Ligase chain reaction assay for human mutations: the Sickle Cell by LCR assay

Author:

Reyes Antonio A1,Carrera Paola2,Cardillo Elena2,Ugozzoli Luis1,Lowery Jimmie D1,Lin Ching-I P1,Go Matthew3,Ferrari Maurizio2,Wallace R Bruce1

Affiliation:

1. DNA Diagnostics Business Unit, Bio-Rad Laboratories, 2000 Alfred Nobel Dr., Hercules, CA 94547

2. IRCCS Clinical Molecular Biology Laboratory, H. San Raffaele, via Olgettina 60, 20132 Milan, Italy

3. Clinical Diagnostics Group, Bio-Rad Laboratories, 2000 Alfred Nobel Dr., Hercules, CA 94547

Abstract

Abstract We can detect the β-globin gene sickle cell mutation by using an assay based on the ligase chain reaction. The simultaneous amplification of the human growth hormone gene in the same reaction serves as a control for the amount of template DNA or amplification efficiency. Ligation products, which are biotinylated at one end and tagged with an arbitrary “tail” sequence at the other, are captured by hybridization to “tail”-complementary oligonucleotides immobilized on polystyrene microwells. The captured ligation products are detected colorimetrically by use of streptavidin–alkaline phosphatase conjugate. In a study of 24 subjects, the assay unequivocally discriminated among normal, carrier, and sickle cell genotypes.

Publisher

Oxford University Press (OUP)

Subject

Biochemistry, medical,Clinical Biochemistry

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