A widely applicable strategy for single cell genotyping of beta-thalassaemia mutations using DGGE analysis: Application to preimplantation genetic diagnosis

Επιστημονική δημοσίευση - Άρθρο Περιοδικού uoadl:3052576 21 Αναγνώσεις

Μονάδα:
Ερευνητικό υλικό ΕΚΠΑ
Τίτλος:
A widely applicable strategy for single cell genotyping of
beta-thalassaemia mutations using DGGE analysis: Application to
preimplantation genetic diagnosis
Γλώσσες Τεκμηρίου:
Αγγλικά
Περίληψη:
Preimplantation genetic diagnosis (PGD) allows the selection of
unaffected IVF embryos for transfer in couples that are at risk for
transmitting genetic diseases. For monogenic diseases, polymerase chain
reaction (PCR)-based diagnosis is usually performed on single
blastomeres. In Greece, up to 10 per cent of the population are carriers
for beta-thalassaemia and related haemoglobinopathies, and more than 20
pathological mutations in the beta-globin gene have been described. In
this study we report a strategy which includes a first round of PCR,
allowing subsequent nested PCR and DGGE analysis for at least 95 per
cent of beta-thalassaemia major genotypes in the Greek population. The
use of DCGE for beta-globin genotype analysis is advantageous: it
facilitates simultaneous analysis of more than one mutation in a single
PCR fragment, it detects the presence of normal alleles and monitors the
occurrence of allelic drop-out (ADO) through the expectation that
heterozygous samples have more than one electrophoretic band on DGGE
analysis. The optimization, accuracy and reliability of the method was
evaluated by genotyping 325 single blastomeres, 110 amniocytes and 55
lymphocytes. Results confirmed that PCR efficiency and occurrence of ADO
are improved by higher denaturation temperatures in the first cycles of
first-round PCR, influenced by the size of the fragment amplified in the
first round of PCR and additionally by the quality and type of cells
being genotyped. The proposed strategy was accurate and reliable, and
thus for application to PGD should ensure the transfer of unaffected
embryos. Furthermore it is widely applicable in most of the populations
worldwide where beta-thalassaemia is common. Copyright (C) 1999 John
Wiley & Sons, Ltd.
Έτος δημοσίευσης:
1999
Συγγραφείς:
Vrettou, C
Palmer, G
Kanavakis, E
Tzetis, M
Antoniadi, T
and Mastrominas, M
Traeger-Synodinos, J
Περιοδικό:
Prenatal Diagnosis
Εκδότης:
Wiley
Τόμος:
19
Αριθμός / τεύχος:
13
Σελίδες:
1209-1216
Λέξεις-κλειδιά:
preimplantation genetic diagnosis; beta-thalassaemia; PCR amplification;
DGGE analysis
DOI:
10.1002/(SICI)1097-0223(199912)19:13<1209::AID-PD722>3.0.CO;2-6
Το ψηφιακό υλικό του τεκμηρίου δεν είναι διαθέσιμο.