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Principles of Plant Genetics and Breeding

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Single cross<br />

A × B<br />

AB<br />

Proportion A = 50%<br />

B = 50%<br />

(a)<br />

Backcross<br />

1st BC<br />

2nd BC<br />

3rd BC<br />

A × B<br />

F 1 × B<br />

BC 1F 1 × B<br />

BC 2F 1 × B<br />

BC nF 1 × B<br />

<strong>of</strong> the existing desirable traits. Hence, one (or several)<br />

parent(s) serves as a donor <strong>of</strong> specific genes <strong>and</strong> is usually<br />

involved in the cross only once. Subsequent crosses<br />

entail crossing the desirable parent (recurrent parent)<br />

repeatedly to the F 1 , in order to retrieve all the desirable<br />

traits. A commonly used convergent cross is the backcross<br />

(Figure 10.1b) (see Chapter 16).<br />

Issue <strong>of</strong> reproductive isolation barriers<br />

Hybridization is <strong>of</strong>ten conducted routinely without<br />

any problems when individuals from the same species<br />

are involved, provided there are no fertility-regulating<br />

mechanisms operating. Even when such mechanisms<br />

exist, hybridization can be successfully conducted by<br />

providing appropriate pollen sources. Sometimes, plant<br />

breeders are compelled to introduce desired genes from<br />

distant relatives or other species. Crossing plants from<br />

two different species or sometimes even plants from different<br />

genuses is more challenging <strong>and</strong> has limited<br />

success. Often, the breeder needs to use additional techniques<br />

(e.g., embryo rescue) to intervene at some point<br />

SEXUAL HYBRIDIZATION AND WIDE CROSSES IN PLANT BREEDING 171<br />

Three-way cross<br />

A × B<br />

AB × C<br />

ABC<br />

Proportion A = 25%<br />

B = 25%<br />

C = 50%<br />

Proportion <strong>of</strong> B<br />

50%<br />

75%<br />

87.5%<br />

(b)<br />

Double cross Diallel cross<br />

A × B A × B<br />

A B C D<br />

AB × CD<br />

ABCD<br />

Proportion A = 25%<br />

B = 25%<br />

C = 25%<br />

D = 25%<br />

Convergent cross<br />

(1) A × B C × D E × F G × H<br />

Proportion <strong>of</strong> A<br />

50%<br />

Figure 10.1 The basic types <strong>of</strong> crosses used by plant breeders. Some crosses are divergent (a) while others are<br />

convergent (b).<br />

A<br />

B<br />

C<br />

D<br />

E<br />

AA<br />

AB<br />

AC<br />

AD<br />

AE<br />

(2) A × B A × C A × D A × E<br />

BA<br />

BB<br />

BC<br />

BD<br />

BE<br />

25%<br />

13%<br />

CA<br />

CB<br />

CC<br />

CD<br />

CE<br />

Reciprocal<br />

50% A<br />

50%<br />

50%<br />

DA<br />

DB<br />

DC<br />

DD<br />

DE<br />

in the process in order to obtain a mature hybrid plant.<br />

This kind <strong>of</strong> crossing involving parents from different<br />

species is called a wide cross <strong>and</strong> is described further<br />

below.<br />

Reproductive isolation barriers may be classified into<br />

three categories as suggested by researchers such as G.<br />

L. Stebbins, T. Dobzhansky, <strong>and</strong> D. Zohary (Table 10.2).<br />

E<br />

EA<br />

EB<br />

EC<br />

ED<br />

EE<br />

Selfs<br />

Table 10.2 A summary <strong>of</strong> the reproductive isolation<br />

barriers in plants as first described by G. L. Stebbins.<br />

External barriers<br />

Spatial isolation mechanisms: associated with geographic<br />

distances between two species<br />

Prefertilization reproductive barriers: prevents union <strong>of</strong><br />

gametes. Includes ecological isolation (e.g., spring <strong>and</strong><br />

winter varieties), mechanical isolation (differences in floral<br />

structures), <strong>and</strong> gametic incompatibility<br />

Internal barriers<br />

Postfertilization reproductive barriers: leads to<br />

abnormalities following fertilization (hybrid inviability or<br />

weakness <strong>and</strong> sterility <strong>of</strong> plants)

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