Development of a real-time PCR genotyping assay to identify high oleic acid peanuts (Arachis hypogaea L.)

作者：Barkley Noelle A; Chamberlin Kelly D Chenault; Wang Ming Li^*; Pittman Roy N

来源：Molecular Breeding, 2010, 25(3): 541-548.

DOI：10.1007/s11032-009-9338-z

• Real-time PCR
• Oleic acid (C18:1)
• Peanut (Arachis hypogaea L.)
• Gas chromatography
• Indel
• Microsomol-oleoyl PC desaturase

Oleic acid, a monounsaturated, omega-9 fatty acid found in peanut (Arachis hypogaea L.) oil is an important seed quality trait because it provides increased shelf life, improved flavor, enhanced fatty acid composition, and has a beneficial effect on human health. Hence, a concentrated effort has been put forth on developing peanut cultivars that have high oleic acid (> 74%) and a low amount (< 10%) of linoleic acid, a polyunsaturated omega-6 fatty acid. A main bottleneck, however, in breeding research is fast selection of the trait(s) of interest. Therefore, in an effort to expedite breeding efforts, a real-time PCR genotyping assay was developed to rapidly identify the wild type and the mutant allele that are responsible for normal or high levels of oleic acid, respectively in peanut seeds. This test utilizes two TaqMan(A (R)) probes to detect the presence of an indel (insertion/deletion) in FAD2B and can be employed on DNA extracted from either seeds or leaves. The presence of the insertion (mutant allele) in fad2B causes a frameshift downstream in the coding sequence that ultimately alters the mRNA transcript level, and thus, decreases the activity of microsomal oleoyl-PC desaturase enzyme which converts oleic acid (C18:1) to linoleic acid (C18:2). Validation of the real-time assay was carried out by quantitatively evaluating the fatty acid composition by gas chromatography (GC). Overall, this real-time PCR assay facilitates the identification of progeny carrying the high oleic acid alleles, and thus, allows early elimination of undesirable non-high oleic acid lines in segregating populations.

• 出版日期2010-3