Skip Navigation

This Article
Right arrow Full Text Freely available
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 ISI Web of Science
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 arrow Search for citing articles in:
ISI Web of Science (41)
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Smelt, V. A.
Right arrow Articles by Sim, E.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Smelt, V. A.
Right arrow Articles by Sim, E.
Social Bookmarking
 Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Human Molecular Genetics, 2000, Vol. 9, No. 7 1101-1107
© 2000 Oxford University Press

Expression of arylamine N-acetyltransferases in pre-term placentas and in human pre-implantation embryos

V. A. Smelt, A. Upton, J. Adjaye1, M. A. Payton, S. Boukouvala, N. Johnson, H. J. Mardon2 and E. Sim+

Department of Pharmacology, University of Oxford, Mansfield Road, Oxford OX1 3QT, UK, 1Molecular Embryology Unit, Institute of Child Health, University College London, 30 Guildford Street, London WC1N 1EH, UK and 2Nuffield Department of Obstetrics and Gynaecology, University of Oxford, The Women’s Centre, John Radcliffe Hospital, Oxford OX3 9DU, UK

Arylamine N-acetyltransferases (NATs) catalyse the acetylation from acetyl-CoA of arylamines and hydrazines. There are two human isoenzymes which show polymorphism, and both enzymes are involved in the activation and detoxification of environmental carcinogens and teratogens. The two human isoenzymes NAT1 and NAT2 show different tissue distribution, with human NAT2 being found in liver and intestine whilst human NAT1 is expressed in many tissues including erythrocytes, bladder, lymphocytes and neural tissue, as well as liver and intestine. It has been proposed that NAT1 has an endogenous role in the acetylation of the folate catabolite p-aminobenzoyl-L-glutamate (pABGlu) to produce the major urinary product, N-acetyl-pABGlu. The murine homologue of human NAT1 is known to be concentrated in the neural tube during development. We show here that human NAT1 but not human NAT2 is expressed in pre-implantation embryos at the blastocyst stage and show that NAT1 is also expressed in early human placenta at the earliest available stage, 5.5 weeks. We demonstrate that there is inter-individual variation in NAT1 expression. In view of the role of folate in protecting against neural tube defects, we propose that NAT1 is a candidate risk factor for susceptibility to neural tube defects.

+ To whom correspondence should be addressed. Tel: +44 1865 271596; Fax: +44 1865 271853; Email: esim@molbiol.ox.ac.uk


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
Drug Metab. Dispos.Home page
A. Husain, X. Zhang, M. A. Doll, J. C. States, D. F. Barker, and D. W. Hein
Functional Analysis of the Human N-Acetyltransferase 1 Major Promoter: Quantitation of Tissue Expression and Identification of Critical Sequence Elements
Drug Metab. Dispos., September 1, 2007; 35(9): 1649 - 1656.
[Abstract] [Full Text] [PDF]


Home page
Brief Funct Genomic ProteomicHome page
S. Sudheer and J. Adjaye
Functional genomics of human pre-implantation development
Brief Funct Genomic Proteomic, July 31, 2007; (2007) elm012v1.
[Abstract] [Full Text] [PDF]


Home page
Am. J. Clin. Nutr.Home page
T. Tamura and M. F. Picciano
Folate and human reproduction
Am. J. Clinical Nutrition, May 1, 2006; 83(5): 993 - 1016.
[Abstract] [Full Text] [PDF]


Home page
J. Histochem. Cytochem.Home page
L. Wakefield, V. Cornish, F. Broackes-Carter, and E. Sim
Arylamine N-acetyltransferase 2 Expression in the Developing Heart
J. Histochem. Cytochem., May 1, 2005; 53(5): 583 - 592.
[Abstract] [Full Text] [PDF]


Home page
J. Histochem. Cytochem.Home page
F. Rodrigues-Lima, R. N. Cooper, B. Goudeau, N. Atmane, A.-M. Chamagne, G. Butler-Browne, E. Sim, P. Vicart, and J.-M. Dupret
Skeletal Muscles Express the Xenobiotic-metabolizing Enzyme Arylamine N-acetyltransferase
J. Histochem. Cytochem., June 1, 2003; 51(6): 789 - 796.
[Abstract] [Full Text] [PDF]


Home page
Toxicol SciHome page
C. A. McQueen and B. Chau
Neonatal Ontogeny of Murine Arylamine N-Acetyltransferases: Implications for Arylamine Genotoxicity
Toxicol. Sci., June 1, 2003; 73(2): 279 - 286.
[Abstract] [Full Text] [PDF]


Home page
Am J EpidemiolHome page
G. M. Shaw, V. Nelson, D. M. Iovannisci, R. H. Finnell, and E. J. Lammer
Maternal Occupational Chemical Exposures and Biotransformation Genotypes as Risk Factors for Selected Congenital Anomalies
Am. J. Epidemiol., March 15, 2003; 157(6): 475 - 484.
[Abstract] [Full Text] [PDF]


Home page
Hum Mol GenetHome page
E. Sim, M. Payton, M. Noble, and R. Minchin
An update on genetic, structural and functional studies of arylamine N-acetyltransferases in eucaryotes and procaryotes
Hum. Mol. Genet., October 1, 2000; 9(16): 2435 - 2441.
[Abstract] [Full Text] [PDF]


Home page
Mol Hum ReprodHome page
J. Adjaye and M. Monk
Transcription of homeobox-containing genes detected in cDNA libraries derived from human unfertilized oocytes and preimplantation embryos
Mol. Hum. Reprod., August 1, 2000; 6(8): 707 - 711.
[Abstract] [Full Text] [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.