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Principles of Plant Genetics and Breeding

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222 CHAPTER 13<br />

the chromosomes <strong>of</strong> one genome may share a function<br />

in common with some chromosomes in a different<br />

genome. Chromosomes from two genomes are said<br />

to be homeologous when they are similar but not<br />

homologous (identical).<br />

Most alloploids have evolved certain genetic systems<br />

that ensure that pairing occurs between chromosomes<br />

<strong>of</strong> the same genome. A classic example occurs in wheat<br />

(2n = 6x = 42) in which a gene on chromosome 5B,<br />

designated Ph, enforces this diploid-like paring within<br />

genomes <strong>of</strong> the alloploid. When this gene is absent,<br />

pairing between homeologous chromosomes, as well as<br />

corresponding chromosomes <strong>of</strong> the three genomes,<br />

occurs, resulting in the formation <strong>of</strong> multivalents at<br />

meiosis I.<br />

Alloploids exhibit a variety <strong>of</strong> meiotic features.<br />

Sometimes chromosomes pair as bivalents <strong>and</strong> thereby<br />

produce disomic ratios. Where the component genomes<br />

have genes in common, duplicate factor ratios will<br />

emerge from meiosis, an event that sometimes is an<br />

indication <strong>of</strong> alloploid origin <strong>of</strong> the species. Whereas<br />

significant duplications <strong>of</strong> genetic material have been<br />

found in wheat, the genomes <strong>of</strong> upl<strong>and</strong> cotton have<br />

little duplication. Tetrasomic ratios are expected for<br />

some loci where multivalent associations are found in<br />

allotetraploids.<br />

Industry highlights<br />

Application <strong>of</strong> tissue culture for tall wheatgrass improvement<br />

Kany<strong>and</strong> Mat<strong>and</strong> <strong>and</strong> George Acquaah<br />

Department <strong>of</strong> Agriculture <strong>and</strong> Applied Sciences, Langston University, Langston, OK 73050, USA<br />

Introduction<br />

Cultivar “Jose” <strong>of</strong> tall wheatgrass (Thinopyrum ponticum Podp.) is a perennial, cross-pollinating, bunchgrass, used as a cool-season<br />

livestock forage. It is adapted to the Oklahoma environment primarily because <strong>of</strong> its relative ease-to-establish <strong>and</strong> tolerance <strong>of</strong> a<br />

wide range <strong>of</strong> soil pH. This bunchgrass can produce high levels <strong>of</strong> dry matter per season (Coleman 1999) <strong>and</strong> exhibit superior<br />

characteristics such as high biomass production, persistence through extended periods <strong>of</strong> grazing, <strong>and</strong> saline, flood, <strong>and</strong> drought<br />

tolerance (Moser et al. 1996; Coleman 1999; Redmon 1999). Although used successfully to improve plants for many years, limitations<br />

associated with traditional breeding approaches coupled with the large genome <strong>of</strong> tall wheatgrass (2n = 10x = 70) makes it<br />

improbable <strong>and</strong> difficult to improve this crop by relying on traditional breeding methods alone (Kindiger 2002). Because tissue<br />

culture is a prerequisite for the successful integration <strong>of</strong> classic plant breeding <strong>and</strong> genetic engineering for genetic crop improvement,<br />

researchers at Langston University, Oklahoma, <strong>and</strong> the US Department <strong>of</strong> Agriculture–Agricultural Research Service<br />

(USDA-ARS) Grazingl<strong>and</strong>s Research Laboratory at El Reno, Oklahoma, collaborated to develop an efficient in vitro method for<br />

propagating this crop as an additional tool for its improvement. The discussion in this box focuses primarily on a one-step, reliable<br />

approach to microclone tall wheatgrass for germplasm development for its improvement; it also highlights cautions <strong>and</strong> pitfalls<br />

associated with the proposed method in particular, <strong>and</strong> tissue culture in general. This one-step method may be adapted for tissue<br />

culture research in other forage species.<br />

Basic approaches to plant regeneration<br />

There are a variety <strong>of</strong> ways to regenerate plants in vitro, but all <strong>of</strong> them can be grouped into two basic approaches, direct <strong>and</strong><br />

indirect.<br />

1 Direct plant regeneration. Direct plant regeneration occurs without an intervening callus phase. Potential growth focal<br />

structures consist <strong>of</strong> apical <strong>and</strong> axillary meristems, nodes, leaves, stem, roots, zygotic embryos, cotyledons, the whole seed,<br />

<strong>and</strong> other structures. These organs can be excised from the mother plant to induce somatic embryos or adventitious shoots,<br />

or both, without an intervening callus phase.<br />

2 Indirect plant regeneration. This process is characteristic <strong>of</strong> the callus phase mediation for somatic plant formation from<br />

explants. Explants similar to those listed for direct plant regeneration can also be used to induce somatic embryos or adventitious<br />

shoots, or both, via callus formation.

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