Jsc. Smith et Jc. Register, GENETIC PURITY AND TESTING TECHNOLOGIES FOR SEED QUALITY - A COMPANY PERSPECTIVE, Seed science research, 8(2), 1998, pp. 285-293
A high level of genetic purity in crop varieties must be achieved and
maintained for agronomic performance as well as to encourage investmen
t and innovation in plant breeding and to ensure that the improvements
in productivity and quality imparted by breeders are delivered to the
farmer and, ultimately, to the consumer. Traditionally, morphological
comparisons have formed the basis for genetic purity evaluations. How
ever, replicated field observations are time-consuming, expensive and
unreliable. Morphology cannot provide information on the purity of spe
cific genetic attributes that relate to grain quality or to pest or he
rbicide resistance bred into varieties. Biochemical assays, including
isozymes, can distinguish varieties within several species. Isozymes h
ave been routinely used in checking seed-lot purity in maize (Zea mays
L.) for the past 20 years. Newer DNA-based technologies such as restr
iction fragment length polymorphisms and more recently developed metho
ds that use the polymerase chain reaction can allow even more discrimi
native and faster identification of varieties. However, none of the DN
A methods have replaced biochemical methods for seed purity assays, ot
her than in a relatively select group of crops with very high seed val
ue, due to their high datapoint cost. It will require further miniatur
ization, automation and enhanced capabilities to process numerous samp
les simultaneously before newly developed methods supplant biochemical
methods for routine usage in purity testing. New varieties that have
major genes for herbicide or insect resistance incorporated within the
m require purity assays during product development and following seed
production of the commercial variety. Immunological or DNA sequence as
says can be developed and automated systems are required to process hu
ndreds of thousands of individuals. Ultra-high, micro-array technologi
es and single-molecule detection systems are now under development. Th
ese technologies offer the promise that adequate distinction and high
sample throughput will be combined. New methods may eclipse the capabi
lities of biochemical methodologies, thereby potentially raising genet
ic purity standards and enabling farmers and consumers better to utili
ze and benefit from increasingly productive Varieties that are bred fr
om a more diverse base of genetic resources.