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Physiological, biochemical, and molecular characterization of a new female sterile mutant in turnip

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Abstract

A female sterile plant with aborted pistils was previously obtained in an advanced self-pollinated turnip inbred line. Cross progeny with normal wild-type (WT) plants successfully characterized the mechanism of pistil abortion, and the mutant was designated ‘tpa’ (turnip pistil abortion). Further morphological investigations showed that the tpa mutant included two phenotypes, pistil abortion partially (PAP) and pistil abortion completely (PAC), and our recent result showed that the tpa trait was controlled by two recessive genes (Wu et al. 2011). In this study, comparisons of the floral organs indicated that corolla size and petal, sepal, filament, and anther length measurements did not significantly differ between the tpa and WT plants. Subsequently, the activities of enzymes (catalase, ascorbate peroxidase, and guaiacol peroxidase) related to the metabolism of reactive oxygen, the O 2 production rate, as well as the contents of hydrogen peroxide and malondialdehyde were tested and found to be generally higher in tpa floral organs than in the WT. The reverse was true for the flower stems, however. Quantitative differences in peroxidase, cytochrome oxidase, and esterase isoenzyme patterns were also detected among these different organs. These findings suggest that pistil abortion is probably correlated with the unbalanced homeostasis of ROS antioxidant enzymes. Moreover, a specific band was recognized exclusively in the tpa plants using random amplified polymorphic DNA analysis. Sequencing and blasting results indicated that the 878-bp DNA fragment was located in the D1/D2/D3 region, near the 5′ end of the 26S rDNA. This study valuably adds to the current knowledge of and will help further elucidate the biological mechanism of female sterility induction.

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Abbreviations

APX:

Ascorbate peroxidase

CAT:

Catalase

COD:

Cytochrome oxidase

EDTA:

Ethylenediaminetetraacetic acid

EST:

Esterase

GPX:

Guaiacol peroxidase

H2O2 :

Hydrogen peroxide

MDA:

Malondialdehyde

O 2 :

Superoxide anion radical

PAC:

Pistil aborted completely

PAGE:

Polyacrylamide gel electrophoresis

PAP:

Pistil aborted partially

POD:

Peroxidase

RAPD:

Random amplified polymorphic DNA

rDNA:

Ribosomal DNA

ROS:

Reactive oxygen species

TBA:

2-thiobarbituric acid

References

  • Abbasi B, Khan M, Guo B, Bokhari SA, Khan MA (2011) Efficient regeneration and antioxidative enzyme activities in Brassica rapa var. turnip. Plant Cell Tissue Organ Cult 105:337–344

    Article  CAS  Google Scholar 

  • Arthur L, Ozias-Akins P, Hanna WW (1993) Female sterile mutant in pearl millet: evidence for initiation of apospory. J Hered 84(2):112–115

    Google Scholar 

  • Bingham ET, Hawkins-Pfeiffer J (1984) Female sterility in alfalfa due to a recessive trait retarding integument development. J Hered 75(3):231

    Google Scholar 

  • Bradford MM (1976) A rapid and sensitive method for the quantitation of microgram quantities of protein utilizing the principle of protein-dye binding. Anal Biochem 72(1–2):248–254

    Article  PubMed  CAS  Google Scholar 

  • Brewbaker JL, Upadhya MD, Mäkinen Y, Macdonald T (1968) Isoenzyme polymorphism in flowering plants III gel electrophoretic methods and applications. Physiol Plant 21(5):930–940

    Article  CAS  Google Scholar 

  • Brewer GJ (1970) An introduction to isoenzyme techniques. Academic Press, New York

    Google Scholar 

  • Cakmak I, Marschner H (1992) Magnesium deficiency and high light intensity enhance activities of superoxide dismutase, ascorbate peroxidase, and glutathione reductase in bean leaves. Plant Physiol 98(4):1222–1227

    Article  PubMed  CAS  Google Scholar 

  • Casady A, Heyne E, Weibel DE (1960) Inheritance of female sterility in sorghum. J Hered 51(1):35–38

    Google Scholar 

  • Chantha SC, Gray-Mitsumune M, Houde J, Matton DP (2010) The MIDASIN and NOTCHLESS genes are essential for female gametophyte development in Arabidopsis thaliana. Physiol Mol Biol Plants 16(1):3–18

    Article  CAS  Google Scholar 

  • Chen XJ, Qi CK, Zhang JF, Pu HM, Gao JQ, Fu SZ (2003) A primary study on biological characteristics of female sterile mutant FS-Ml of rapeseed (Brassica napus L.). Chin J Oil Crop Sci 25(3):12–15 (in Chinese with English Abstract)

    Google Scholar 

  • Coen ES, Meyerowitz EM (1991) The war of the whorls: genetic interactions controlling flower development. Nature 353(6339):31–37

    Article  PubMed  CAS  Google Scholar 

  • Daskalov S, Mihailov L (1988) A new method for hybrid seed production based on cytoplasmic male sterility combined with a lethal gene and a female sterile pollenizer in Capsicum annuum L. Theor Appl Genet 76(4):530–532

    Article  Google Scholar 

  • Dhesi JS (1966) An embryological study of female sterility in cotton. J Hered 57(6):247–248

    Google Scholar 

  • Dhindsa RS, Pulmb-Dhindsa P, Thorpe TA (1981) Leaf senescence: correlated with increased levels of membrane permeability and lipid peroxidation and decreased levels of superoxide dismutase and catalase. J Exp Bot 32:93–101

    Article  CAS  Google Scholar 

  • Dou BD, Zhang XL, Ma L, Feng DJ, Sun QX (2001) A preliminary study on female sterility in wheat. Acta Agron Sinica 27(6):1013–1016 (in Chinese)

    Google Scholar 

  • Elstner EF, Heupel A (1975) Inhibition of nitrite formation from hydroxylammoniumchloride: a simple assay for superoxide dismutase. Anal Biochem 70:616–620

    Article  Google Scholar 

  • Ficcadenti N, Sestili D, Pandolfini T, Cirillo C, Rotino GL, Spena A (1999) Genetic engineering of parthenocarpic fruit development in tomato. Mol Breeding 5(5):463–470

    Article  Google Scholar 

  • Goldman M, Goldberg R, Mariani C (1994) Female sterile tobacco plants are produced by stigma-specific cell ablation. EMBO J 13(13):2976–2984

    PubMed  CAS  Google Scholar 

  • Hanson M, Bentolila S (2004) Interactions of mitochondrial and nuclear gene that affect male gametophyte development. Plant Cell 16(Suppl.):S154–S169

    PubMed  CAS  Google Scholar 

  • Honma C, Phatak SC (1964) A female-sterile mutant in the tomato. J Hered 55(3):143–145

    Google Scholar 

  • Huang B, Sheridan W (1996) Embryo sac development in the maize indeterminate gametophyte1 mutant: abnormal nuclear behavior and defective microtubule organization. Plant Cell 8:1391–1407

    PubMed  CAS  Google Scholar 

  • Huang R, Xia R, Hu L, Lu Y, Wang W (2007) Antioxidant activity and oxygen-scavenging system in orange pulp during fruit ripening and maturation. Sci Hortic 113(2):166–172

    Article  CAS  Google Scholar 

  • Kartal G, Temel A, Arican E, Gozukirmizi N (2009) Effects of brassinosteroids on barley root growth, antioxidant system and cell division. Plant Growth Regul 58:261–267

    Article  CAS  Google Scholar 

  • Lee BR, Li LS, Jung WJ, Jin YL, Avice JC, Ourry A, Kim TH (2009) Water deficit-induced oxidative stress and the activation of antioxidant enzymes in white clover leaves. Biol Plant 53(3):505–510

    Article  Google Scholar 

  • Li FL, Shen XH, Li Y (1992) Discovery and analysis of female infertility of clone No. 28 in seed orchard of Pinus tabulaeformis Carr. J Hebei For College 7(2):93–98 (in Chinese with English Abstract)

    Google Scholar 

  • Li SC, Yang L, Deng QM, Wang SQ, Wu FQ, Li P (2006) Phenotypic characterization of a female sterile mutant in rice. J Integr Plant Biol 48(3):307–314

    Article  Google Scholar 

  • Liu YS, Zhou KD, Yin GD, Luo WZ (1993) Preliminary cytological observations on female sterility of hybrids between indica and japonica rice. Acta Biol Exp Sin 26:95–99 (in Chinese with English Abstract)

    Google Scholar 

  • Mittler R (2002) Oxidative stress, antioxidants and stress tolerance. Trends Plant Sci 7(9):405–410

    Article  PubMed  CAS  Google Scholar 

  • Mýtinová Z, Motyka V, Haisel D, Lubovská Z, Trávníčková A, Dobrev P, Holík J, Wilhelmová N (2011) Antioxidant enzymatic protection during tobacco leaf ageing is affected by cytokinin depletion. Plant Growth Regul 65:23–34

    Article  Google Scholar 

  • Nakano Y, Asada K (1981) Hydrogen peroxide is scavenged by ascorbate-specific peroxidase in spinach chloroplasts. Plant Cell Physiol 22(5):867

    CAS  Google Scholar 

  • Oka HI (1957) Genic analysis for the sterility of hybrids between distantly related varieties of cultivated rice. J Genet 55(3):397–409

    Article  Google Scholar 

  • Pannell JR (2002) The evolution and maintenance of androdioecy. Annu Rev Ecol Syst 33:397–425

    Article  Google Scholar 

  • Parida AK, Das AB, Mohanty P (2004) Defense potentials to NaCl in a mangrove, Bruguiera parviflora: differential changes of isoforms of some antioxidative enzymes. J Plant Physiol 161(5):531–542

    Article  PubMed  CAS  Google Scholar 

  • Patterson BD, MacRae EA, Ferguson IB (1984) Estimation of hydrogen peroxide in plant extracts using titanium (IV). Anal Biochem 139:487–492

    Article  PubMed  CAS  Google Scholar 

  • Pereira TNS, Lersten NR, Palmer RG (1997) Genetic and cytological analyses of a partial-female-sterile mutant (PS-1) in soybean (Glycine max; Leguminosae). Am J Bot 84(6):781–791

    Article  PubMed  CAS  Google Scholar 

  • Robinson-Beers K, Pruitt RE, Gasser CS (1992) Ovule development in wild-type Arabidopsis and two female-sterile mutants. Plant Cell 4(10):1237–1249

    PubMed  Google Scholar 

  • Shi DQ, Liu J, Xiang YH, Ye D, Sundaresan V, Yang WC (2005) SLOW WALKER1, essential for gametogenesis in Arabidopsis, encodes a WD40 protein involved in 18S ribosomal RNA biogenesis. Plant Cell 17(8):2340–2354

    Article  PubMed  CAS  Google Scholar 

  • Sood S, Vyas D, Nagar PK (2006) Physiological and biochemical studies during flower development in two rose species. Sci Hortic 108(4):390–396

    Article  CAS  Google Scholar 

  • Theißen G (2001) Development of floral organ identity: stories from the MADS house. Curr Opin Plant Biol 4(1):75–85

    Article  PubMed  Google Scholar 

  • Tiwari BS, Belengh B, Levine A (2002) Oxidative stress increased respiration and generation of reactive oxygen species, resulting in ATP depletion, opening of mitochondrial permeability transition, and programmed cell death. Plant Physiol 128:1271–1281

    Article  PubMed  CAS  Google Scholar 

  • Wan CX, Li SQ, Wen L, Kong J, Wang Q, Zhu YG (2007) Damage of oxidative stress on mitochondria during microspores development in Honglian CMS line of rice. Plant Cell Rep 26(3):373–382

    Article  PubMed  CAS  Google Scholar 

  • Winiarczyk K, Kosmala A (2009) Development of the female gametophyte in the sterile ecotype of the bolting Allium sativum L. Sci Hortic 121:353–360

    Article  Google Scholar 

  • Wu T, Cao JS (2008) Comparison of protein profile and peroxidases in bush and vine-type tropical pumpkin. J Am Soc Hort Sci 133(3):315–319

    Google Scholar 

  • Wu T, Cao JS, Zhang YF (2008) Comparison of antioxidant activities and endogenous hormone levels between bush and vine-type tropical pumpkin (Cucurbita moschata Duchesne). Sci Hortic 116(1):27–33

    Article  CAS  Google Scholar 

  • Wu JF, Zhang HJ, Lu HY, Wang FZ, Yu XL (2011) Analysis of transcriptome differences between tpa and its wild type flowers based on the microarray in turnip. Sci Agric Sinica 44(5):972–981 (in Chinese with English Abstract)

    CAS  Google Scholar 

  • Yu XL, Cao JS, Ye WZ, Wang YQ (2004) Construction of antisense gene CYP86MF plasmid vector and obtaining male sterile transformant by pollen-tube-mediating method. J Hortic Sci Biotechnol 79(5):833–839

    CAS  Google Scholar 

  • Yuan JY, Hou XL, Zhang CW, Ye F (2007) Active oxygen metabolism in the floral buds and leaves of the new cytoplasm male sterile (CMS) line and its maintainer line of non-heading Chinese cabbage. Front Agric China 1(1):47–51

    Article  Google Scholar 

  • Zhou RY (1996) The discovery of female sterile individuals in ramie (Boehmeria nivea (L.) Gaud.). Sci Agric Sinica 29(5):96 (in Chinese with English Abstract)

    Google Scholar 

  • Zhu XH, Cao XZ, Zhu QS (1996) Cytological studies on spikelet sterility of indica-japonica hybrids in rice. Chin J Rice Sci 10(2):71–78 (in Chinese with English Abstract)

    Google Scholar 

Download references

Acknowledgments

This work was supported by the Nature Science Foundation of China (Grant 30771377), the Nature Science Foundation of Zhejiang Province (Grant Y3090294), and the Sci-Tech Project of Zhejiang Province (Grant 2009C32029).

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Correspondence to Xiaolin Yu.

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Liu, Z., Yu, X., Wang, F. et al. Physiological, biochemical, and molecular characterization of a new female sterile mutant in turnip. Plant Growth Regul 68, 239–248 (2012). https://doi.org/10.1007/s10725-012-9712-4

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  • DOI: https://doi.org/10.1007/s10725-012-9712-4

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