Skip Navigation

This Article
Right arrow FREE Full Text (PDF) Freely available
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Ray, P. F.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Ray, P. F.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Molecular Human Reproduction Vol. 2, NUMBER 3 pp. 213-218, 1996
© European Society of Human Reproduction and Embryology 1996


research-article

Increasing the denaturation temperature during the first cycles of amplification reduced allele dropout from single cells for preimplantation genetic diagnosis

Pierre F. Ray1

Human Embryology Laboratory, Institute of Obstetrics and Gynaecology, Royal postgraduate Medical School, Hammersmith Hospital Du Cane Road, London W12 0NN, UK

To whom correspondence should be addressed at: 1To whom correspondence should be addressed

Single cell polymerase chain reaction (PCR) for preimplantation genetic diagnosis (PGD) needs to be highly efficient and accurate. In some single cells from human embryos presumed to be heterozygous for the {Delta}F508 deletion causing cystic fibrosis (CF), we recently observed random amplification failure of one of the two parental alleles following nested PCR. To investigate allele dropout (ADO), we have examined two different lysis protocols and the effect of altering the denaturation temperature in the primary PCR using single lymphocytes heterozygous for {Delta}F508 or for two {ß-thalassaemia mutations IVS 1 nt 1 (G/T) and 5 (G/C) using a nested PCR protocol to amplify the 5‘ region of the fi-globin gene. Amplification rates were high after lysis in either water or lysis buffer and at all denaturation temperatures studied (≥ 92%). With a typical denaturation temperature (93°C), ADO was detected at both loci. When the denaturation temperature was lowered to 90°C, however, ADO increased substantially and conversely by raising the denaturation temperature to 96°C during the first 10 cycles ADO was reduced but not eliminated. ADO was also reduced with cells in lysis buffer. We suggest that ADO may be caused by a combination of inefficient denaturation and degradation of one of the genomic alleles in the first cycles of PCR. For autosomal recessive conditions in which both parents are carrying the same mutation, ADO would not cause serious misdiagnosis. For compound heterozygotes or autosomal dominant conditions, however, extensive testing of the amplification protocol with single heterozygous cells and individual calibration of each thermocycler for the effect of denaturation temperature on ADO is essential before clinical application.

allele dropout/polymerase chain reaction/preimplantation genetic diagnosis/single cell


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?


This article has been cited by other articles:


Home page
Mol Hum ReprodHome page
Z. Ren, C. Zhou, Y. Xu, J. Deng, H. Zeng, and Y. Zeng
Mutation and haplotype analysis for Duchenne muscular dystrophy by single cell multiple displacement amplification
Mol. Hum. Reprod., June 1, 2007; 13(6): 431 - 436.
[Abstract] [Full Text] [PDF]


Home page
Mol Hum ReprodHome page
P. Burlet, N. Frydman, N. Gigarel, V. Kerbrat, G. Tachdjian, E. Feyereisen, J.-P. Bonnefont, R. Frydman, A. Munnich, and J. Steffann
Multiple displacement amplification improves PGD for fragile X syndrome
Mol. Hum. Reprod., October 1, 2006; 12(10): 647 - 652.
[Abstract] [Full Text] [PDF]


Home page
Hum ReprodHome page
A.R. Thornhill, C.E. deDie-Smulders, J.P. Geraedts, J.C. Harper, G.L. Harton, S.A. Lavery, C. Moutou, M.D. Robinson, A.G. Schmutzler, P.N. Scriven, et al.
ESHRE PGD Consortium 'Best practice guidelines for clinical preimplantation genetic diagnosis (PGD) and preimplantation genetic screening (PGS)'
Hum. Reprod., January 1, 2005; 20(1): 35 - 48.
[Abstract] [Full Text] [PDF]


Home page
Mol Hum ReprodHome page
A. H. Handyside, M. D. Robinson, R. J. Simpson, M. B. Omar, M.-A. Shaw, J.G. Grudzinskas, and A. Rutherford
Isothermal whole genome amplification from single and small numbers of cells: a new era for preimplantation genetic diagnosis of inherited disease
Mol. Hum. Reprod., October 1, 2004; 10(10): 767 - 772.
[Abstract] [Full Text] [PDF]


Home page
Mol Hum ReprodHome page
M. Tachataki, R. M.L. Winston, and D. M. Taylor
Quantitative RT-PCR reveals tuberous sclerosis gene, TSC2, mRNA degradation following cryopreservation in the human preimplantation embryo
Mol. Hum. Reprod., October 1, 2003; 9(10): 593 - 601.
[Abstract] [Full Text] [PDF]


Home page
Mol Hum ReprodHome page
F. Fiorentino, M.C. Magli, D. Podini, A.P. Ferraretti, A. Nuccitelli, N. Vitale, M. Baldi, and L. Gianaroli
The minisequencing method: an alternative strategy for preimplantation genetic diagnosis of single gene disorders
Mol. Hum. Reprod., July 1, 2003; 9(7): 399 - 410.
[Abstract] [Full Text] [PDF]


Home page
Mol Hum ReprodHome page
W. Piyamongkol, M. G. Bermudez, J. C. Harper, and D. Wells
Detailed investigation of factors influencing amplification efficiency and allele drop-out in single cell PCR: implications for preimplantation genetic diagnosis
Mol. Hum. Reprod., July 1, 2003; 9(7): 411 - 420.
[Abstract] [Full Text] [PDF]


Home page
Mol Hum ReprodHome page
C. Vrettou, M. Tzetis, J. Traeger-Synodinos, G. Palmer, and E. Kanavakis
Multiplex sequence variation detection throughout the CFTR gene appropriate for preimplantation genetic diagnosis in populations with heterogeneity of cystic fibrosis mutations
Mol. Hum. Reprod., September 1, 2002; 8(9): 880 - 886.
[Abstract] [Full Text] [PDF]


Home page
Mol Hum ReprodHome page
P. F. Ray, N. Frydman, T. Attie, S. Hamamah, V. Kerbrat, G. Tachdjian, S. Romana, M. Vekemans, R. Frydman, and A. Munnich
Birth of healthy female twins after preimplantation genetic diagnosis of cystic fibrosis combined with gender determination
Mol. Hum. Reprod., July 1, 2002; 8(7): 688 - 694.
[Abstract] [Full Text] [PDF]


Home page
J. Mol. Diagn.Home page
A. R. Thornhill and K. Snow
Molecular Diagnostics in Preimplantation Genetic Diagnosis
J. Mol. Diagn., February 1, 2002; 4(1): 11 - 29.
[Full Text] [PDF]


Home page
J. Med. Genet.Home page
E Kanavakis and J Traeger-Synodinos
Preimplantation genetic diagnosis in clinical practice
J. Med. Genet., January 1, 2002; 39(1): 6 - 11.
[Abstract] [Full Text] [PDF]


Home page
Mol Hum ReprodHome page
G. Daniels, R. Pettigrew, A. Thornhill, S. Abbs, A. Lashwood, F. O'Mahony, C. Mathew, A. Handyside, and P. Braude
Six unaffected livebirths following preimplantation diagnosis for spinal muscular atrophy
Mol. Hum. Reprod., October 1, 2001; 7(10): 995 - 1000.
[Abstract] [Full Text] [PDF]


Home page
Mol Hum ReprodHome page
N.L. Dean, S.L. Tan, and A. Ao
The development of preimplantation genetic diagnosis for myotonic dystrophy using multiplex fluorescent polymerase chain reaction and its clinical application
Mol. Hum. Reprod., September 1, 2001; 7(9): 895 - 901.
[Abstract] [Full Text] [PDF]


Home page
Mol Hum ReprodHome page
P. F. Ray, M. Vekemans, and A. Munnich
Single cell multiplex PCR amplification of five dystrophin gene exons combined with gender determination
Mol. Hum. Reprod., May 1, 2001; 7(5): 489 - 494.
[Abstract] [Full Text] [PDF]


Home page
Mol Hum ReprodHome page
I. Eftedal, M. Schwartz, H. Bendtsen, A.N. Andersen, and S. Ziebe
Single intragenic microsatellite preimplantation genetic diagnosis for cystic fibrosis provides positive allele identification of all CFTR genotypes for informative couples
Mol. Hum. Reprod., March 1, 2001; 7(3): 307 - 312.
[Abstract] [Full Text] [PDF]


Home page
Mol Hum ReprodHome page
D. Blake, S. L. Tan, and A. Ao
Assessment of multiplex fluorescent PCR for screening single cells for trisomy 21 and single gene defects
Mol. Hum. Reprod., December 1, 1999; 5(12): 1166 - 1175.
[Abstract] [Full Text] [PDF]


Home page
J Law Med EthicsHome page
R. J. Tasca and M. E. McClure
The Emerging Technology and Application of Preimplantation Genetic Diagnosis
J. Law Med. Ethics, March 1, 1998; 26(1): 7 - 16.
[PDF]



Disclaimer:
Please note that abstracts for content published before 1996 were created through digital scanning and may therefore not exactly replicate the text of the original print issues. All efforts have been made to ensure accuracy, but the Publisher will not be held responsible for any remaining inaccuracies. If you require any further clarification, please contact our Customer Services Department.