The implementation of modern inducer lines in maize breeding can substantially decrease the time required to create elite inbred lines. In industrialized countries, this method has already largely replaced conventional backcross methods. However, the application of in vivo gynogenesis for inducing doubled haploids is still limited to European and US maize germplasms and has still to be adapted for exotic plant material. The reliability of three modern European inducer lines from the University of Hohenheim (Germany) was investigated for the production of haploid progenies from subtropical specialty maize. Three Chinese hybrids heterozygous for waxy maize and opaque 2 were used as maternal donor material, as maize double recessive for waxy and opaque 2 may improve the nutrition of ethnic minorities in Southeast Asia. However, many false positives were detected by flow cytometry among putative haploid seeds based on anthocyanin pigmentation because the color expression was inhibited in almost 50% of the induced seeds from this maternal plant material. Based on flow cytometry, the haploid induction rates were high with 10.2-12.3%, and the chromosome doubling rates were around 50%; therefore the principal potential of producing DH was confirmed for subtropical maize. However inducer lines for the precise and fast recognition of truly induced haploid seeds still need to be developed.

We present a strategy for establishing a transgenic doubled haploid maize line from heterozygous transgenic material by means of anther culture. Compared to conventional inbreeding, the in vitro androgenesis technique enables a faster generation of virtually fully homozygous lines. Since the androgenic response is highly genotype-dependent, we crossed transgenic, non-androgenic plants carrying a herbicide resistance marker gene ( pat, encoding for phosphinothricin acetyl transferase) with a highly androgenic genotype. The transgenic progenies were used as donor plants for anther culture. One transgenic and three non-transgenic doubled haploid lines have been established within approximately 1 yr. The homozygosity of all four doubled haploid lines was tested by analysis of simple sequence repeat (SSR) markers at 19 different loci. Polymorphisms were found between the lines but not within the lines, indicating the homozygous nature of the entire plant genome gained by anther culture. Southern blot analysis revealed that the transgenic donor plants and their doubled haploid progeny exhibited the same integration pattern of the pat gene. No segregation of the herbicide resistance trait has been observed among the progeny of the transgenic doubled haploid line.

The aim of the present study was to determine the suitability of maize gametic embryos of three ETH genotypes as a target for biolistic transformation. We studied parameters considered essential for a successful transformation, such as the frequency of secondary embryo formation, their regeneration ability and the transient transgene expression. Transformable zygotic embryos of one of the ETH genotypes were used as positive control. Our results indicate that gametic embryos can potentially be transformed by particle bombardment, since they responded positively to all the studied parameters, although with lower efficiencies than the zygotic embryos. In particular, differences were found in the rate of secondary embryogenesis and the density of transformed cells.