Welcome to Acta Agronomica Sinica,

Acta Agron Sin ›› 2012, Vol. 38 ›› Issue (05): 814-819.doi: 10.3724/SP.J.1006.2012.00814

• CROP GENETICS & BREEDING·GERMPLASM RESOURCES·MOLECULAR GENETICS • Previous Articles     Next Articles

Effect of Successive Backcrossing on Eliminating Somaclonal Variation Caused by Agrobacterium-Mediated Transformation in Rice

YANG Zhou1,2,CHEN Hao1,TANG Wei3,LIN Yong-Jun1,*   

  1. 1 National Key Laboratory of Crop Genetic Improvement / National Centre of Plant Gene Research, Huazhong Agricultural University, Wuhan
    430070, China; 2 Rice Research Institute, Jiangxi Academy of Agricultural Sciences, Nanchang 330200, China; 3 Biochemistry Department, Hubei
    University of Medicine, Shiyan 442000, China
  • Received:2011-08-29 Revised:2012-01-19 Online:2012-05-12 Published:2012-03-05
  • Contact: 林拥军, E-mail: yongjunlin@mail.hzau.edu.cn

Abstract: Somaclonal variation caused by Agrobacterium-mediated transformation influences some agronomic traits of transgenic plants. As a result, a large number of T0 regenerated plants are required in the development of transgenic crop. Here, we successively backcrossed transgenic rice (Oryza sativa L.) to progenitor variety and evaluated agronomic performance of progeny, with the objective of eliminating somaclonal variation and recovering agronomic traits of transgenic parent. Three transgenic lines possessing different insect-resistance genes from Bacillus thuringiensis (Bt) were used as donor parents. They were backcrossed successively to the progenitor variety, and the individuals of each BCnF1 generation were then selfed twice, with selection for insect-resistance. BCnF3 homozygous lines, which were selected by a germination assay, caused an insect mortality of 100% in laboratory bioassay. In the field evaluation, these lines showed obviously higher yield than the donor parents and no significant differences from the progenitor variety in most agronomic traits. These results indicate that successive backcrossing can to a large extent recover agronomic traits of transgenic rice and reduce the workload required in transgenic breeding program.

Key words: Successive backcross, Somaclonal variation, Agrobacterium-mediated transformation, Transgenic rice, Insect-resistance, Agronomic trait

[1]Hiei Y, Komari T, Kubo T. Transformation of rice mediated by Agrobacterium tumefaciens. Plant Mol Biol, 1997, 35: 205–218

[2]Lin Y J, Zhang Q F. Optimising the tissue culture conditions for high efficiency transformation of indica rice. Plant Cell Rep, 2005, 23: 540–547

[3]Shu Q Y, Cui H R, Ye G Y, Wu D X, Xia Y W, Gao M W, Altosaar I. Agronomic and morphological characterization of Agrobacterium-transformed Bt rice plants. Euphytica, 2002, 127: 345–352

[4]Dale P J, McPartlan H C. Field performance of transgenic potato plants compared with controls regenerated from tuber discs and shoot cuttings. Theor Appl Genet, 1992, 84: 585–591

[5]Wang G J, Castiglione S, Chen Y, Li L, Han Y F, Tian Y C, Gabriel D W, Han Y N, Mang K Q, Sala F. Poplar (Populus nigra L.) plants transformed with a Bacillus thuringiensis toxin gene: insecticidal activity and genomic analysis. Transgenic Res, 1996, 5: 289–301

[6]Feldmann K A, Marks M D, Christianson M L, Quatrano R S. A dwarf mutant of Arabidopsis generated by T-DNA insertion mutagenesis. Science, 1989, 243: 1351-1354

[7]Bregitzer P, Halbert S E, Lemaux P G. Somaclonal variation in the progeny of transgenic barley. Theor Appl Genet, 1998, 96: 421–425

[8]Arencibia A D, Carmona E R, Cornide M T, Castiglione S, O’Relly J, Chinea A, Oramas P, Sala F. Somaclonal variation in insect-resistant transgenic sugarcane (Saccharum hybrid) plants produced by cell electroporation. Transgenic Res, 1999, 8: 349–360

[9]Hiei Y, Ohta S, Komari T, Kumashiro T. Efficient transformation of rice (Oryza sativa L.) mediated by Agrobacterium and sequence analysis of the boundaries of the T-DNA. Plant J, 1994, 6: 271–282

[10]Labra M, Savini C, Bracale M, Pelucchi N, Colombo L, Bardini M, Sala F. Genomic changes in transgenic rice (Oryza sativa L.) plants produced by infecting calli with Agrobacterium tumefaciens. Plant Cell Rep, 2001, 20: 325–330

[11]Larkin P J, Scowcroft W R. Somaclonal variation—a novel source of variability from cell cultures for plant improvement. Theor Appl Genet, 1981, 60: 197–214

[12]Bertin P, Bouharmont J. Use of somaclonal variation and in vitro selection for chilling tolerance improvement in rice. Euphytica, 1997, 96: 135–142

[13]Van Sint Jan V, de Macedo C C, Kinet J M, Bouharmont J. Selection of Al-resistant plants from a sensitive rice cultivar, using somaclonal variation, in vitro and hydroponic cultures. Euphytica, 1997, 97: 303–310

[14]Sundaram R M, Vishnupriya M R, Biradar S K, Laha G S, Reddy G N, Rani N S, Sarma N P, Sonti R V. Marker assisted introgression of bacterial blight resistance in Samba Mahsuri, an elite indica rice variety. Euphytica, 2008, 160: 411–422

[15]Sundaram R M, Vishnupriya M R, Laha G S, Rani N S, Rao P S, Balachandran S M, Reddy G N, Sarma N P, Sonti R V. Introduction of bacterial blight resistance into Triguna, a high yielding, mid-early duration rice variety. Biotechnol J, 2009, 4: 400–407

[16]Ragagnin V A, de Souza T L P O, Sanglard D A, Arruda K M A, Costa M R, Alzate-Marin A L, Carneiro J E, Moreira M A, de Barros E G. Development and agronomic performance of common bean lines simultaneously resistant to anthracnose, angular leaf spot and rust. Plant Breed, 2009, 128: 156–163

[17]Micallef M C, Austin S, Bingham E T. Improvement of transgenic alfalfa by backcrossing. In Vitro Cell Dev Biol Plant, 1995, 31: 187–192

[18]Bregitzer P, Dahleen L S, Neate S, Schwarz P, Manoharan M. A single backcross effectively eliminates agronomic and quality alterations caused by somaclonal variation in transgenic barley. Crop Sci, 2008, 48: 471–479

[19]Chen H, Tang W, Xu C G, Li X H, Lin Y J, Zhang Q F. Transgenic indica rice plants harboring a synthetic cry2A* gene of Bacillus thuringiensis exhibit enhanced resistance against lepidopteran rice pests. Theor Appl Genet, 2005, 111: 1330–1337

[20]Tang W, Chen H, Xu C G, Li X H, Lin Y J, Zhang Q F. Development of insect-resistant transgenic indica rice with a synthetic cry1C* gene. Mol Breed, 2006, 18: 1–10

[21]Chen H, Zhang G A, Zhang Q F, Lin Y J. Effect of transgenic Bacillus thuringiensis rice lines on mortality and feeding behavior of rice stem borers (Lepidoptera: Crambidae). J Econ Entomol, 2008, 101: 182–189

[22]Murashige T, Skoog F. A revised medium for rapid growth and bioassays with tobacco tissue cultures. Physiol Plant, 1962, 15: 473–497

[23]Thompson C J, Movva N R, Tizard R, Crameri R, Davies J E, Lauwereys M, Botterman J. Characterization of the herbicide-resistance gene bar from Streptomyces hygroscopicus. EMBO J, 1987, 6: 2519–2523

[24]Kaeppler S M, Kaeppler H F, Rhee Y. Epigenetic aspects of somaclonal variation in plants. Plant Mol Biol, 2000, 43: 179–188

[25]Bergelson J, Purrington C B, Palm C J, López-Gutiérrez J C. Costs of resistance: a test using transgenic Arabidopsis thaliana. Proc Biol Sci, 1996, 263: 1659–1663

[26]Saxena D, Stotzky G. Bt corn has a higher lignin content than non-Bt corn. Am J Bot, 2001, 88: 1704–1706

[27]Zhang M(张敏), Wang X-C(王校常), Yan W-D(严蔚东), Liang Y-C(梁永超), Shi W-M(施卫明). K+ and Na+ uptake and transport and SOD activity in Bt transgenic cotton seedlings under salt stress. Acta Pedol Sin (土壤学报), 2005, 42(3): 460–467 (in Chinese with English abstract)

[28]Bates S L, Zhao J Z, Roush R T, Shelton A M. Insect resistance management in GM crops: past, present and future. Nat Biotechnol, 2005, 23: 57–62

[29]Ye R J, Huang H Q, Yang Z, Chen T Y, Liu L, Li X H, Chen H, Lin Y J. Development of insect-resistant transgenic rice with Cry1C*-free endosperm. Pest Manag Sci, 2009, 65: 1015–1020

[30]Peng J Y, Kononowicz H, Hodges T K. Transgenic indica rice plants. Theor Appl Genet, 1992, 83: 855–863
[1] ZHAO Jing, MENG Fan-Gang, YU De-Bin, QIU Qiang, ZHANG Ming-Hao, RAO De-Min, CONG Bo-Tao, ZHANG Wei, YAN Xiao-Yan. Response of agronomic traits and P/Fe utilization efficiency to P application with different P efficiency in soybean [J]. Acta Agronomica Sinica, 2021, 47(9): 1824-1833.
[2] Li-Lan ZHANG, Lie-Mei ZHANG, Huan-Ying NIU, Yi XU, Yu LI, Jian-Min QI, Ai-Fen TAO, Ping-Ping FANG, Li-Wu ZHANG. Correlation between SSR markers and fiber yield related traits in jute (Corchorus spp.) [J]. Acta Agronomica Sinica, 2020, 46(12): 1905-1913.
[3] MA Shuo, JIAO Yue, YANG Jiang-Tao, WANG Xu-Jing, WANG Zhi-Xing. Molecular characterization identification by genome sequencing of transgenic glyphosate-tolerant rice G2-7 [J]. Acta Agronomica Sinica, 2020, 46(11): 1703-1710.
[4] JIA Xiao-Ping,QUAN Jian-Zhang,WANG Yong-Fang,DONG Zhi-Ping,YUAN Xi-Lei,ZHANG Bo,LI Jian-Feng. Effects of different photoperiod conditions on agronomic traits of foxtail millet [J]. Acta Agronomica Sinica, 2019, 45(7): 1119-1127.
[5] DONG Yu-Feng, WANG Xu-Jing, SONG Ya-Ya, JIN Xi, and WANG Zhi-Xing. Cultivation of herbicide tolerant transgenic rice by gene spliting technique [J]. Acta Agronomica Sinica, 2019, 45(3): 344-353.
[6] XU Yi,ZHANG Lie-Mei,GUO Yan-Chun,QI Jian-Min,ZHANG Li-Lan,FANG Ping-Ping,ZHANG Li-Wu. Core collection screening of a germplasm population in jute (Corchorus spp.) [J]. Acta Agronomica Sinica, 2019, 45(11): 1672-1681.
[7] ZHAI Jun-Peng,LI Hai-Xia,BI Hui-Hui,ZHOU Si-Yuan,LUO Xiao-Yan,CHEN Shu-Lin,CHENG Xi-Yong,XU Hai-Xia. Genome-wide association study for main agronomic traits in common wheat [J]. Acta Agronomica Sinica, 2019, 45(10): 1488-1502.
[8] Yi XU,Lie-Mei ZHANG,Jian-Min QI,Mei SU,Shu-Sheng FANG,Li-Lan ZHANG,Ping-Ping FANG,Li-Wu ZHANG. Correlation Analysis between Yield of Bast Fiber and Main Agronomic Traits in Jute (Corchorus spp.) [J]. Acta Agronomica Sinica, 2018, 44(6): 859-866.
[9] Hong JIANG,Shi SUN,Wen-Wen SONG,Cun-Xiang WU,Ting-Ting WU,Shui-Xiu HU,Tian-Fu HAN. Characterization of Growth Period Structure and Identification of E Genes of MGIII Soybean Varieties from Different Geographic Regions [J]. Acta Agronomica Sinica, 2018, 44(10): 1448-1458.
[10] Da-Wei JIAN, Yang ZHOU, Hong-Wei LIU, Li YANG, Chun-Yan MAI, Li-Qiang YU, Xin-Nian HAN, Hong-Jun ZHANG, Hong-Jie LI. Functional Markers Reveal Genetic Variations in Wheat Improved Cultivars and Landraces from Xinjiang [J]. Acta Agronomica Sinica, 2018, 44(05): 657-671.
[11] ZHENG Li-Fei,SHANG Yi-Fei,LI Xue-Jun,FENG Hao,WEI Yong-Sheng. Structural Equation Model for Analyzing Relationshipbetween Yield and Agronomic Traits in Winter Wheat [J]. Acta Agron Sin, 2017, 43(09): 1395-1400.
[12] DUAN Shao-Guang,JIN Li-Ping*,LI Guang-Cun,BIAN Chun-Song,XU Jian-Fei,HU Jun,QU Dong-Yu. Genetic Diversity Analysis of Potato varieties [J]. Acta Agron Sin, 2017, 43(05): 718-729.
[13] ZHAO Pei,TENG Li-Jie,WANG Ke,DU Li-Pu,REN Xian,SHE Mao-Yun,YE Xing-Guo. Cloning, Molecular Characterization, and Functional Analysis of Wheat TaVIP1 Genes [J]. Acta Agron Sin, 2017, 43(02): 201-209.
[14] WANG Xin,MA Ying-Xue,YANG Yang,WANG Dan-Feng,YIN Hui-Juan,WANG Hong-Gang. Identification of Dwarfing Wheat Germplasm SN224 and Analysis of QTLs for Its Agronomic Characters [J]. Acta Agron Sin, 2016, 42(08): 1134-1142.
[15] ZHOU Lu, SHEN Bei-Bei, BAI Su-Yang, LIU Xi, JIANG Ling, ZHAI Hu-Qu, WAN Jian-Min. RNA Interference of OsGABA-T1 Gene Expression Induced GABA Accumulation in Rice Grain [J]. Acta Agron Sin, 2015, 41(09): 1305-1312.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
No Suggested Reading articles found!