Nitrous oxide (N2O) is effective in chromosome doubling
of maize seedlings
Chromosome doubling of maize is important for subsequent haploid breeding and production of polyploid series. Recently successful chromosome doubling of maize calli has been reported using colchicine or other antimicrotubule herbicides in maize anther culture, though chromosome doubling of maize seedlings still remains difficult. The problems to address in the seedling treatment include the permeability of the leaf tissues of maize to the colchicine solution and/or prolonged effect of colchicine on maize growing tissues. The author proposes here the use of a gaseous substance, nitrous oxide (N2O), for chromosome doubling of maize seedlings.
A diploid inbred line Oh43 (2n=20) was used in this experiment. Ten seedlings with a shoot length of 2 cm were treated with a gaseous mixture (1 atm air and 8 atm N2O) for one to four days in an iron container (15 cm diameter, 20 cm height) at 28 C. The shoot meristem tissues of the treated seedlings were cut and fixed in an ethanol acetic acid solution (3:1) just after the treatments, and the effect of nitrous oxide on cell mitosis and ploidy was examined microscopically for each of four preparations.
N2O gas affected significantly the mitosis of maize cells. Normal anaphase cells were completely replaced by N2O-anaphase cells (Figure 1, Table 1). There was a reduction in the proportion of prophase cells and an increase in the number of metaphase cells. In the three- and four-day treatment, mitotic indexes decreased. Tetraploid cells were observed in all the treatments (1-4 days) (Figure 2, Table 2). In the four-day treatment, thirty-five percent of dividing cells were tetraploid and one octoploid cell was observed.
The seedlings subjected to the four-day treatment recovered from N2O injury within two weeks. The ploidy level of three root tips and one shoot meristem of one of the seedlings (four-day treatment) was analyzed. The shoot and one root tip were diploid and one of the remaining two root tips was tetraploid, while the third root tip showed a mixture of diploid and octoploid cells. Further analysis on the remaining seedlings is currently underway.
Table 1. Mitotic index and incidence of cells in prophase, metaphase
and anaphase in the N2O-treated maize shoot meristem.
|Days of treatment||Mitotic index (%)||Prophase (%)||Metaphase (%)||Anaphase (%)||N2O-anaphase (%)||No. of dividing cells observed|
Table 2. Incidence of diploid, tetraploid and octoploid cells in N2O-treated
maize shoot meristem.
|Days of treatment||Diploid cells (%)||Tetraploid cells (%)||Octoploid cells (%)||No. of dividing cells observed|
Figure 1. Anaphase of normal mitosis (left) and N2O-induced abnormal anaphase (right).
Figure 2. N2O-induced tetraploid cell (left) and octoploid cell (right).
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