Cytoplasmic male sterility in rice

Cytoplasmic male sterility (CMS) is used for hybrid seed production including rice. In CMS, a male sterility gene in mitochondria causes failure of development of a male reproductive organ or pollen, and male sterility is restored by a nuclear gene that encodes a protein localized in mitochondria and suppresses a corresponding male sterility gene. We have been studying to understand mechanisms of CMS by identifying a male sterility gene, a restorer of fertility gene and their interaction. We also have been trying to develop novel CMS lines of rice.

CMS of rice is often observed in a sibling obtained by successive back crossing between distantly related cultivars or strains, and various different types of CMS exist in rice. This means that a different restorer of fertility (Rf) gene suppresses its corresponding CMS gene with a different mechanism. For example, in BT-type CMS, Rf1, which encodes mitochondria-localized pentatricopeptide repeat (PPR) protein, suppresses mitochondrial CMS gene orf79 by an RNA-processing mechanism. CW-type CMS shows a very unique mechanism. Rf17 gene is expressed at a normal level in a nucleus of a fertile plant. However, in combination with a corresponding CMS gene in mitochondria, the expression level of Rf17 is up-regulated, which results in male sterility. An Rf17 allele whose expression is not up-regulated even in the presence of the CMS gene plays a role for an Rf gene.

We have been generating various types of CMS plants in rice , and analysing their Rf genes, CMS genes and their interaction using molecular genetics and genetic engineering techniques.

A flower of wild rice and pollens of CMS lines of cultivated rice. Mitochondria determine pollen fates. T65: Taichung 65 (fertile), WA, BT, CW: CMS lines.

Takatsuka et al (2021) Rice 14, 46

Omukai et al (2021) Plant Physiol 187, 236-246

Toriyama (2021) Plant Biotechnol 38, 285-295

Suketomo et al (2020) Plant Biotechnol 37, 285-292

Toriyama et al (2019) Rice 12, 73

Kazama et al (2019) Nat Plants 5, 722-730

Igarashi et al (2016) Plant Cell Physiol 57, 2187-2193

Kazama, Toriyama (2016) PLOS ONE 11, 1-13

Toriyama, Kazama (2016) Rice 9, 1-4

Kazama et al (2016) Plant J 85, 707-716

Fujii et al (2014) Rice 7, 21

Kazama, Toriyama (2014) Rice 7, 28

Okazaki et al (2013) Plant Cell Physiol 54, 1560-1568

Igarashi et al (2013) Plant Cell Physiol 54, 237-243

Itabashi et al (2011) Plant J 65, 359-367

Fujii et al (2010) Plant Cell Physiol 51, 610-620

Fujii et al (2010) BMC Genomics 11, 209

Kojima et al (2010) Plant Biotechnol 27, 111-114

Fuji, Toriyama (2009) Proc Natl Acad Sci USA 106, 9513-9518

Fujii et al (2009) Plant Cell Physiol 50, 828-837

Itabashi et al (2009) Plant Cell Rep 28, 233-239

Fujii, Toriyama (2008) Plant Cell Physiol 49, 1484-1494

Kazama et al (2008) Plant J 55, 619-628

Fuji, Toriyama (2008) Plant Cell Physiol 49, 633-640

Fujii et al (2008) Biotechnol Agri Forestry 62, 205-215

Fujii et al (2007) Plant Mol Biol 63, 405-417

Fujii, Toriyama (2005) Theor Appl Genet 111,696-701

Kazama, Toriyama (2003) FEBS Lett 544, 99-102