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Introduction to Fungi, Third Edition

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498 BASIDIOMYCOTA<br />

Fig18.9 Diagrammatic<br />

interpretation of a basidiomycete<br />

dolipore/parenthesome septum.<br />

Reprinted from Moore and<br />

Marchant (1972), by copyright<br />

permission of the National Research<br />

Council of Canada.<br />

adjacent <strong>to</strong> the damaged segment (Aylmore et al.,<br />

1984; Markham, 1994).<br />

18.7.4 Plasmogamy, dikaryotization,<br />

clamp connections<br />

When two compatible monokaryotic mycelia<br />

make contact, the hyphal walls separating<br />

them break down and cy<strong>to</strong>plasmic continuity<br />

(i.e. plasmogamy) of the two monokaryons is<br />

established. In Coprinus cinereus and some other<br />

fungi, plasmogamy may also occur following<br />

fusion of an oidium of one mating type with<br />

a hyphal tip of a compatible monokaryon.<br />

Nuclear migration follows and is associated with<br />

the breakdown of the dolipore/parenthesome<br />

complex <strong>to</strong> permit transfer of a compatible<br />

nucleus from one compartment <strong>to</strong> another<br />

(Giesy & Day, 1965; Marchant & Wessels, 1974).<br />

The mycelium which develops after plasmogamy<br />

is dikaryotic and the process of conversion<br />

of a monokaryon <strong>to</strong> a dikaryon is termed<br />

dikaryotization.<br />

Nuclear fusion (i.e. karyogamy) is delayed<br />

until the basidia have formed, and is thus<br />

preceded by a prolonged dikaryotic state. As a<br />

result of nuclear migration, the tip of a dikaryon<br />

contains two nuclei which are of different<br />

mating types in heterothallic basidiomycetes.<br />

The speed of nuclear migration can be much<br />

higher than the hyphal growth rate. Nuclear<br />

migration rates have been measured in a<br />

number of fungi, e.g. Coprinus cinereus

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