Koshihikari: a premium short-grain rice cultivar – its expansion and breeding in Japan
- 1.2k Downloads
Koshihikari, a Japanese short-grain rice cultivar, was developed in 1956, more than 60 years ago. Despite its age, it has been the most widely grown cultivar in Japan for more than 35 years, making it the most important rice for the Japanese people. In its early days, there was no reason to predict that Koshihikari would become so widely disseminated. However, since the end of the post–World War II food shortage in the 1960s, Japanese preferences changed from high productivity to good eating quality. This triggered wide expansion of Koshihikari cultivation due to the cultivar’s excellent taste and texture. With increasing cultivation of Koshihikari in Japan, several good agronomic characteristics beyond its high eating quality became apparent, such as its good adaptation to different environments, tolerance to pre-harvest sprouting, and cold tolerance during the booting stage. These characteristics outweigh drawbacks such as its low blast resistance and low lodging resistance. The popularity of Koshihikari influenced subsequent rice breeding trends at regional agricultural experimental stations, and the characteristics of newly developed rice cultivars in Japan are usually rated relative to Koshihikari, which is used as the benchmark. Koshihikari was the first japonica rice cultivar whose whole genome has been sequenced by means of next-generation sequencing. Furthermore, comparison of the genomes of Koshihikari and Nipponbare has provided detailed insights into the genetic diversity of Japanese rice cultivars relative to that in rice populations elsewhere in the world. Further progress in rice genomics is gradually unlocking the mechanisms that underlie the agronomic characteristics of Koshihikari. To support both research and the development of novel rice cultivars, a series of isogenic and near-isogenic lines in the Koshihikari genetic background have been continuously developed. These new findings and materials will facilitate genomics-assisted rice breeding, eventually leading to superior cultivars.
KeywordsEating quality Koshihikari Marker-assisted breeding Quantitative trait locus Temperate japonica group
Backcross inbred line
Chromosome segment substitution line
Quantitative trait locus
Rice (Oryza sativa L.) is a staple food in Japan. It was introduced into Japan from China’s Yangtze river basin and downstream catchments about 2000 to 3000 years ago, and it has been cultivated throughout the country ever since (reviewed by Matsuo 1997, Tanaka et al. 2010). Cross-breeding of rice started in 1921 in Japan, and thousands of cultivars have since been developed. Among them, Koshihikari is the preferred cultivar of Japanese consumers.
Koshihikari, a premium short-grain rice cultivar, was bred in 1956. It became the cultivar with the largest cultivation area in 1979, and since then, has continuously maintained its top position in Japan. In 2016, Koshihikari was planted on about 535,000 ha, which amounts to 36.2% of the total paddy rice area (Rice Stable Supply Support Organization Website, Ministry of Agriculture, Forestry and Fisheries Website-1). The main reason for this widespread preference for Koshihikari by Japanese consumers is its superior eating quality. Japanese people prefer a sticky and chewy texture, and dislike a dry and crisp texture. Strong stickiness is one of its most important features (Tanaka et al. 2006, Takeuchi et al. 2008, Wada et al. 2008). On the other hand, Koshihikari has two serious defects: low resistance to both lodging and rice blast. To extend cultivation of Koshihikari to wider areas, it was necessary to overcome those defects while retaining its high eating quality. Therefore, many agricultural researchers have studied Koshihikari deeply in terms of its ecology, morphological characteristics, physiological functions, cultivation techniques, eating quality, physicochemical properties, and genomics.
By the end of the twentieth century, Koshihikari was also cultivated outside of Japan. In California, USA, Koshihikari was cultivated on about 400 ha in 1991 (Iwata 1992). In New South Wales, Australia, Koshihikari has been cultivated since 1991, and the paddy yield was very high, at about 13.7 t/ha (Ohnishi et al. 1993). Koshihikari is also accepted by Chinese consumers; for example, Koshihikari rice produced in Japan was sold for about 50 times the price of ordinary Chinese rice at a Chinese supermarket in 2007 (Lee et al. 2010, Ministry of Agriculture, Forestry and Fisheries Website-2). It has also been produced by organic farming methods in Yu Tai Xian, Shandong Province, China, since 2016. Though people expect high eating quality from Koshihikari in these areas, environmental conditions such as high temperature and low humidity tend to prevent it from achieving the same quality as in Japan (Iwata 1992, Kawamura et al. 1996). Despite these drawbacks, breeding, research, and selection to improve the eating quality of Koshihikari (again, used as the standard of comparison) have been done energetically in China (Lee et al. 2010, Liang et al. 2013, Sun et al. 2006). The high seedling establishment of Koshihikari under both low temperature and deep-sowing conditions prompted the proposal to improve the direct-seeding suitability of Cambodian rice by using Koshihikari (Tong et al. 2007), in spite of its long culm and low resistance to lodging.
Although breeders have tried to mitigate or eliminate the defects of Koshihikari using it in breeding programs to produce rice with high eating quality, no cultivar is more widely cultivated than Koshihikari in Japan. This seems to be due to Koshihikari’s high brand recognition and the conservative eating preferences of Japanese consumers. However, in recent years, several cultivars with different eating quality have been developed that are being gradually accepted by consumers. In this review, we look back on the breeding history, dissemination, and characteristics of Koshihikari, then summarize genetic studies of its agronomic traits, as well as some improvements in Koshihikari. We conclude with a discussion of the future prospects for going beyond Koshihikari.
Agricultural profile of Koshihikari
Breeding of Koshihikari
In 1956, the average paddy yield of Koshihikari ranged from 4940 to 5440 kg/ha according to an unpublished breeding report by the Fukui Agricultural Experiment Station. During the cultivar’s dissemination throughout Japan, many cultivation techniques have been developed to prevent lodging, increase yield, and retain the high eating quality. These include transplanting of younger seedlings to increase the duration of the growing season (Horiguchi et al. 1991); improving water management by allowing soil drying during growth to suppress excessive culm elongation; diagnosing growth problems using the culm length, leaf color, and culm number (Sasaki 1985, Ichimaru and Kanayama 1989); splitting the application of fertilizer during the reproductive stage (Matsuzaki et al. 1982, Ikeda and Kasai 1986, Sasaki 1985); and using growth regulators (Hashizume and Yamagishi 1969). As a result, the paddy yield of Koshihikari increased to 6630 kg/ha by 1985 in the Hokuriku region. Recently, delayed transplanting time (Yamaguchi et al. 2004, Morita et al. 2011) and the use of deep irrigation (Chiba et al. 2011) have been adopted to avoid heat-induced declines in the quality of rice kernels during the ripening period. Direct seeding of Koshihikari has been tried, but it has large disadvantages because it produces long culms and a higher lodging rate (Sakai et al. 2000, Sato and Sakai 2004).
Agronomic characteristics of Koshihikari
Japan covers a wide range of latitude, from 46°N to 20°N, so environmental characteristics such as day length and temperature vary widely among regions. Therefore, rice cultivars are usually chosen to fit the environment of each area. However, Koshihikari can be cultivated at latitudes ranging from 40°N to 31°N (Fig. 3). This high adaptability of Koshihikari originates from its heading properties. In addition, the basic vegetative growth duration of Koshihikari was 35.2 days when it was cultivated under short-day conditions after sprouting at 28 °C (Mimoto et al. 1989). This duration could be divided into the juvenile phase, when it is insensitive to the short-day conditions (13.1 days), and the reproductive phase until heading, when it is sensitive to photoperiod (22.1 days). Its temperature sensitivity is high (Hosoi 1979), and its photoperiod sensitivity is relatively weak compared with other Japanese rice cultivars (Mimoto et al. 1989, Hori et al. 2013).
It is noteworthy that the advantages of Koshihikari have gradually become clear during its dissemination throughout Japan. Its strong cold tolerance during the booting stage was identified in paddy fields irrigated with cold water in northern regions (Ozeki et al. 1995), and Hosoi (1989) found that this was relatively strong on the basis of the critical low temperature at which a cultivar is able to produce at least 80% of perfectly mature grains, although Koshihikari was selected without a prior evaluation for cold tolerance. This strong cold tolerance during the booting stage was inherited by Hitomebore and Akitakomachi (Fig. 1, Fig. 3); these cultivars have frequently resisted damage from cold weather in northern regions of Japan.
Koshihikari’s strong tolerance to pre-harvest sprouting was revealed in the southern Kyushu region, where harvesting sometimes occurs during the rainy season (early July). This trait has also been very helpful in Hokuriku, where rice is also harvested during the rainy season (September) (Ishizaka et al. 1989).
High eating quality is one of the major reasons why Koshihikari is preferred by Japanese consumers. The eating quality of Koshihikari is superior to that of Nipponbare, a standard rice, in appearance, scent, flavor, stickiness, and overall evaluation, and cooked Koshihikari rice is much softer than Nipponbare (Takeuchi et al. 2008). Its eating quality was evaluated as the highest among 112 cultivars in Japan (Yamamoto and Ogawa 1992). The amylose content of Koshihikari is relatively low (Koike et al. 1993); in Fukui Prefecture from 1994 to 2007, it averaged 17.2%, versus average of 19.4% for Nipponbare. Cooked rice grains of Koshihikari show strong stickiness (Tanaka et al. 2006, Kobayashi et al. 2008, Takeuchi et al. 2008, Wada et al. 2008). This feature has been inherited by other Japanese rice cultivars such as Hitomebore and Akitakomachi that are progeny of Koshihikari (Fig. 1).
Nevertheless, Koshihikari has disadvantages. Its lodging resistance was rated as ‘very weak’ (Takaya and Miyasaka 1981, Terashima et al. 1992) owing to its long culm and its low breaking strength (Ookawa and Ishihara 1992). Its blast resistance in the field was rated as ‘weak’ for leaf blast and ‘slightly weak’ for panicle blast (Ishizaka et al. 1989); although Koshihikari has some resistance genes, including Pish and Pik-s, blast races virulent against Pish and Pik-s are distributed widely in Japan (Kawasaki-Tanaka and Fukuta 2014, Kawasaki-Tanaka et al. 2016). It is susceptible to the leaf stripe virus and shows slightly strong resistance to bacterial leaf blight (Ishizaka et al. 1989, Ogawa et al. 1998). Koshihikari has medium incidence of bacterial brown stripe disease (Kadota and Ohuchi 1989). In addition, with global warming, average dairy minimum temperature from June to August has increased by about 1.1 °C from 1966 to 2001 (Kawatsu et al. 2007), and temperature during ripening period has also increased by 1.1 °C above that in past years (Sugiura et al. 2013). Therefore, a heat-induced decline in the quality of Koshihikari has been observed in many prefectures (Sugiura et al. 2013, Inoue 2012).
Progeny of Koshihikari
Rice cultivation in 2016 in Japan (source: Rice Stable Supply Support Organization website)
Hitomebore/Kukei 90242A//Kuiku 150
Shu 2800/Hokuriku 100//Hokuriku 96
Ouu 341/Yamagata 40
Asahi no yume
Aichi 70//Aichi 56/Aichi 65
Satsukei 96118/Jouiku 427
Koshihikari is a valuable genetic resource for good eating quality, but its long culm and susceptibility to rice blast disease have often caused difficulty for its use as a parent. To compensate for these disadvantages, mutation and backcross breeding of Koshihikari have been used frequently. At present, 29 cultivars have been developed by mutation of Koshihikari (National Agriculture and Food Research Organization Website). Hokuriku 100, a semi-dwarf mutant of Koshihikari, was bred by means of gamma-ray mutation, and has a 30% shorter culm length than Koshihikari (Tanisaka et al. 1990). Jikei 58 was selected from protoplast-derived plants of Koshihikari, and has a 20% shorter culm length (Noda et al. 1997). Mutations for the physicochemical components of kernel quality of Koshihikari have also been selected. A dull-white mutant, Milky Queen, was selected from the progeny after treatment of Koshihikari with N-methyl-N-nitrosourea; it has a lower amylose content (9% to 12%) in the endosperm than Koshihikari (17.5%) (Ise et al. 2001). Yumegokochi was selected from the progeny of protoplast-derived plants of Koshihikari and also has a 1.5% lower amylose content (Sukekiyo et al. 1995). Using gamma-ray mutation, rice cultivars have been bred that lack alpha-globulin protein (Iida et al. 1998, Nishimura et al. 2005), and a strong culm (Samoto and Kanai 1975). A novel cultivar with low cadmium levels in its endosperm, Koshihikari Kan No. 1, was selected from mutations induced by ion-beam irradiation (Ishikawa et al. 2012, Abe et al. 2017).
At present, 55 isogenic and near-isogenic lines (NILs) of Koshihikari have been developed (National Agriculture and Food Research Organization Website). Notably, blast-resistant NILs possessing one or more R-genes in the Koshihikari genetic background were developed: Kojima et al. (2003) developed six NILs in Toyama Prefecture; Ishizaki et al. (2005) developed 12 NILs in Niigata Prefecture. Seeds of these NILs are now mixed in a ratio that is determined from disease forecasts by field pathologists, and are provided to the farmers as a BL series (i.e., blast-resistant lines) every year. Accessions in the BL series are designated as lines that belong to the Koshihikari brand. About 88,000 ha of cultivation of these accessions throughout Niigata Prefecture has decreased the occurrence of rice blast, and this has let farmers reduce pesticide use by 25% (Ishizaki et al. 2005, Niigata Prefecture Website). To increase lodging resistance, backcross breeding to incorporate one or more semi-dwarfing genes has been carried out at several universities and local rice research institutes (Nonaka et al. 1991, Murai and Endo 2006, Tomita 2009). However, these cultivars have not replaced the original Koshihikari in most places, because some skillful farmers have resolved the lodging problem and prioritize current Koshihikari over “semi-dwarf” Koshihikari.
Genomics of Koshihikari
Genome resequencing and haplotype inheritance
The rice genome sequence was decoded in 2005 (IRGSP 2005). After this breakthrough, many of the agriculturally important genes were identified by advanced research institutes around the world. In parallel, researchers have aimed to understand the breeding history and characteristics of Koshihikari by using DNA markers.
Yamamoto et al. (2010) determined the whole-genome sequence of Koshihikari by using next-generation sequencing. Though the average short read length of next-generation sequencing was 30 to 35 base pairs, these authors aligned the reads and completed a pseudomolecule of Koshihikari by using the Nipponbare genome sequence as a reference. They estimated 67,051 single-nucleotide polymorphisms (SNPs) between these two cultivars. A GoldenGate typing array consisting of 1917 SNPs extracted from this total revealed genome-wide polymorphisms in 151 Japanese cultivars. By comparing the polymorphism information with pedigree records of rice breeding in Japan, Yamamoto et al. (2010) identified the ancestral origin of the pedigree haplotypes in 60.9% of the Koshihikari genome. Furthermore, they identified 28.6% of Koshihikari’s ancestral landraces. The proportion of the Koshihikari genome inherited by three of its famous progeny―Hitomebore, Akitakomachi, and Hinohikari―was 80.8, 80.0, and 61.3%, respectively. In addition, 18 pedigree haplotypes were inherited from landraces and shared among Koshihikari and these three progeny, which together account for 61.9% of the total cultivated area in Japan (Table 1).
As we noted in the previous section, rice breeders tend to use Koshihikari and select phenotypes, especially for good eating quality, that resemble it. This may explain the wide dissemination of Koshihikari’s genome, which suggests the low frequency of DNA polymorphisms among recent Japanese cultivars. However, information on the large number of SNPs obtained from the whole-genome sequence overcame this inefficiency of DNA marker development, and has accelerated the detection of agronomically important quantitative trait loci (QTLs).
QTL analysis in experimental populations
Detection of QTLs is a primary step in efforts to understand the genetic basis for agronomic traits, because many agronomic traits are generally controlled by multiple QTLs. To identify the QTLs involved in the control of agronomically important traits in Koshihikari and Nipponbare, researchers have developed two types of segregating populations—backcross inbred lines (BILs) and chromosome segment substitution lines (CSSLs)—from reciprocal crosses between the two cultivars (Matsubara et al. 2008, Hori et al. 2010).
A QTL for good eating quality in Koshihikari was detected on the short arm of chromosome 3 (Takeuchi et al. 2008, Hori and Yano 2013). Other genetic studies have found major-effect QTLs for eating quality traits by using segregating populations derived from crosses with Koshihikari (Takeuchi et al. 2007, Kobayashi et al. 2008, Wada et al. 2008). Fine-mapping of a seed dormancy QTL revealed that a nonfunctional qLTG3–1 allele, was associated with strong tolerance to pre-harvest sprouting in Koshihikari (Hori et al. 2010). A novel QTL on the short arm of chromosome 1 (qCL1) was associated with long culm length and weak lodging resistance in Koshihikari (Hori et al. 2009, Hori et al. 2012). A QTL for strong cold tolerance at the booting stage (qCT7) was detected on the long arm of chromosome 7 (Takeuchi et al. 2001, Hori et al. 2017). Fukuoka et al. (2010) and Hori et al. (2017) detected and validated the QTL for leaf blast resistance (qLBR1) on the short arm of chromosome 1. This QTL allele in Koshihikari conferred susceptibility to leaf blast infection. These QTLs contributed strongly to agronomic characteristics in Koshihikari.
Marker-assisted breeding for “pinpoint” improvement of Koshihikari
To increase the agronomic value of Koshihikari, many researchers have tried to introduce new genes from diverse genetic resources into it. Several series of CSSLs using Koshihikari as the recurrent parent have contributed greatly to this research (Ebitani et al. 2005, Takai et al. 2007, Takai et al. 2014, Abe et al. 2013, Murata et al. 2014, Nagata et al. 2015). Because a large amount of information about the environmental responses of Koshihikari has accumulated, a small but stable effect on a target trait can be accurately evaluated. This means that breeders who use Koshihikari can take advantage of high-resolution marker-assisted breeding (“pinpoint” improvement) by using NILs. Some CSSLs have been derived from wild relatives such as Oryza rufipogon, O. glumaepatula, and O. nivara (Hirabayashi et al. 2010, Furuta et al. 2014, Furuta et al. 2016). Ashikari et al. (2005) detected QTLs for grain number and culm length from a high-yielding indica cultivar in the Koshihikari genetic background, and introduced them into Koshihikari to create a new line with both high yield and higher lodging resistance.
Since this successful QTL pyramiding, many trials of pinpoint improvement of Koshihikari have been reported (category A in Additional file 1: Table S1). Though the target QTLs were not cloned, their phenotypic effects in the Koshihikari genetic background have been evaluated and incorporated in actual breeding programs (categories B and C in Additional file 1: Table S1). In addition to successful trials of a Koshihikari BL series (Ishizaki et al. 2005) described earlier in this paper, improvement of panicle blast resistance (Sugiura et al. 2004) and development of a semi-dwarf phenotype (Wang et al. 2005) were also achieved by using DNA markers. However, pinpoint improvement of other agronomic traits, especially yield-related traits, is still in progress or under evaluation. This work has not encountered significant technical problems, but the improved cultivars have not always proven to be acceptable to Japanese farmers or consumers. Some problems, such as tight linkage, pleiotropy or introgression out of the target region, need to be overcome. The incredibly strong power of the Koshihikari brand has been a major barrier to dissemination of these new cultivars, even though they are NILs of Koshihikari.
Future perspectives for Koshihikari research
Table 1 shows the continuing preference of Japanese consumers for cooked Koshihikari rice: the top five cultivars were developed more than 15 years ago, and Koshihikari-like sticky rice has been loved since the 1950s. However, Japanese rice consumption has been decreasing since the 1970s, by 80 kt per year (Rice Stable Supply Support Organization Website). This has resulted from Japan’s decreasing population, which has resulted from a declining birthrate and the aging population, and has been exacerbated by a transition to increased consumption of wheat products such as bread. Furthermore, there has been increasingly wide diversification of the eating quality of cooked rice in Japan. For example, younger Japanese tend to prefer harder cooked rice rather than sticky rice like Koshihikari according to recent market research (Fukui Prefecture, unpublished data). To meet these demands, Japanese rice breeders have tried to develop new cultivars that can increase rice consumption and respond to the diversification of eating quality preferences.
One solution has been the development of rice with different eating qualities from Koshihikari. For example, Ichihomare (Kobayashi et al. 2017), Shinnosuke (Kasaneyama et al. 2017), and Tsuyahime (Asanome et al. 2010) have a somewhat hard surface in the cooked rice and are being accepted as a new type of rice by consumers. In contrast, Yumepirika (Yoshida et al. 2013) and Pikamaru (Sakai et al. 2016) have a low amylose content (16.1% and about 10%, respectively) and their cooked rice is stickier than Koshihikari. In addition, the appearance of cooked rice is one of the most important characteristics for judgments of eating quality (Oosato et al. 1998, Shigemune et al. 2007). Objective measurements of the whiteness of cooked rice have been obtained using a spectrophotometer (Goto et al. 2014) or by means of image analysis (Kogi et al. 2014). A few cultivars are whiter and glossier than Koshihikari (Machida et al. 2017).
About 30% of rice consumption is accounted for by take-home rice from supermarkets and eating in restaurants (Rice Stable Supply Support Organization Website). Unique properties are needed for rice that is processed by large-scale rice cooking systems in factories; these include a somewhat hard surface for the cooked rice, a volume increase after cooking, slower degradation during refrigerated transport, and suitability for blending with other rice cultivars; unfortunately, these properties are not provided by Koshihikari rice. Recently, several Japanese rice breeding projects have attempted to develop cultivars with such properties to support industrial uses. These projects have been started by the National Agriculture and Food Research Organization and prefectural governments to meet current and future demands.
Another solution is “healthy” rice. Recently, health consciousness has been increasing in Japan. Researchers have tried to take advantage of Koshihikari’s good eating quality while adding functionality. Idesawa et al. (2017) selected a line that has 2 to 3.1 times the content of dietary fiber in the endosperm of Koshihikari using progeny derived from gamma-irradiation. Black (Maeda et al. 2014) and red (Yamaguchi et al. 2015) rice contain anthocyanins and tannins (both healthful nutraceuticals), respectively, and these cultivars were developed using Koshihikari as a recurrent parent. A mutant line of Koshihikari that was deficient in a 26-kDa globulin was used to develop cultivars, with a low content of easy-to-digest protein (Iida et al. 1998, Nishimura et al. 2005).
Breeders have continued to develop new rice varieties whose properties surpass those of Koshihikari. Scientists have continued to elucidate the secrets of Koshihikari’s genome. Farmers have continued to provide delicious rice, including both Koshihikari and cultivars with different characteristics that meet the demands of consumers. Such sincere and large-scale efforts will continue, leading to sustainable rice production in Japan’s paddy fields.
Despite weak resistance to blast diseases and lodging susceptibility, Japanese farmers have learned to successfully cultivate Koshihikari by applying their practical skills, leading to widespread adoption of Koshihikari. Japanese manufacturers have also been involved in rice cultivation, processing, and cooking to adapt their products to use Koshihikari. In addition, the spread of Japanese food restaurants outside of Japan has accelerated demand for rice with high eating quality. These trends have increased the value of Koshihikari and Koshihikari-like rice. For these reasons, rice-using industries, scientists, and consumers can’t discuss Japanese rice without thinking of Koshihikari.
However, the dominance of Koshihikari or its genome caused by excessive reliance on this cultivar has not always been beneficial for rice in Japan. As the national demographic structure and Japanese lifestyles and preferences change, the nature of the demand for rice is also changing. It is also necessary to prepare a broader range of genetic materials to protect against both expected and unexpected environmental changes, such as global warming, soil degradation, and typhoons. The rapid decrease in the number of farmers is a serious social concern in Japan, and suggests a need for rice that can be cultivated more easily by the remaining farmers. For all these reasons, development of rice cultivars with high and sustainable yield, combined with low cultivation costs, is an urgent breeding objective. In this context, improving our understanding of the genetic basis of Koshihikari’s agronomic characteristics, followed by comprehensive utilization of this knowledge for genetic improvement, will be more important than ever before.
The authors wish to thank Mr. Katsura Tomita (Fukui Agricultural Experiment Station) and Dr. Kazuhiko Ishizaki (Niigata Agricultural Research Institute) for providing historical information about breeding of Koshihikari, Dr. Ryuji Ishikawa (Hirosaki University) for providing historical information of origin of Japanese rice, and the Ministry of Agriculture, Forestry and Fisheries of Japan for financial support conducting genomics research of Koshihikari.
Availability of data and materials
The datasets supporting the conclusions of this paper are included within the article (and its Aditional file).
TY developed the overall concept of this review. AK, KH and TY contributed in organizing the content and writing the different sections of the manuscript. MY reviewed the draft and provided critical scientific inputs for the improvement of the manuscript. All of the authors read and approved the final manuscript.
Ethics approval and consent to participate
Consent for publication
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
- Asanome N, Moriya M, Suzuki K (2010) Eating quality evaluation of new rice variety ‘Tsuyahime’ III. Eating quality analysis by multipronged physical evaluation. Jpn J Crop Sci 79(Suppl 2):152–153 (in Japanese)Google Scholar
- Chiba M, Matsumura O, Terao T, Takahashi Y, Watanabe H (2011) Effect of deep planting and deep-flood irrigation on the yield and quality of rice. Jpn J Crop Sci 80:312–325 (in Japanese with English summary)Google Scholar
- Ebitani T, Takeuchi Y, Nonoue Y, Yamamoto T, Takeuchi K, Yano M (2005) Construction and evaluation of chromosome segment substitution lines carrying overlapping chromosome segments of indica rice cultivar ‘Kasalath’ in a genetic background of japonica elite cultivar ‘Koshihikari. Breed Sci 55:65–73CrossRefGoogle Scholar
- Fukui Prefectural Government (1995) Brief descriptions of the Japanese leading rice variety, ‘Koshihikari’, and its lineage. In: Proceeding of ‘2nd Asian Crop Science Conference’, pp 2–3Google Scholar
- Fukuoka S, Saka N, Mizobuchi R, Hori K, Yano M (2010) QTL analysis for field resistance to blast using Nipponbare/Koshihikari backcross inbred and chromosome segment substitution lines in rice. Breed Res 12(Suppl 1):171 (in Japanese)Google Scholar
- Furuta T, Uehara K, Angeles-Shim RB, Shim J, Ashikari M, Takashi T (2014) Development and evaluation of chromosome segment substitution lines (CSSLs) carrying chromosome segments derived from Oryza rufipogon in the genetic background of Oryza sativa L. Breed Sci 63:468–475CrossRefPubMedPubMedCentralGoogle Scholar
- Hashizume A, Yamagishi A (1969) Studies on growth regulation of rice plants by soil treatment with pentachlorophenol (PCP). I Effect of PCP on controlling over-growth and lodging of rice plants in ill-drained paddy field. Jpn J Crop Sci 38:388–395 (in Japanese with English summary)CrossRefGoogle Scholar
- Hirabayashi H, Sato H, Nonoue Y, Kuno-Takemoto Y, Takeuchi Y, Kato H, Nemoto H, Ogawa T, Yano M, Imbe T et al (2010) Development of introgression lines derived from Oryza rufipogon and O. glumaepatula in the genetic background of japonica cultivated rice (O. sativa L.) and evaluation of resistance to rice blast. Breed Sci 60:604–612CrossRefGoogle Scholar
- Hori K, Sugimoto K, Nonoue Y, Ono N, Matsubara K, Yamanouchi U, Abe A, Takeuchi Y, Yano M (2010) Detection of quantitative trait loci controlling pre-harvest sprouting resistance by using backcrossed populations of japonica rice cultivars. Theor Appl Genet 120:1547–1557CrossRefPubMedPubMedCentralGoogle Scholar
- Hori K, Yano M (2013) Genetic improvement of grain quality in japonica rice. In: Varshney RK, Yuberosa R (eds) Translational genomics for crop breeding Vol. II abiotic stress, yield and quality, Wiley Blackwell, Iowa, USA, pp 143–160Google Scholar
- Horiguchi K, Onishi I, Nakamura M, Hokoyama K (1991) Prolongation of harvesting time by changing the transplanting date in paddy rice ‘Koshihikari’. Bull Shiga Pref Agri Exp Stn 32:75–79 (in Japanese)Google Scholar
- Hosoi N (1979) Studies on meteorological fluctuation in the growth of rice plants. III. Relation between the heading response of rice varieties to temperature under natural daylength and the thermos-sensitivity, photo-sensitivity, basic vegetative growth under controlled environments. Jpn J Breed 29:294–304 (in Japanese with English summary)CrossRefGoogle Scholar
- Ichimaru Y, Kanayama H (1989) Growth diagnosis of the early-season rice cultivar ‘Koshihikari’ at the Uwaba district in Saga prefecture. Rep Kyushu Br Crop Sci Soc 56:28–30 (in Japanese)Google Scholar
- Idesawa Y, Tanimoto R, Oyamada M, Komiya U, Nishimura M (2017) Screening and evaluation of high dietary fiber mutants in rice seeds. Breed Res 19(Suppl 1):48 (in Japanese)Google Scholar
- Iida S, Miyahara K, Nishio T (1998) Rice mutant lined lacking α-globulin. Breed Sci 48:45–49Google Scholar
- Ikeda T, Kasai H (1986) Effect of topdressing to deeper layer on growth and yield components of rice cultivar ‘Koshihikari’. 1. In case of changing ratio of amount of basal dressing to that of deeper layer to transplanted rice plants. Hokuriku Crop Sci 21:5–8 (in Japanese)Google Scholar
- Inoue K (2012) A technical attempt to avoid the high temperature damage during ripening on rice cultivar Koshihikari in Fukui prefecture –focusing on the transplanting time and grain qualities-. Hokuriku. Crop Sci 47:137–140 (in Japanese)Google Scholar
- Ise K, Akama Y, Horisue N, Nakane A, Yokoo M, Ando I, Hata T, Sito M, Numaguchi K, Nemoto H et al (2001) ‘Milky queen’, a new high-quality rice cultivar with low amylose content in endosperm. Bull Natl Inst Crop Sci 2:39–61 (in Japanese with English summary)Google Scholar
- Ishikawa S, Ishimaru Y, Igura M, Kuramata M, Abe T, Senoura T, Hase Y, Arao T, Nishizawa N, Nakanishi H (2012) Ion-beam irradiation, gene identification, and marker-assisted breeding in the development of low-cadmium rice. Proc Natl Acad Sci U S A 109:19166–19171CrossRefPubMedPubMedCentralGoogle Scholar
- Ishizaka S, Uehara Y, Fujita Y, Okuno K, Horiuchi H, Miura K, Nakagahra M, Yamada T, Uchiyamada H, Samoto S et al (1989) Breeding process and characteristic of new released variety Kinuhikari. Hokuriku Crop Sci 24:25–27 (in Japanese)Google Scholar
- Iwata T (1992) A report on a japonica rice variety ‘Koshihikari’ cultivated in foreign countries. Hokuriku Crop Sci 27:90–93 (in Japanese)Google Scholar
- Kadota I, Ohuchi A (1989) A method for testing varietal resistance to bacterial brown stripe of rice, caused by Pseudomonas avenae Manns 1909. Proc Ass Plant Prot Hokuriku 37:8–11 (in Japanese)Google Scholar
- Kasaneyama H, Hashimoto N, Kanbe T, Ishibashi T, Ishizaki K, Kobayashi K, Kaneda S, Matsui T, Nabata K, Nara E (2017) Breeding of late maturing new rice cultivar ‘Shinnosuke’ with excellent eating quality and strong tolerance to high-temperature during ripening period. Breed Res 19(Suppl 1):146 (in Japanese)Google Scholar
- Kobayashi A, Tomita K, Machida Y, Nakaoka F, Morozumi Y, Hayashi T, Tanoi M, Watanabe K, Sakai K, Shimizu T (2017) Breeding of a new rice cultivar ‘Ichihomare’. Breed Res 19(Suppl 2):116 (in Japanese)Google Scholar
- Koike H, Arai T, Tezuka M, Maejima H, Sakai N, Nakazawa N (1993) Studies on physicochemical properties of major rice varieties in Nagano. 1. Studies on physicochemical properties of good eating quality varieties. Hokuriku Crop Sci 28:15–17 (in Japanese)Google Scholar
- Kojima Y, Ebitani T, Kaneda H, Doi M, Ishibashi T, Kidani Y, Mukaino N, Yamaguchi T, Omoteno M, Yamamoto Y (2003) Development and utilization of isogenic lines Koshihikari Toyama. I. Development of isogenic lines Koshihikari Toyama BL. Bull Toyama Agri Res Ctr 20:13–31 (in Japanese with English summary)Google Scholar
- Lee JR, Zhang JM, Wang H, Li MB, Piao Z (2010) Differences in amylopectin structure and grain quality of rice between some high-quality japonica cultivars from the lower Yangtze river region, China and Koshihikari from Niigata, Japan. Chin J Rice Sci 24:379–384 (in Chinese with English summary)Google Scholar
- Liang CG, Zhang Q, Li J, Xiong D, Xu GL, Wang Y, Liu Q, Huang P, Li T (2013) Effect of high temperature on aspartate metabolism enzyme activities and aspartate-family amino acids contents at rice grain-filling stage. Chin J Rice Sci 27:71–76Google Scholar
- Matsubara K, Kono I, Hori K, Nonoue Y, Ono N, Shomura A, Mizubayashi T, Yamamoto S, Yamanouchi U, Shirasawa K et al (2008) Novel QTLs for photoperiodic flowering revealed by using reciprocal backcross inbred lines from crosses between japonica rice cultivars. Theor Appl Genet 117:935–945CrossRefPubMedGoogle Scholar
- Matsuo T (1997) Origin and differentiation of cultivated rice. In: Matsuo T, Futsuhara Y, Kikuchi F, Yamaguchi H (eds) Science of the Rice Plant, vol 3. Food and Agriculture Policy Research Center, Tokyo, pp 69–88Google Scholar
- Matsuzaki A, Kariya K, Machida H, Tsunoda K, Nishikawa Y (1982) Studies on the growth control and the nutritional diagnosis in rice plants. III Growth diagnosis at the stage of spikelet initiation for nitrogen top dressing. Jpn J Crop Sci 51:325–331 (in Japanese with English summary)CrossRefGoogle Scholar
- Mimoto H, Yanase M, Chujo H (1989) Varietal differences of juvenile phase duration and photoperiodic sensitivity in paddy rice. Jpn J Crop Sci 58:628–634 (in Japanese with English summary)Google Scholar
- Ministry of Agriculture, Forestry and Fisheries Website-1, http://www.e-stat.go.jp/SG1/estat/GL08020103.do?_toGL08020103_&listID=000001172509&requestSender=dsearch (in Japanese) Accessed 11 Sept 2017
- Ministry of Agriculture, Forestry and Fisheries Website-2, http://www.maff.go.jp/j/shokusan/export/e_enkatu/pdf/h23_china_2_2.pdf. (in Japanese) Accessed 11 Sept 2017
- Murai M, Endo Y (2006) A new rice cultivar ‘Hikarikko’: genes for short culm and earliness were introduced into ‘Koshihikari’ by backcrossing. Breed Res 8:183–189 (in Japanese)Google Scholar
- Nagata K, Ando T, Nonoue Y, Mizubayashi T, Kitazawa N, Shomura A, Matsubara K, Ono N, Mizobuchi R, Shibaya T, Ogiso-Tanaka E, Hori K, Yano M, Fukuoka S (2015) Advanced backcross QTL analysis reveals complicated genetic control of rice grain shape in a japonica × indica cross. Breed Sci 65:308–318CrossRefPubMedPubMedCentralGoogle Scholar
- National Agriculture and Food Research Organization Website, http://ineweb.narcc.affrc.go.jp/ (in Japanese) Accessed 11 Sept 2017
- Niigata Prefecture Website, http://www.pref.niigata.lg.jp/nosanengei/1215712857692.html (in Japanese) Accessed 11 Sept 2017
- Noda H, Teramoto K, Taniguchi S, Kohara Y, Mori M, Kitamura H, Watanabe K (1997) Studies on breeding using protoplast-derived plants in rice (Oryza sativa L.), Koshihikari variety III. Characteristics of semidwarf line ‘Jikei 58’ selected from the mutants. Bull Shiga Agr Exp Stn 38:17–24 (in Japanese with English summary)Google Scholar
- Nonaka K, Takagi Y, Mathuyuki S, Yokoh H, Hirota Y, Shigyo T, Shigetomi O, Kishikawa H, Nakayama D, Kanayama H et al (1991) A new rice cultivar ‘Saga 1 Gou’. Bull Saga Pref Agr Exp Stn 1-19:27 (in Japanese with English summary)Google Scholar
- Ogawa T, Endo N, Busto GA Jr, Tabien RE, Taura S, Khush GS (1998) Data set on the variety group resistant to bacterial leaf blight in rice. ― the variation of characteristics in the varietal differentiation of rice ― research report on agricultural development in the Hokuriku area. Res Rep Agric Dev Hokuriku Area 40:1–49Google Scholar
- Ohnishi M, Angus JF, Lewin L, Horie T (1993) A comparison of the growth and yield of Japanese and Australian rice cultivars at Yanco in Australia. Jpn J Crop Sci 62(Suppl 1):48–49 (in Japanese)Google Scholar
- Ozeki M, Sasaki Y, Kondo T (1995) Comparison of sterility by cool damage due to floral impotency within rice varieties in Niigata prefecture. Hokuriku Crop Sci 30:13–14 (in Japanese)Google Scholar
- Rice Stable Supply Support Organization Website, http://www.komenet.jp/jishuchousa/144.html. (in Japanese) Accessed 11 Sept 2017
- Sakai M, Tamura K, Kaji R, Tamura Y, Kataoka T, Sato H (2016) ‘Pikamaru’, a high yielding rice cultivar with low amylose content of grain for western region of Japan. Breed Res 18:152–157 (in Japanese)Google Scholar
- Sakai N, Saito M, Taniguchi T, Tuchiya M, Nakazawa K, Yanagisawa K, Fujisawa K, Sodeyama E (2000) Growth and yield of Koshihikari on direct hill-seeding combined pudding with seeding operation. Hokuriku Crop Sci 35:41–43 (in Japanese)Google Scholar
- Sasaki Y (1985) Problems and technical measures of high quality rice production at Niigata prefecture. Hokuriku Crop Sci 20:59–69 (in Japanese)Google Scholar
- Sato T, Sakai K (2004) Studies on rice [Oryza sativa] direct sowing cultivation under flooded paddy field, 2: High yielding cultivation of Koshihikari by improving seedling establishment and utilizing growth index at panicle formation stage. Bull Fukui Agr Exp Stn:39–45 (in Japanese with English summary)Google Scholar
- Sugiura N, Tsuji T, Fujii K, Kato T, Saka N, Touyama T, Hayano-Saito Y, Izawa T (2004) Molecular marker-assisted selection in a recurrent backcross breeding for the incorporation of resistance to rice stripe virus and panicle blast in rice (Oryza sativa L.) Breed Res 6:143–148 (in Japanese)CrossRefGoogle Scholar
- Sukekiyo Y, Hayashi Y, Yahiro Y (1995) Production of a unique rice variety ‘Yumegokochi’ by protoplast breeding method and its application for commercial use. Research J Food and Agric 26:44–47 (in Japanese)Google Scholar
- Sun SY, Hao W, Lin HX (2006) Identification of QTLs or cooking and eating quality of rice grain. Rice Sci 13:161–169Google Scholar
- Takai T, Ikka T, Kondo K, Nonoue Y, Ono N, Arai-Sanoh Y, Yoshinaga S, Nakano H, Yano M, Kondo M et al (2014) Genetic mechanisms underlying yield potential in the rice high-yielding cultivar Takanari, based on reciprocal chromosome segment substitution lines. BMC Plant Biol 14:295CrossRefPubMedPubMedCentralGoogle Scholar
- Takai T, Nonoue Y, Yamamoto SI, Yamanouchi U, Matsubara K, Liang ZW, Lin HX, Ono N, Uga Y, Yano M (2007) Development of chromosome segment substitution lines derived from backcross between indica donor rice cultivar ‘Nona bokra’ and japonica recipient cultivar ‘Koshihikari’. Breed Sci 57:257–261CrossRefGoogle Scholar
- Tanisaka T, Tomita M, Yamagata H (1990) Gene analysis for the semidwarfism of two mutant strains, Hokuriku 100 and Kanto 79, induced from a rice variety Koshihikari: studies on the utility of artificial mutations in plant breeding XVIII. Jpn J Breed 40:103–111 (in Japanese with English summary)CrossRefGoogle Scholar
- Wang ZX, Sakaguchi S, Oka Y, Kitazawa N, Minobe Y (2005) Breeding of semi-dwarf Koshihikari by using genome breeding method. Breed Res 7(Suppl 1.2):217 (in Japanese)Google Scholar
- Yamaguchi T, Omoteno M, Maeda H, Morikawa M, Kidani Y, Ozaki H, Murata K, Iyama Y, Kojima Y, Takarada T et al (2015) Development of a new rice cultivar named ‘aka-Musubi’. Bull Toyama Agric Res Inst 6(in Japanese with English summary):9–26Google Scholar
- Yamaguchi Y, Inoue K, Yuasa K (2004) Effects of the transplanting time on dry matter production, yield and grain appearance in rice cultivar Koshihikari during high temperature years. Bull Fukui Agr Exp Stn 41:29–38 (in Japanese with English summary)Google Scholar
- Yoshida S, Nagata T, Igarashi T, Sasaki T (2013) Prediction of amylose contents of ‘Yumepirika’, Hokkaido low-amylose rice cultivar, before harvest season I. Jpn J Crop Sci 82(suppl 2):194–195 (in Japanese)Google Scholar
Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.