Skip to main content
Log in

Cytoplasmic effects of Brassica napus and B. juncea on extreme temperature stresses of B. carinata

  • Published:
Euphytica Aims and scope Submit manuscript

    We’re sorry, something doesn't seem to be working properly.

    Please try refreshing the page. If that doesn't work, please contact support so we can address the problem.

Abstract

Alloplasmic lines of Brassica carinata were developed from the interspecific crosses B. napus × B. carinata and B. juncea × B. carinata followed by repeated backcrossing to B. carinata as the recurrent male parent up to the BC7 generation. The BC7 generations with cytoplasm of B. napus and B. juncea were designated NC-7 and JC-7, respectively, and the corresponding euplasmic lines were designated CN-7 and CJ-7, respectively. Four lines (NC-7 vs. CN-7 and JC-7 vs. CJ-7) were grown in a closed vinyl greenhouse at 55 °C and outdoors during winter in two cold regions of China (−3 to −10 °C) to investigate the heat and cold tolerance of the alloplasmic and euplasmic lines. Plants with the cytoplasm of B. napus showed lower leaf chlorophyll content and little difference in heat tolerance, whereas plants with the cytoplasm of B. juncea showed higher severity of heat injury compared with that of the euplasmic lines with cytoplasm of B. carinata. Alloplasmic plants with cytoplasm of B. napus and B. juncea showed decreased cold tolerance compared with that of euplasmic lines with cytoplasm of B. carinata. The difference in cold tolerance also was observed in the lethal temperature of the alloplasmic and euplasmic plants. The results suggest that tolerance of extreme temperature stress was controlled mainly by the nucleus but also was affected by the cytoplasm. Interaction between the maternal genome and nucleus was also observed.

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

Similar content being viewed by others

References

  • Arumugam N, Mukhopadhyay A, Gupta V, Sodhi YS, Verma JK, Pental D, Pradhan AK (2002) Synthesis of somatic hybrids (RCBB) by fusing heat-tolerant Raphanus sativus (RR) and Brassica oleracea (CC) with Brassica nigra (BB). Plant Breed 121:168–170 (short communication)

    Article  Google Scholar 

  • Banga SS, Labana KS, Medhi BN (1984) Alternaria incidence in some alloplasmic lines of Indian mustard (Brassica juncea (L.) Coss.). Theor Appl Genet 67:195–196

    Article  CAS  PubMed  Google Scholar 

  • Banga SS, Deol JS, Banga SK (2003) Alloplasmic male-sterile Brassica juncea with Enarthrocarpus lyratus cytoplasm and the introgression of gene(s) for fertility restoration from cytoplasm donor species. Theor Appl Genet 106:1390–1395

    CAS  PubMed  Google Scholar 

  • Bentolila S, Alfonso AA, Hanson MR (2002) A pentatricopeptide repeat-containing gene restores fertility to cytoplasmic male-sterile plants. Proc Natl Acad Sci USA 99:10887–10892

    Article  CAS  PubMed Central  PubMed  Google Scholar 

  • Beversdorf WD, Weiss-Lerman J, Erickson LR, Souza-Machada V (1980) Transfer of cytoplasmically-inherited triazine resistance from bird’s rape to cultivated oilseed rape (Brassica campestris and B. napus). Can J Genet Cytol 22:167–172

    Article  CAS  Google Scholar 

  • Bilger HW, Schreiber U, Lange OL (1984) Determination of leaf heat resistance: comparative investigation of chlorophyll fluorescence changes and tissue necrosis methods. Oecologia 63:256–262

    Article  Google Scholar 

  • Chang CT, Uesugi R, Hondo K, Kakihara F, Kato M (2007) The effect of the cytoplasms of Brassica napus and B. juncea on some characteristics of B. carinata, including flower morphology. Euphytica 158:261–270

    Article  Google Scholar 

  • Chang C, Kakihara F, Hondo K, Kato M (2009) Alloplasmic effects of Brassica napus and B. juncea on seed characteristics of B. carinata. Euphytica 170:317–325

    Article  CAS  Google Scholar 

  • Del Río M, De-Haro A, Fernández-Martínez JM (2003) Transgressive segregation of erucic acid content in Brassica carinata A. Braun. Theor Appl Genet 107:643–651

    Article  PubMed  Google Scholar 

  • Deol JS, Shivanna KR, Prakash S, Banga SS, Robbelen G (2003) Enarthrocarpus lyratus-based cytoplasmic male sterility and fertility restorer system in Brassica rapa. Plant Breed 122:438–440

    Article  Google Scholar 

  • Hinata K, Konno N (1979) Studies on a male sterile strain having the Brassica campestris nucleus and the Diplotaxis muralis cytoplasm. I On the breeding procedure and some characteristics of the male sterile strain. Jpn J Breed 29:305–311

    Article  Google Scholar 

  • Kempken F, Pring R (1999) Plant breeding: male sterility in higher plants-fundamentals and applications. Prog Bot 60:139–166

    CAS  Google Scholar 

  • Kitao M, Lei TT, Koike T, Tobita H, Maruyama Y, Matsumoto Y, Ang LH (2000) Temperature response and photoinhibition investigated by chlorophyll fluorescence measurements for four distinct species of dipterocarp trees. Physiol Plant 109:284–290

    Article  CAS  Google Scholar 

  • Knight CA, Ackerly DD (2002) An ecological and evolutionary analysis of photosynthetic thermotolerance using the temperature-dependent increase in fluorescence. Oecologia 130:505–514

    Article  Google Scholar 

  • Liu J-H, Landgren M, Glimelius K (1996) Transfer of the Brassica tournefortii cytoplasm to B. napus for the production of cytoplasmic male sterile B. napus. Physiol Plant 96:123–129

    Article  CAS  Google Scholar 

  • Pradhan AK, Mukhopadhyay A, Pental D (1991) Identification of the putative cytoplasmic donor of a CMS system in Brassica juncea. Plant Breed 106:204–208

    Article  Google Scholar 

  • Prakash S, Ahuja I, Upreti HC, Dinesh Kumar V, Bhat SR, Kirti PB, Chopra VL (2001) Expression of male sterility in alloplasmic Brassica juncea with Erucastrum canariense cytoplasm and the development of a fertility restoration system. Plant Breed 120:479–482

    Article  Google Scholar 

  • Schreiber U, Berry JA (1977) Heat-induced changes of chlorophyll fluorescence in intact leaves correlated with damage of the photosynthetic apparatus. Planta 136:233–238

    Article  CAS  PubMed  Google Scholar 

  • Schwarz AG, Redmann RE (1989) Photosynthetic properties of C4 grass (Spartina gracilis Trin.) from northern environment. Photosynthetica 23:449–459

    Google Scholar 

  • Smillie RM, Nott R (1979) Heat injury in leaves of alpine, temperate and tropical plants. Aust J Plant Physiol 6:135–141

    Article  CAS  Google Scholar 

  • Weng JH, Ueng RG (1997) Effect of temperature on photosynthesis of Miscanthus clones collected from different elevations. Photosynthetica 34:307–311

    Article  Google Scholar 

  • Wu Y, Zhang C, Liu C, Ren S, Zhang Y (1998) Breeding technology of alloplasmic wheat. Sci China Ser C 41:449–458

    Article  CAS  Google Scholar 

  • Yamada M, Hidaka T, Fukamachi H (1996) Heat tolerance in leaves of tropical fruit crops as measured by chlorophyll fluorescence. Sci Hortic 67:39–48

    Article  CAS  Google Scholar 

Download references

Acknowledgments

We express our sincere gratitude to Prof. Dr. Masahiro Kato, Laboratory of Plant Breeding, Faculty of Agriculture, Ehime University, Japan, for providing pertinent criticism from the beginning of this research to submission of the manuscript. We also thank the Tianjin Kernel Agricultural Science & Technology Co., Ltd for support.

Author information

Authors and Affiliations

Authors

Corresponding authors

Correspondence to Deling Sun or Fumika Kakihara.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Chang, C., Sun, D., Kakihara, F. et al. Cytoplasmic effects of Brassica napus and B. juncea on extreme temperature stresses of B. carinata . Euphytica 204, 335–342 (2015). https://doi.org/10.1007/s10681-014-1337-4

Download citation

  • Received:

  • Accepted:

  • Published:

  • Issue Date:

  • DOI: https://doi.org/10.1007/s10681-014-1337-4

Keywords

Navigation