Skip to main content
Log in

Utilizing the genetic diversity within rice cultivars

  • Emerging Technologies
  • Published:
Planta Aims and scope Submit manuscript

Abstract

Plant breeding of rice emphasizes improvement in yield, disease resistance, and milling quality. Numerous other traits (e.g., bran carotenoids) that historically have not been selected for could provide added value in expanding niche markets, as well as be useful tools for understanding the genetic control of these traits. Residual heterozygosity is present in many rice cultivars; therefore, it is possible to select for different alleles within an existing cultivar. By identifying and using cultivars with high levels of variability for a trait, we were able to develop separate lines from single cultivars that showed high and low levels of that trait. The rice cultivar RU9101001 and the warm- and cold-sprouting lines that were derived from it were used to demonstrate that residual heterozygosity was present within a cultivar and that the original heterozygosity was separated in the derived lines. Rice simple sequence repeat markers were heterozygous in the parent RU9101001 cultivar, but the cold-sprouting lines were homozygous for one set of alleles and the warm-sprouting lines were homozygous for the other set. Through detailed phenotypic screening, we developed lines that exhibited low and high levels of the following traits in the specified cultivars: cold-sprouting from RU9101001 and Bonnet 73, postharvest yellowing from Tominishiki, early tillering from Hei Jaio and Tominishiki, and bran carotenoid levels from Spring. If variability exists in a cultivar, then utilization of residual heterozygosity may provide a quicker and more efficient means to develop lines with special characteristics using cultivars that are already agronomically valuable or to develop near isogenic lines for genetic and biochemical investigations.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Fig. 1
Fig. 2
Fig. 3
Fig. 4
Fig. 5

Similar content being viewed by others

Abbreviations

NIFI:

Net integrated fluorescence intensity

NILs:

Near isogenic lines

PHY:

Postharvest yellowing

RFLP:

Restriction fragment length polymorphism

RILs:

Recombinant isogenic lines

SSLP:

Simple sequence length polymorphisms

SSR:

Simple sequence repeat

References

  • Agrama HA, Yan W (2009) Association mapping of straighthead disorder induced by arsenic in Oryza sativa. Plant Breed 128:551–558

    Google Scholar 

  • Allard RW (1960) Principles of plant breeding. Wiley, NY

    Google Scholar 

  • Baruah AR, Ishigo-Oka N, Adachi M, Oguma Y, Tokizono Y, Onishi K, Sano Y (2008) Cold tolerance at the early growth stage in wild and cultivated rice. Euphytica 165:459–470

    Google Scholar 

  • Belefant-Miller H (2007) Poultry litter induces tillering in rice. J Sustain Agric 31:151–160

    Google Scholar 

  • Belefant-Miller H (2009) Induced postharvest yellowing in southern U.S. rice cultivars. Cereal Chem 86:67–69

    CAS  Google Scholar 

  • Belefant-Miller H, Grace SC (2010) Variations in bran carotenoids levels within and between rice subgroups. Plant Foods Hum Nutr 65:358–363

    PubMed  CAS  Google Scholar 

  • Belefant-Miller H, Kay MG, Lee FN (2005a) Small-scale induction of postharvest yellowing of rice endosperm. Cereal Chem 82:721–726

    CAS  Google Scholar 

  • Belefant-Miller H, Miller GH, Rutger JN (2005b) Nondestructive measurement of carotenoids in plant tissues by fluorescence quenching. Crop Sci 45:1786–1789

    CAS  Google Scholar 

  • Brandolini V, Tedeschi P, Cereti E, Maietti A, Barile D, Coisson JD, Mazzotta D, Arlorio M, Martelli A (2005) Chemical and genomic combined approach applied to the characterization and identification of Italian Allium sativum L. J Agric Food Chem 53:678–683

    PubMed  CAS  Google Scholar 

  • Briggs FN, Knowles PF (1967) Introduction to plant breeding. Reinhold Publ, New York

    Google Scholar 

  • Cho YG, McCouch SR, Kuiper M, Kang MR, Pot J, Groenen JTM, Eun MY (1998) Integrated map of AFLP, SSLP and RFLP markers using a recombinant inbred population of rice (Oryza sativa L.). Theor Appl Genet 97:370–380

    CAS  Google Scholar 

  • Dabul ANG, Belefant-Miller H, RoyChowdhury M, Hubstenberger JF, Lorence A, Phillips GC (2009) Screening of a broad range of rice (Oryza sativa L.) germplasm for in vitro rapid plant regeneration and development of an early prediction system. In Vitro 44:414–420

    Google Scholar 

  • Echart-Almeida C, Cavalli-Molina S (2000) Hordein variation in Brazilian barley varieties (Hordeum vulgare L.) and wild barley (H. euclaston Steud. and H. stenostachys Godr.). Genet Mol Biol 23:425–433

    CAS  Google Scholar 

  • Eizenga GC, Agrama HA, Lee FN, Yan W, Jia Y (2006) Identifying novel resistance genes in newly introduced blast resistant rice germplasm. Crop Sci 46:1870–1878

    CAS  Google Scholar 

  • Elias M, Panaud O, Robert T (2000) Assessment of genetic variability in a traditional cassava (Manihot esculenta Crantz) farming system, using AFLP markers. Heredity 85:219–230

    PubMed  CAS  Google Scholar 

  • Fujino K, Sekiguchi H, Sato T, Kiuchi H, Nonoue Y, Takeuchi Y, Ando T, Lin SY, Yano M (2004) Mapping of quantitative trait loci controlling low-temperature germinability in rice (Oryza sativa L.). Theor Appl Genet 108:794–799

    PubMed  CAS  Google Scholar 

  • Gealy DR, Mitten DH, Rutger JN (2003) Gene flow between red rice (Oryza sativa) and herbicide-resistant rice (O. sativa): implications for weed management. Weed Technol 17:627–645

    Google Scholar 

  • Hainer A, Hesemann CU (1988) Cytogenetic investigations in rye, wheat and triticale 3. C-banding of tetra- and hexaploid wheat by Giemsa- and/or Leishman staining. Theor Appl Genet 75:305–308

    Google Scholar 

  • Han LZ, Zhang YY, Qiao YL, Cao GL, Zhang SY, Kim JH, Koh HJ (2006) Genetic and QTL analysis for low-temperature vigor of germination in rice. Acta Gen Sinica 33:998–1006

    CAS  Google Scholar 

  • Hoa TTC, Al-Babili S, Schaub P, Potrykus I (2003) Golden Indica and Japonica rice lines amenable to deregulation. Plant Physiol 133:161–169

    PubMed  CAS  Google Scholar 

  • Iwata I, Fujino K (2010) Genetic effects of major QTLs controlling low-temperature germinability in different genetic backgrounds in rice (Oryza sativa L.). Genome 53:763–768

    PubMed  Google Scholar 

  • Ji SL, Jiang L, Wang YH, Zhang WW, Liu X, Liu SJ, Chen LM, Zhai HQ, Wan JM (2009) Quantitative trait loci mapping and stability for low temperature germination ability of rice. Plant Breed 128:387–392

    Google Scholar 

  • Johnston TH, Adair CR (1965) Vegold rice. Crop Sci 5:286–287

    Google Scholar 

  • Johnston TH, Webb BD, Evans KO (1968) Registration of Starbonnet rice. Crop Sci 8:400

    Google Scholar 

  • Loxdale HD (2008) The nature and reality of the aphid clone: genetic variation, adaptation and evolution. Agric Entomol 10:81–90

    Google Scholar 

  • Lu H, Redus MA, Coburn JR, Rutger JN, McCouch SR, Tai TH (2005) Population structure and breeding patterns of 145 U.S. rice cultivars based on SSR marker analysis. Crop Sci 45:66–76

    CAS  Google Scholar 

  • Miura K, Lin SY, Yano M, Nagamine T (2001) Mapping quantitative trait loci controlling low temperature germinability in rice (Oryza sativa L.). Breed Sci 51:293–299

    CAS  Google Scholar 

  • Moldenhauer KAK, Gibbons JW, Anders MM, Lee FN, Bernhardt JL, Wilson CE, Cartwright RD, Norman RJ, Blocker MM, Boyett VA, Tolbert AC, Taylor K, Bulloch JM (2007) Registration of ‘Spring’ rice. Crop Sci 47:447–449

    Google Scholar 

  • Morsy MR, Almutairi AM, Gibbons J, Yun SJ, de los Reyes BG (2005) The OsLti6 genes encoding low-molecular-weight membrane proteins are differentially expressed in rice cultivars with contrasting sensitivity to low temperature. Gene 344:171–180

    PubMed  CAS  Google Scholar 

  • Nandakumar N, Singh AK, Sharma RK, Mohapatra T, Prabhu KV, Zaman FU (2004) Molecular fingerprinting of hybrids and assessment of genetic purity of hybrid seeds in rice using microsatellite markers. Euphytica 136:257–264

    CAS  Google Scholar 

  • Olufowote JO, Xu Y, Chen X, Park WD, Beachell HM, Dilday RH, Goto M, McCouch SR (1997) Comparative evaluation of within-cultivar variation of rice (Oryza sativa L.) using microsatellite and RFLP markers. Genome 40:370–378

    PubMed  CAS  Google Scholar 

  • Smart AJ, Vogel KP, Moser LE, Stroup WW (2003) Divergent selection for seedling tiller number in big bluestem and switchgrass. Crop Sci 43:1427–1433

    Google Scholar 

  • Soleimani VD, Baum BR, Johnson DA (2002) AFLP and pedigree-based genetic diversity estimates in modern cultivars of durum wheat [Triticum turgidum L. subsp. durum (Desf.) Husn.]. Theor Appl Genet 104:350–357

    PubMed  CAS  Google Scholar 

  • Soleimani VD, Baum BR, Johnson DA (2005) Genetic diversity among barley cultivars assessed by sequence-specific amplification polymorphism. Theor Appl Genet 110:1290–1300

    PubMed  CAS  Google Scholar 

  • Steiger DL, Nagai C, Moore PH, Morden CW, Osgood RV, Ming R (2002) AFLP analysis of genetic diversity within and among Coffea arabica cultivars. Theor Appl Genet 105:209–215

    PubMed  CAS  Google Scholar 

  • Sthapit BR, Witcombe JR (1998) Inheritance of tolerance to chilling stress in rice during germination and plumule greening. Crop Sci 38:660–665

    Google Scholar 

  • Takesawa T, Ito M, Kanzaki H, Kameya N, Nakamura I (2002) Over-expression of ζ glutathione S-transferase in transgenic rice enhances germination and growth at low temperature. Mol Breed 9:93–101

    CAS  Google Scholar 

  • Tian X, Zheng J, Songnian H, Yu J (2006) The rice mitochondrial genomes and their variations. Plant Physiol 140:401–410

    PubMed  CAS  Google Scholar 

  • Wang Y, Li J (2011) Branching in rice. Curr Opin Plant Biol 14:94–99

    PubMed  CAS  Google Scholar 

  • Wen W, Mai H, Feng F, Yu S, Huang Z, Wu J, Chen L, Xu S, Luo L (2009) Population structure and association mapping on chromosome 7 using a diverse panel of Chinese germplasm of rice (Oryza sativa L.). Theor Appl Genet 119:459–470

    PubMed  Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Corresponding authors

Correspondence to Helen Belefant-Miller or Karen A. K. Moldenhauer.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Belefant-Miller, H., Miller, G.H. & Moldenhauer, K.A.K. Utilizing the genetic diversity within rice cultivars. Planta 235, 641–647 (2012). https://doi.org/10.1007/s00425-011-1566-x

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s00425-011-1566-x

Keywords

Navigation