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Transgenic maize plants by tissue electroporation.
Author(s) -
Kathleen D’Halluin,
Els Bonne,
Martien Bossut,
Marc De Beuckeleer,
J. Leemans
Publication year - 1992
Publication title -
the plant cell
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.324
H-Index - 341
eISSN - 1532-298X
pISSN - 1040-4651
DOI - 10.1105/tpc.4.12.1495
Subject(s) - biology , electroporation , callus , transformation (genetics) , kanamycin , zygote , protoplast , genetically modified crops , agrobacterium , transgene , botany , somatic embryogenesis , gene , embryo , microbiology and biotechnology , genetics , embryogenesis
In this paper, we describe the transformation of regenerable maize tissues by electroporation. In many maize lines, immature zygotic embryos can give rise to embryogenic callus cultures from which plants can be regenerated. Immature zygotic embryos or embryogenic type I calli were wounded either enzymatically or mechanically and subsequently electroporated with a chimeric gene encoding neomycin phosphotransferase (neo). Transformed embryogenic calli were selected from electroporated tissues on kanamycin-containing media and fertile transgenic maize plants were regenerated. The neo gene was transmitted to the progeny of kanamycin-resistant transformants in a Mendelian fashion. This showed that all transformants were nonchimeric, suggesting that transformation and regeneration are a single-cell event. The maize transformation procedure presented here does not require the establishment of genotype-dependent embryogenic type II callus or cell suspension cultures and facilitates the engineering of new traits into agronomically relevant maize inbred lines.

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