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Isolation and microinjection of active sperm nuclei into egg cells and central cells of isolated maize embryo sacs

Published online by Cambridge University Press:  26 September 2008

E. Matthys-Rochon*
Affiliation:
Reconnaissance Cellulaire et Amélioration des Plantes, UMR 9938 NRS-INRA-ENS, Lyon, France.
R. Mòl
Affiliation:
Reconnaissance Cellulaire et Amélioration des Plantes, UMR 9938 NRS-INRA-ENS, Lyon, France.
P. Heizmann
Affiliation:
Reconnaissance Cellulaire et Amélioration des Plantes, UMR 9938 NRS-INRA-ENS, Lyon, France.
C. Dumas
Affiliation:
Reconnaissance Cellulaire et Amélioration des Plantes, UMR 9938 NRS-INRA-ENS, Lyon, France.
*
E. Matthys-Rochon, Reconnaissance Cellulaire et Amélioration des Plantes, UMR 9938 CNRS-INRA-ENS, Ecole Normale Supérieure de Lyon, 46 Allée d′Italie, F-69364 Lyon, Cédex 07, France. Fax: (33) 72 72 86 80.

Summary

Artificial fertilisation was attempted in maize by microinjecting sperm nuclei into the egg cell or central cell of isolated embryo sacs. A protocol for isolation of nuclei from pollen grains was developed and a pure fraction of sperm nuclei was obtained after centrifugation on a Percoll gradient. The in vitro transcriptional activity of the nuclei was tested by incorporation of radioactive UTP into RNA. The level of labelled nucleotide incorporation increased and reached a maximum after between 30 and 40 min in the incubation medium. The embryo sacs were enzymatically isolated and their viability determined by observation of cytoplasmic streaming in the female cells. The embryo sacs were immobilised by embedding in low-melting-point agarose and a single male nucleus was injected with a bevelled microcapillary. The presence of the injected nucleus in the egg or central cell was demonstrated using a cytological approach. This paper presents an alternative method for studying the intimate processes of fertilisation in plants.

Type
Commentary
Copyright
Copyright © Cambridge University Press 1994

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