Principles of Plant Genetics and Breeding. George Acquaah

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style="font-size:15px;">      The breeder influences the outcome of a mating by the choice of parents, the control over the frequency each parent is involved in mating, and the number of offspring per mating, among other ways. A mating may be as simple as a cross between two parents, to the more complex diallele mating.

       Hybrid crosses

      These are reviewed here to give the student a basis for comparison with the random mating schemes to be presented.

       Single cross = A × B → F1 (AB)

       3‐way cross = (A × B) → F1 × C → (ABC)

       Backcross = (A × B) → F1 × A → (BC1)

       Double cross = (A × B) → FAB; (C × D) → FCD; FAB × FCD → (ABCD)

      These crosses are relatively easy to genetically analyze. The breeder exercises significant control over the mating structure.

       Mating designs for random mating populations

      The term mating design is usually applied to schemes used by breeders and geneticists to impose random mating for a specific purpose. To use these designs, certain assumptions are made by the breeder:

       The materials in the population have diploid behavior. However, polyploids that can exhibit disomic inheritance (alloploids) can be studied.

       The genes controlling the trait of interest are independently distributed among the parents (i.e. uncorrelated gene distribution).

       Absence of: non‐allelic interactions, reciprocal differences, multiple alleles at the loci controlling the trait, and GxE interactions.

       Biparental mating (or pair crosses)

      In this design, the breeder selects a large number of plants (n) at random and crosses them in pairs to produce ½ n full‐sib families. The biparental (BIP) is the simplest of the mating designs. If r plants per progeny family are evaluated, the variation within and between families may be analyzed as follows:

Source df MS EMS
Between families (½ n) − 1 MS1 σ2w + rσ2b
Within families ½ n(r − 1) MS2 σ2w

      where σ2b is the covariance of full‐sibs (= ½ VA + ¼ VD + VEC = 1/r (MS1 − MS2) and σ2w = ½ VA + ¾ VD + VEW = MS2)

      The limitation of this otherwise simple to implement design is its inability to provide the needed information to estimate all the parameters required by the model. The progeny from the design comprise full‐sibs or unrelated individuals. There is no further relatedness among individuals in the progeny. The breeder must make unjustifiable assumptions in order to estimate the genetic and environmental variance.

       Polycross

      This design is for intermating a group of cultivars by natural crossing in an isolated block. It is most suited to species that are obligate cross‐pollinated (e.g. forage grasses and legumes, sugarcane, sweet potato), but especially those that can be vegetatively propagated. It provides an equal opportunity for each entry to be crossed with every other entry. It is critical that the entries be equally represented and randomly arranged in the crossing block. If 10 or less genotypes are involved, the Latin square design may be used. For a large number of entries, the completely randomized block design may be used. In both cases, about 20–30 replications are included in the crossing block. The ideal requirements are hard to meet in practice because of several problems, placing the system in jeopardy of deviating from random mating. If all the entries do not flower together, mating will not be random. To avoid this, the breeder may plant late flowering entries earlier.

      Pollen may not be dispersed randomly, resulting in concentrations of common pollen in the crossing block. Half‐sibs are generated in a polycross because progeny from each entry has a common parent. The design is used in breeding to produce synthetic cultivars, recombining selected entries of families in recurrent selection breeding programs, or for evaluating the GCA of entries.

       North carolina design I

Schematic illustration of the North Carolina Design I. (a) This design is a nested arrangement of genotypes for crossing in which no male is involved in more than one cross. (b) A practical layout in the field.

      The total variance is partitioned as follows:

Source df MS EMS
Males n−1 MS1 σ2w + rσ2flm + rfσ2m
Females n1(n2 – 1) MS2 σ2w + rσ2flm
Within progenies n1n2(r − 1) MS3 σ2w
equation equation

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