Chromosome pairing within genomes in maize-Tripsacum hybrids.

When the ten chromosomes of maize were inserted inlto a polyploid (2n = 72) Tripsacum dactyloides background they formed up to five pairs at meiosis. Two plants that each contained 36 Tripsacum and 14 maize chromosomes were deprived from the F(1) of maize x Tripsacum. Chromo. somes of these plants frequently formed 25 bivalents, 18 between Tripsacum chromosomes and seven between maize chromosomes. Maize chromosomes could be distinguished from Tripsacum chromosomes on the basis of size. The withint-genome pairing is probably induced by the genetic background.

Tripsacum-maize interaction: a novel cytogenetic system.

The genera Zea and Tripsacum cross readily when they are not isolated by gametophytic barriers, and it has been postulated that intergeneric introgression played a role in the evolution of maize. The basic x = 9 Tripsacum and x = 10 Zea genomes have little cytological affinity for each other in hybrids that combine 10 Zea with 18 Tripsacum chromosomes. However, one to four Tripsacum chromosomes sometimes associate with Zea chromosomes in hybrids between Z. mays (2n = 20) and T. dactyloides (2n = 72). These hybrids with 10 Zea and 36 Tripsacum chromosomes frequently produce functional female gametes with 36 Tripsacum chromosomes only. When they are pollinated with maize, their offspring again have 36 Tripsacum and 10 maize chromosomes, but the Tripsacum genome is contaminated with maize genetic material. In these individuals, intergenome pairing is the rule, and when they are pollinated with maize, their offspring have 36 Tripsacum and 10, 12, 14, 16, 18, or 20 Zea chromosomes. Plants with 36 Tripsacum and 20 Zea chromosomes behave cytologically as alloploids, although the Tripsacum genome is contimated with maize, and one basic maize genome is contaminated with with Tripsacum genetic material. When they are pollinated with maize, offspring with 18 Tripsacum and 20 Zea chromosome are obtained. Further successive backcrosses with maize selectively eliminate Tripsacum chromosomes, and eventually plants with 2n = 20 Zea chromosomes are recovered. Many of these maize plants are highly "tripsacoid." Strong gametophytic selection for essentially pure Zea gametes, however, eliminates all obvious traces of Tripsacum morphology within a relatively few generations.

The role of therapeutic drug monitoring in the care of epileptic patients.

Plasma concentrations of anti-epileptic drugs were measured in outpatients with a positive diagnosis of idiopathic epilepsy. Dosage adjustments were based on pharmacokinetic principles to obtain optimal seizure control and drug utilization. By means of the sign test the decrease in the frequency of seizures was shown to be statistically significant (P = 0,00024), as was the decrease in the number of anti-epileptic drugs being used concurrently (P = 0,00098). Combined with judicious clinical observation, measurement of blood levels of antiepileptic drugs can contribute greatly to the successful management of the epileptic patient.

Analysis of recombination rate in female and male gametogenesis in pearl millet (Pennisetum glaucum) using RFLP markers.

Sex as a factor affecting recovered recombination in plant gametes was investigated in pearl millet, Pennisetum glaucum, by using reciprocal three-way crosses [(AxB)xCvCx(A x B)]. The two populations were mapped at 42 loci pre-selected to cover the majority of the genome. No differences in recombination distances were observed at the whole-genome level and only a few individual linkage intervals were found to differ, all in favour of increased recombination through the male. Distorted segregations found in the three-way crosses provide evidence of post-gametic selection for particular gene(s) or chromosome regions. The significance of these results for the design of pearl millet breeding programmes and inheritance experiments, as well as for other experimental strategies, is discussed.