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Correction of chlorophyll deficiency in alloplasmic male sterile Brassica juncea through recombination between chloroplast genomes

Published online by Cambridge University Press:  14 April 2009

P. B. Kirti
Affiliation:
Biotechnology Centre, Indian Agricultural Research Institute, New Delhi- 110012, India
S. B. Narasimhulu
Affiliation:
Biotechnology Centre, Indian Agricultural Research Institute, New Delhi- 110012, India
T. Mohapatra
Affiliation:
Biotechnology Centre, Indian Agricultural Research Institute, New Delhi- 110012, India
S. Prakash
Affiliation:
Biotechnology Centre, Indian Agricultural Research Institute, New Delhi- 110012, India
V. L. Chopra*
Affiliation:
Biotechnology Centre, Indian Agricultural Research Institute, New Delhi- 110012, India
*
*Corresponding author.
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Brassica juncea cv. Pusa Bold carrying B. oxyrrhina cytoplasm (oxy cytoplasm) was male sterile and chlorotic under field conditions at low temperature (Prakash & Chopra, 1990). Leaf protoplasts of the chlorotic male sterile alloplasmic line (2n = 36) were fused with hypocotyl protoplasts of green male fertile, B. juncea cv. RLM-198 (2n = 36) using polyethylene glycol. Of the 1043 plants regenerated from 10 fusion experiments, 123 had ‘gigas’ features and were identified as presumptive fusion products. Among field-grown population, one plant was dark green even at low temperatures and male sterile. It possessed 72 chromosomes which formed 36 bivalents at late diakinesis of meiosis-I. This plant was back-crossed to B. juncea cv. Pusa Bold (the maintainer line) for three successive generations. One male sterile, normal green BC3 progeny plant with 2n = 36 was analyzed for organelle constitution. Probing its total DNA with the mitochondrial gene for cytochrome oxidase subunit I revealed that it possessed mitochondria of B. oxyrrhina. Southern hybridization pattern with the gene for ribulose bisphosphate carboxylase oxygenase-large subunit (rbcL) revealed that the chloroplast genome of the chlorophyll deficiencycorrected plant had characteristics of both B. juncea and B. oxyrrhina. The deficiency correction has been attributed to recombination between chloroplast genomes of the two species.

Type
Research Article
Copyright
Copyright © Cambridge University Press 1993

References

Fejes, E., Engler, D. & Maliga, P. (1990). Extensive homologous chloroplast recombination in pi 14 Nicotiana somatic hybrid. Theoretical and Applied Genetics 79, 2832.CrossRefGoogle Scholar
Gatenby, A. A., Castleton, J. A. & Saul, M. W. (1981). Expression in E. coli of maize and wheat chloroplast genes for large subunit of ribulose bisphosphate carboxylase. Nature 291, 117121.CrossRefGoogle Scholar
Issac, P. G., Jones, V. P. & Leaver, C. J. (1985). The maize cytochrome C oxidase subunit I gene: sequence, expression and rearrangement in cytoplasmic male sterile plants. EMBO Journal 54, 16171623.CrossRefGoogle Scholar
Jarl, C. I. & Bornman, C. H. (1988). Correction of chlorophyll defective male sterile winter oilseed rape (Brassica napus) through organelle exchange: phenotypic evaluation of the progeny. Hereditas 108, 97102.CrossRefGoogle Scholar
Jarl, C. J.van, M., Grinsven, M. Q. J. & Van den Mark, F. (1989). Correction of chlorophyll defective male sterile winter oilseed rape (Brassica napus) through organelle exchange: molecular analysis of the cytoplasm of parental lines and corrected progeny. Theoretical and Applied Genetics 11, 135141.CrossRefGoogle Scholar
Kemble, R. J., Yarrow, S. A., Wu, S. C. & Barsby, T. L. (1988). Absence of mitochondrial chloroplast DNA recombination from protoplasts, protoplast fusions and anther culture. Theoretical and Applied Genetics 75, 875881.Google Scholar
Kirti, P. B. & Chopra, V. L. (1990). Rapid regeneration through organogenesis and somatic embryogenesis from cultured protoplasts of mustard Brassica juncea. Plant Cell Tissue and Organ Culture 20, 6567.CrossRefGoogle Scholar
Kirti, P. B., Prakash, S. & Chopra, V. L. (1991). Interspecific hybridization between Brassica juncea and B. spinescens through protoplast fusion. Plant Cell Reports 9, 639642.CrossRefGoogle Scholar
Medgyesy, P., Fejes, E. & Maliga, P. (1985). Interspecific chloroplast recombination on a nicotiana somatic hybrid -physical mapping of chloroplast DNA of somatic hybrid plant derived from tobacco and N. plumbaginifolia. Proceedings of the National Academy of Sciences of the USA 82, 69606964.CrossRefGoogle Scholar
Menczel, L., Morgan, A., Brown, S. & Maliga, P. (1987). Fusion mediated combination of Ogura type cytoplasmic male sterility with Brassica napus plastids using Xirradiated CMS protoplasts. Plant Cell Reports 6, 98101.CrossRefGoogle ScholarPubMed
Pelletier, G., Primard, C., Vedel, F., Chetrit, P., Remy, R., Rousselle, R. & Renard, M. (1983). Intergeneric cytoplasmic hybridization in Cruciferae by protoplast fusion. Molecular and General Genetics 191, 244250.CrossRefGoogle Scholar
Prakash, S. & Chopra, V. L. (1990). Male sterility caused by cytoplasm of Brassica oxyrrhina in B. campestris and B. juncea. Theoretical and Applied Genetics 79, 285287.CrossRefGoogle Scholar
Sacristan, M. D., Gerdemann-Knorck, M. & Schieder, O. (1989). Incorporation of hygromycin resistance in Brassica nigra and its transfer to B. napus through asymmetric protoplast fusion. Theoretical and Applied Genetics 78, 194200.CrossRefGoogle Scholar
Saghai-Maroof, M. A., Soliman, K. M., Jorgensen, R. A. & Allard, R. W. (1984). Ribosomal DNA -spacer length polymorphism in barley: Mendelian inheritance. Proceedings of the National Academy of Sciences of the USA 81, 80148018.CrossRefGoogle ScholarPubMed
Sjodin, C. & Glimelius, K. (1989). Transfer of resistance against Phoma lingam to Brassica napus by asymmetric somatic hybridization combined with toxin selection. Theoretical and Applied Genetics 78, 513520.CrossRefGoogle ScholarPubMed
Thanh, N. D. & Medgyesy, P. (1989). Limited chloroplast gene transfer via recombination overcomes plastomegenome incompatibility between Nicotiana tabacum and Solarium tuberosum. Plant Molecular Biology 12, 8793.CrossRefGoogle Scholar