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Dive into the research topics where Sylvie Corneille is active.

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Featured researches published by Sylvie Corneille.


Molecular Genetics and Genomics | 2000

Conservation of RNA editing between rice and maize plastids: are most editing events dispensable?

Sylvie Corneille; Kerry Lutz; Pal Maliga

Abstract. The extent of conservation of RNA editing sites in the plastid genome of rice was determined by comparing the genomic sequence with that of the cDNA. The presence of a T in the cDNA predicted to be a C by the DNA sequence of the plastid genome, indicated C to U editing. In the 11 plastid transcripts of rice a total of 21 editing sites were found. In maize, a closely related grass species, 26 editing sites have been reported in 13 plastid transcripts. Most editing sites are conserved between the two species, although differences in RNA editing were found at eight sites. In seven cases the T was already encoded at the DNA level, eliminating the requirement for RNA editing. In one case (rpoB, codon 206) the RNA sequence was conserved between the two species, but the mRNA is still not edited in rice. It appears that, although evolutionarily conserved, RNA editing is essential only for a few plastid editing sites. Information about RNA editing in rice plastids will facilitate the design of plastid vectors with broad applicability in grass species.


Plant biotechnology 2002 and beyond. Proceedings of the 10th IAPTC&B Congress, Orlando, Florida, USA, 23-28 June, 2002 | 2003

Tobacco Chloroplasts as a Platform for Vaccine Production

Pal Maliga; Hiroshi Kuroda; Sylvie Corneille; Kerry Lutz; Arun K. Azhagiri; Zora Svab; John S. Tregoning; Peter Nixon; Gordon Dougan

Initial developments in the field of plant-based vaccines have been limited by low level of immunogen expression from nuclear genes. An alternative method is to express vaccine antigens from the chloroplast genome. Recently, we developed a production system for expression of recombinant proteins in tobacco chloroplasts including vectors, expression cassettes, and a system for marker gene elimination. This development is reviewed here. For general reviews on plastid transformation see (Bock, 2001; Maliga, 2002; Staub, 2002).


Plant Journal | 2001

Efficient elimination of selectable marker genes from the plastid genome by the CRE-lox site-specific recombination system.

Sylvie Corneille; Kerry Lutz; Zora Svab; Pal Maliga


Plant Journal | 2004

A novel approach to plastid transformation utilizes the phiC31 phage integrase

Kerry Lutz; Sylvie Corneille; Arun K. Azhagiri; Zora Svab; Pal Maliga


Plant Journal | 2003

Identification of functional lox sites in the plastid genome

Sylvie Corneille; Kerry Lutz; Arun K. Azhagiri; Pal Maliga


Archive | 2000

Site-specific recombination system to manipulate the plastid genome of higher plants

Pal Maliga; Sylvie Corneille; Kerry Lutz


Archive | 2002

Integrases for the insertion of heterolgogous nucleic acids into the plastid genome

Pal Maliga; Sylvie Corneille; Kerry Lutz


Science Access | 2001

Chloroplasts for the production of recombinant proteins

Pal Maliga; Hiroshi Kuroda; Sylvie Corneille


Archive | 2002

Transgenic plants having transformed plastid genomes and progeny thereof

Pal Maliga; Sylvie Corneille; Kerry Lutz


Archive | 2000

Orts-spezifisches rekombinationssystem zur manipulation des plastidengenoms in höheren pflanzen Plant location-specific recombination to manipulation of the plastid genome in higher

Sylvie Corneille; Kerry Jackson Lutz; Pal East Brunswick Maliga

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Gordon Dougan

Wellcome Trust Sanger Institute

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