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Rapid detection of aneuploidies by microsatellite and the quantitative fluorescent polymerase chain reaction
Author(s) -
Adinolfi Matteo,
Pertl Barbara,
Sherlock Jon
Publication year - 1997
Publication title -
prenatal diagnosis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.956
H-Index - 97
eISSN - 1097-0223
pISSN - 0197-3851
DOI - 10.1002/(sici)1097-0223(199712)17:13<1299::aid-pd297>3.0.co;2-h
Subject(s) - prenatal diagnosis , microsatellite , polymerase chain reaction , biology , multiplex , aneuploidy , cell free fetal dna , chorionic villi , microbiology and biotechnology , multiplex polymerase chain reaction , autosome , fetus , chromosome , genetics , pregnancy , gene , allele
Abstract Several studies have been performed to assess the diagnostic value of using small tandem repeat (STR) markers and quantitative fluorescent polymerase chain reaction (QF‐PCR) assays for the rapid detection of aneuploidies involving chromosomes 21, 18, 13 (Mansfield, 1993; Pertl et al. , 1994, 1996; Adinolfi et al. , 1995a). The results of these investigations have documented the diagnostic advantages of this approach to perform prenatal tests using amniotic and chorionic samples, or fetal nucleated cells retrieved from peripheral maternal blood or endocervical samples. The use of two or more STR markers for each autosome facilitates the diagnosis of aneuploidies, while avoiding the need to employ internal non‐polymorphic markers. Multiplex quantitative fluorescent analyses can be performed in about six hours from the collection of the samples and, although targeted to specific abnormalities, they can exclude the presence of the most frequent chromosomal disorders. QF‐PCR can be exploited to analyse DNA present in single or clumps of cells and thus to perform prenatal diagnoses on maternal peripheral blood or transcervical cell samples and on preimplantation embryos. © 1997 by John Wiley & Sons, Ltd.