiological Sciences, Hitachiohmiya 219-2293, Japan
d Chugoku National Agricultural Research Center for Western Region, National Agriculture and Bio-oriented Research Organization, Fukuyama 721-0975, Japan
e National Institute of Agrobiological Sciences, Tsukuba 305-8602, Japan

1 To whom correspondence should be addressed. E-mail akusaba{at}mail.ecc.u-tokyo.ac.jp; fax 81-3-5841-5063.

Chlorophyll degradation is an aspect of leaf senescence, which is an active process to salvage nutrients from old tissues. non-yellow coloring1 (nyc1) is a rice (Oryza sativa) stay-green mutant in which chlorophyll degradation during senescence is impaired. Pigment analysis revealed that degradation of not only chlorophylls but also light-harvesting complex II (LHCII)–bound carotenoids was repressed in nyc1, in which most LHCII isoforms were selectively retained during senescence. Ultrastructural analysis of nyc1 chloroplasts revealed that large and thick grana were present even in the late stage of senescence, suggesting that degradation of LHCII is required for the proper degeneration of thylakoid membranes. Map-based cloning of NYC1 revealed that it encodes a chloroplast-localized short-chain dehydrogenase/reductase (SDR) with three transmembrane domains. The predicted structure of the NYC1 protein and the phenotype of the nyc1 mutant suggest the possibility that NYC1 is a chlorophyll b reductase. Although we were unable to detect the chlorophyll b reductase activity of NYC1, NOL (for NYC1-like), a protein closely related to NYC1 in rice, showed chlorophyll b reductase activity in vitro. We suggest that NYC1 and NOL encode chlorophyll b reductases with divergent functions. Our data collectively suggest that the identified SDR protein NYC1 plays essential roles in the regulation of LHCII and thylakoid membrane degradation during senescence.


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