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Theoretical and Experimental DNA Computation (Natural ...

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154 6 Cellular Computing<br />

x<br />

y<br />

z<br />

x<br />

(a) (b) (c)<br />

Fig. 6.6. Excision<br />

y<br />

z<br />

x z<br />

made (Fig. 6.6b). The pointers connecting the MDSs then join them together,<br />

while the IES self-anneals to yield a circular molecule (Fig. 6.6c).<br />

The second operation is known as hairpin, inverted repeat excision, <strong>and</strong><br />

is used in the situation where a pointer has two occurrences, one of which<br />

is inverted. The molecule folds into a hairpin structure (Fig. 6.7a) with the<br />

pointer <strong>and</strong> its inversion aligned, cuts are made (Fig. 6.7b) <strong>and</strong> the inverted<br />

sequence is reinserted (Fig. 6.7c), yielding a single molecule.<br />

(a)<br />

(c)<br />

Fig. 6.7. Inversion<br />

The third <strong>and</strong> final operation is double-loop, alternating direct repeat excision/reinsertion.<br />

This operation is applicable in situations where two repeats<br />

of two pointers have interleaving occurrences on the same str<strong>and</strong>. The double<br />

loop folding is made such that the two pairs of identical pointer occurrences<br />

are aligned (Fig. 6.8a), cuts are made (Fig. 6.8b) <strong>and</strong> the recombination takes<br />

place, yielding the molecule from Fig. 6.8c.<br />

The process by which gene assembly takes place using these operations<br />

<strong>and</strong> the computational properties of the system are discussed in detail in [56].<br />

However, the important difference between this model <strong>and</strong> that of L<strong>and</strong>weber<br />

<strong>and</strong> Kari is that it is more concerned with the mechanics of the gene assembly<br />

process than the computational power of an abstraction of the natural system.<br />

y<br />

(b)

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