Could the Leukocyte X Chromosome Inactivation Pattern Be Extrapolated to Hair Bulbs?
Contribuinte(s) |
UNIVERSIDADE DE SÃO PAULO |
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Data(s) |
19/10/2012
19/10/2012
2010
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Resumo |
Background: The androgen receptor gene is located on the X chromosome with a polymorphic tract of CAG repeats that is inversely correlated to the receptor`s transactivation activity. A short CAG tract is associated with hyperandrogenic disorders. In women, one of the X chromosomes is inactivated and the X chromosome inactivation (XCI) pattern varies among tissues. Previous studies of hyperandrogenic disorders only evaluated XCI in leukocytes. Objective: To evaluate whether the XCI pattern in leukocytes could be extrapolated to those in hair bulbs. Material: A total of 58 healthy women were used for this study. DNA was extracted from leukocytes (n = 58 women) and pubic (n = 53 women) and scalp hair (n = 21 women). Methods: Hpa II digested and undigested DNA samples underwent fluorescence PCR GeneScan (R) analysis. Results: A significant and positive correlation of XCI was found between leukocytes and hair bulbs. However, individual comparisons showed that 13 and 19% of the women presented a different leukocyte XCI pattern in pubic hair and similar in leukocytes and hair bulbs of normal women indicating that leukocyte DNA is useful for XCI analysis. However, the XCI pattern could vary among tissues from the same subject, indicating that care should be taken when extrapolating individual leukocyte XCI patterns to other tissue. Copyright (C) 2010 S. Karger AG, Basel FAPESP[06/56028-7] CNPq[301958/2003-3] CNPq[300828/2005-5] |
Identificador |
HORMONE RESEARCH IN PAEDIATRICS, v.73, n.4, p.238-243, 2010 1663-2818 http://producao.usp.br/handle/BDPI/21193 10.1159/000284387 |
Idioma(s) |
eng |
Publicador |
KARGER |
Relação |
Hormone Research in Paediatrics |
Direitos |
restrictedAccess Copyright KARGER |
Palavras-Chave | #X chromosome inactivation #Healthy women #Peripheral leukocyte DNA #Hair bulb DNA #Androgen receptor gene #ANDROGEN-RECEPTOR GENE #CAG REPEAT POLYMORPHISM #POLYCYSTIC-OVARY-SYNDROME #21-HYDROXYLASE DEFICIENCY #FEMALES #DNA #METHYLATION #WOMEN #AGE #TRANSACTIVATION #Endocrinology & Metabolism #Pediatrics |
Tipo |
article original article publishedVersion |