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Principles of Plant Genetics and Breeding

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SEXUAL HYBRIDIZATION AND WIDE CROSSES IN PLANT BREEDING 177<br />

Insecticide use has been the primary means <strong>of</strong><br />

controlling wireworm damage. However, insecticides<br />

currently used for wireworm control may lose their<br />

registration in the future. Genetic resistance to wireworm<br />

could be an important component <strong>of</strong> an integrated<br />

pest management (IPM) program, <strong>and</strong> it was<br />

decided to evaluate the progeny <strong>of</strong> S. etuberosum for<br />

wireworm resistance.<br />

In collaboration with Dr Juan Alvarez, an entomologist<br />

with the University <strong>of</strong> Idaho, one BC 1 <strong>and</strong> four<br />

BC 2 clones derived from the S. etuberosum somatic<br />

hybrids were evaluated for wireworm resistance; comparisons<br />

<strong>of</strong> these clones were made relative to a susceptible<br />

cultivar, “Russet Burbank”. An additional<br />

treatment also was included in the evaluation; susceptible<br />

“Russet Burbank” was treated with Genesis®, an<br />

insecticide commonly used for wireworm control.<br />

Four <strong>of</strong> the five backcross clones had a percentage <strong>of</strong><br />

damaged tubers comparable to or lower than that<br />

observed with the use <strong>of</strong> Genesis®. Wireworm entry<br />

points or “holes” per tuber among the five clones were<br />

comparable to the numbers observed with the use <strong>of</strong><br />

Genesis®.<br />

The resistance <strong>of</strong> two <strong>of</strong> the five clones was<br />

attributable to high levels <strong>of</strong> certain chemical compounds<br />

naturally produced in the tuber called glycoalkaloids.<br />

Total tuber glycoalkaloid concentrations<br />

need to be less than 20 mg/100 g tuber fresh weight<br />

for safe consumption by humans – these two highly<br />

resistant clones had levels ≥ 47 mg/100 g. However, the remaining three clones had acceptable total tuber glycoalkaloid levels <strong>of</strong><br />

≤ 13 mg/100 g; all three, relative to susceptible “Russet Burbank”, had reduced wireworm entry damage <strong>and</strong> two <strong>of</strong> the three<br />

had a reduced percentage <strong>of</strong> wireworm-damaged tubers. These data indicate that high total tuber glycoalkaloid levels are not<br />

necessary for conferring wireworm resistance – an important finding if wireworm-resistant potato cultivars with acceptable<br />

glycoalkaloid levels are to be developed.<br />

References<br />

etb txb SH Kat Atl BC1l--------BC2--------------l<br />

Figure 3 Segregation <strong>of</strong> a RFLP (restriction fragment length<br />

polymorphism) specific to S. etuberosum; the RFLP probe used<br />

was TG65. The arrow indicates the RFLP unique to S.<br />

etuberosum that also is present in the somatic hybrid (SH), BC 1 ,<br />

<strong>and</strong> two <strong>of</strong> six BC 2 . This molecular marker is not present in the<br />

S. tuberosum × S. berthaultii fusion parent (txb) or the potato<br />

cultivars “Katahdin” (Kat) or “Atlantic” (Atl) that were used as<br />

parents in the generation <strong>of</strong> the backcross progeny. Numbers<br />

on the side are approximations <strong>of</strong> the RFLP fragment sizes.<br />

Correll, D.S. 1962. The potato <strong>and</strong> its wild relatives. Texas Research Foundation, Renner, TX, 606 pp.<br />

Novy, R.G., <strong>and</strong> J.P. Helgeson. 1994a. Somatic hybrids between Solanum etuberosum <strong>and</strong> diploid, tuber bearing Solanum<br />

clones. Theor. Appl. Genet. 89:775–782.<br />

Novy, R.G., <strong>and</strong> J.P. Helgeson. 1994b. Resistance to potato virus Y in somatic hybrid between Solanum etuberosum <strong>and</strong><br />

S. tuberosum × S. berthaultii hybrid. Theor. Appl. Genet. 89:783–786.<br />

Novy, R.G., A. Nasruddin, D.W. Ragsdale, <strong>and</strong> E.B. Radcliffe. 2002. Genetic resistances to potato leafroll virus, potato virus Y,<br />

<strong>and</strong> green peach aphid in progeny <strong>of</strong> Solanum etuberosum. Am. J. Potato Res. 79:9–18.<br />

Overcoming barriers to fertilization<br />

1 Conduct reciprocal crosses. Generally, it is recommended<br />

to use the parent with the larger chromosome<br />

number as the female in a wide cross for a<br />

higher success rate. This is because some crosses are<br />

successful only in one direction. Hence, where there<br />

is no previous information about crossing behavior, it<br />

is best to cross in both directions.<br />

2 Shorten the length <strong>of</strong> the style. The pollen tube <strong>of</strong> a<br />

short-styled species may not be able to grow through<br />

a long style to reach the ovary. Thus, shortening a<br />

long style may improve the chance <strong>of</strong> a short pollen<br />

tube reaching the ovary. This technique has been successfully<br />

tried in corn.<br />

3 Apply growth regulators. Chemical treatment <strong>of</strong><br />

the pistil with growth-promoting substances (e.g.,<br />

naphthalene acetic acid, gibberellic acid) tends to

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