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Principles of Plant Genetics and Breeding

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BREEDING SORGHUM 513<br />

Kansas State University, Texas A&M University, <strong>and</strong> USDA. These public programs do not produce or sell hybrids, but they<br />

develop parental lines <strong>and</strong> germplasms that are used by private industry in commercial hybrid production. In addition, public<br />

research programs in sorghum conduct research in long-term projects such as the introgression <strong>and</strong> development <strong>of</strong> new<br />

germplasm that may provide useful traits in the future.<br />

The Texas Agricultural Experiment Station (TAES) sorghum breeding program located at Texas A&M University in College<br />

Station, Texas is part <strong>of</strong> a multiproject, multilocation sorghum improvement program supported by the TAES. Sorghum breeders<br />

work in conjunction with plant pathologists, entomologists, <strong>and</strong> grain quality <strong>and</strong> molecular geneticists to create an effective <strong>and</strong><br />

important research <strong>and</strong> application oriented team. In terms <strong>of</strong> the sorghum breeding program at College Station, the breeding<br />

program has several objectives: (i) develop <strong>and</strong> release germplasm <strong>and</strong> parental lines with improved adaptability, yield, quality,<br />

<strong>and</strong> stress resistances; (ii) conduct research that increases our underst<strong>and</strong>ing <strong>and</strong> knowledge <strong>of</strong> sorghum breeding <strong>and</strong> genetics;<br />

<strong>and</strong> (iii) train undergraduate <strong>and</strong> graduate students in plant breeding.<br />

Methodology <strong>of</strong> the TAES sorghum breeding program at College Station<br />

For improved hybrids, new <strong>and</strong> improved parental lines must be developed. First, genetic variability must be developed through<br />

the selection <strong>and</strong> hybridization <strong>of</strong> parent material. This is a crucial step in the process. Usually elite germplasm is crossed to other<br />

material (elite lines, germplasm, genetic stocks) to correct a perceived deficiency in the elite material. For example, if an otherwise<br />

good A/B pair is susceptible to lodging, it will be<br />

Summer Year 0<br />

Winter Year 0<br />

Summer Year 1<br />

Summer Year 2<br />

Summer Year 3<br />

Summer Year 4<br />

<strong>Breeding</strong> crosses are made;<br />

∼200 annually<br />

Weslaco, Texas<br />

self-pollinated;<br />

∼200 annually<br />

College Station (CS), Beeville, Texas<br />

200 populations <strong>and</strong> 15 rows/population;<br />

∼3,000 plots annually<br />

One environment/per selection<br />

Either CS, Corpus Christi (CC)<br />

or Lubbock (LB), Texas<br />

∼5,000 plots annually<br />

Genotypes are shifted among<br />

environments (CS or CC)<br />

∼2,000 plots annually<br />

Multiple environments (CC, CS, <strong>and</strong> LB)<br />

Testcross hybrids made in CS, <strong>and</strong><br />

sterilization (for B-lines) begun in CS<br />

∼500 lines annually<br />

P 1 × P 2<br />

Figure 2 Pedigree breeding scheme used by the TAES<br />

sorghum breeding program at College Station, Texas. This<br />

scheme is used for the development <strong>of</strong> new B- <strong>and</strong> R-lines <strong>and</strong><br />

germplasm. Initial crosses are made using either plastic bag<br />

crosses or h<strong>and</strong> emasculations. Open-pollinated selections are<br />

made in each generation until the F 5 where the plot is selfpollinated<br />

<strong>and</strong> used to make testcross hybrids. At the F 5<br />

generation, new B-lines enter sterilization <strong>and</strong> testcrossing while<br />

new R-lines are evaluated in testcrosses.<br />

F 1<br />

F 2<br />

F 2:3<br />

F 3:4<br />

F 4:5<br />

hybridized with several different sources <strong>of</strong> lodging<br />

resistance with the goal <strong>of</strong> producing a new A/B pair<br />

with improved lodging resistance. In our program, the<br />

A/B program is managed separately from the R-line<br />

program to maintain heterosis between the two groups<br />

<strong>and</strong> keep the fertility restoration <strong>and</strong> maintenance<br />

genetics separate. Based on the considerations listed<br />

above, specific crosses are made using the methodology<br />

described by Rooney (2004). These F 1 progeny are<br />

self-pollinated to produce an F 2 population.<br />

Once F 2 populations are created, our program utilizes<br />

a pedigree breeding approach for the development<br />

<strong>of</strong> inbred lines (Figure 2). From the F 2 generation<br />

until the F 5 generation (in which uniform lines are<br />

selected), the progeny rows are grown <strong>and</strong> panicles in<br />

the rows are visually selected on the basis <strong>of</strong> agronomic<br />

desirability, pest resistance, <strong>and</strong> abiotic stress<br />

tolerance. F 5 lines that are phenotypically uniform are<br />

testcrossed to measure their general <strong>and</strong> specific combining<br />

ability <strong>and</strong> their suitability as parent lines in<br />

hybrid combinations.<br />

The appropriate time for the selection <strong>of</strong> specific<br />

traits is dependent on the heritability <strong>of</strong> the trait <strong>and</strong><br />

the environments in which the selection occurs. In<br />

our program, traits with higher heritability (maturity,<br />

height, grain color, etc.) are selected in the early generations<br />

while traits with lower heritability (yield,<br />

drought tolerance, disease <strong>and</strong> insect resistance) are<br />

selected in more advanced generations. These more<br />

complexly inherited traits must also be screened in<br />

multiple environments, because these traits may not<br />

be expressed in any given environment. Evaluation in<br />

multiple environments is crucial to the development<br />

<strong>of</strong> widely adapted sorghum genotypes. In our program,<br />

we use three basic regions for inbred selection:<br />

south Texas, central Texas, <strong>and</strong> the Texas high plains<br />

(Figure 3). These regions are each unique <strong>and</strong> force<br />

different selection pressures on the material grown<br />

therein. For example, our south Texas nurseries are<br />

rainfed <strong>and</strong> subject to drought stress <strong>and</strong> consistent<br />

disease pressure. In addition, this region is good for<br />

selecting genotypes that perform well in subtropical

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