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Heterokaryons can arise in two ways. First, when
a mutation occurs in any of the nuclei of a hypha
and the mutated nucleus proliferates along with the
wild-type nuclei. This must happen very often, but
a stable, functional heterokaryon will develop only
if the genetically different nuclei proliferate in the
apical cells so that all the newly formed hyphae con-
tain both types. A second way in which heterokaryons
arise is by tip-to-tip fusion (anastomosis) of the hyphae
of two strains (see Fig. 3.6). Again, the nuclei would
need to proliferate in the apical cells to form a stable
heterokaryon.
Most experimental studies on heterokaryosis have
involved the pairing of strains with defined mutations,
such as amino acid auxotrophs. The heterokaryon
will then behave as a prototroph, capable of growing
on minimal medium. The most interesting feature
in these cases is that the ratio of nuclear genotypes
can vary within wide limits and is influenced by envir-
onmental conditions. So, at least in theory, a single
heterokaryotic strain can change the frequency distri-
bution of its nuclear types in response to selection
pressure. This has been demonstrated experimentally
in classic experiments by Jinks (1952), as shown in
Table 9.3. A heterokaryon of the apple-rot fungus,
Penicillium cyclopiumwas constructed by allowing two
different homokaryons to fuse. Then the heterokaryon
was grown on agar containing different proportions
of apple pulp or minimal nutrient medium. The ratio
of nuclear types (which we will call A and B) in the
heterokaryon was assessed by testing random samples
of uninucleate (homokaryotic) spores from the colony.
When the heterokaryon was grown on apple-pulp
medium the proportion of B-type nuclei was very
high, but as the amount of apple pulp was lowered
so the proportion of A-type nuclei increased, and
dramatically so when the heterokaryon was grown on
minimal medium. Other experiments of this type


have shown that the nuclear ratio in a heterokaryon
can vary by up to 1000 : 1 in either direction. If
this happens at all commonly in nature it would
contribute significantly to continuous variationand
selection of the best adapted nuclear ratio.

How do heterokaryons break down?

Heterokaryons can break down in two ways (Fig. 9.5)


  • either during the production of uninucleate spores,
    or when branches arise that contain only one nuclear
    type. Many common fungi produce uninucleate spores,
    often by repeated mitotic division of a “mother” nucleus
    in a phialide – Aspergillus, Penicillium, Trichoderma,
    Gliocladium, etc. (Fig. 9.5a(i) ). Multinucleate spores can
    also be produced from phialides, if a single nucleus
    enters the developing spore and then divides to pro-
    duce several nuclei. For example, this is seen in many
    Fusariumspecies (Fig. 9.5b). But some other fungi (e.g.
    Neurospora, Fig. 9.5c) produce conidia directly from
    multinucleate hyphal tips or buds, and these spores will
    be either homokaryotic or heterokaryotic, depending
    on whether the cells that produced them were homo-
    karyotic or heterokaryotic.
    Heterokaryons also break down if a branch arises that,
    by chance, contains only one nuclear genotype. This
    branch can produce further branches and eventually
    give rise to a homokaryotic sector of the colony
    (Fig. 9.5a(ii)). If the homokaryon is favored more than
    the heterokaryon in the prevailing environment then
    it will expand to occupy progressively more of the
    colony margin; if not favored it will be suppressed.
    Figure 9.5d shows an example of this, where a fungal
    colony was initially darkly pigmented (with daily zones
    of white aerial hyphae). Two light-colored sectors
    soon developed and because of their faster growth
    they progressively expanded. This type of sectoring
    is quite often seen in fungal colonies – either as


FUNGAL GENETICS, MOLECULAR GENETICS, AND GENOMICS 165

Table 9.3Effects of composition of the growth medium on the ratio of nuclear types in a heterokaryon of Penicillium
cyclopium. (Data from Jinks 1952.)


% of nuclei in Relative growth rates of
Composition of medium (%) the heterokaryon homokaryons A and B

Minimal nutrients Apple pulp Type A Type B A : B


0 100 8.6 91.4 0.47 : 1

20 80 7.8 92.2 0.53 : 1

40 60 11.1 88.9 0.54 : 1

60 40 12.7 87.3 0.67 : 1

80 20 13.5 86.5 1 : 1

100 0 51.8 48.2 1.56 : 1
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