Evidence from autoimmune thyroiditis of skewed X-chromosome inactivation in female predisposition to autoimmunity

被引:92
作者
Ozcelik, Tayfun
Uz, Elif
Akyerli, Cemaliye B.
Bagislar, Sevgi
Mustafa, Chigdem A.
Gursoy, Alptekin
Akarsu, Nurten
Toruner, Gokce
Kamel, Nuri
Gullu, Sevim
机构
[1] Bilkent Univ, Fac Sci, Dept Mol Biol & Genet, TR-06800 Ankara, Turkey
[2] Ankara Univ, Sch Med, Dept Endocrinol & Metab Dis, TR-06100 Ankara, Turkey
[3] Hacettepe Univ, Fac Med, Dept Pediat, Pediat Hematol Unit,Gene Mapping Lab, TR-06100 Ankara, Turkey
[4] Univ Med & Dent New Jersey, New Jersey Med Sch, Ctr Human & Mol Genet, Newark, NJ 07103 USA
关键词
X chromosome inactivation; autoimmune thyroid disease; female predisposition to autoimmunity;
D O I
10.1038/sj.ejhg.5201614
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The etiologic factors in the development of autoimmune thyroid diseases (AITDs) are not fully understood. We investigated the role of skewed X-chromosome inactivation (XCI) mosaicism in female predisposition to AITDs. One hundred and ten female AITDs patients ( 81 Hashimoto's thyroiditis ( HT), 29 Graves' disease (GD)), and 160 female controls were analyzed for the androgen receptor locus by the HpaII/polymerase chain reaction assay to assess XCI patterns in DNA extracted from peripheral blood cells. In addition, thyroid biopsy, buccal mucosa, and hair follicle specimens were obtained from five patients whose blood revealed an extremely skewed pattern of XCI, and the analysis was repeated. Skewed XCI was observed in DNA from peripheral blood cells in 28 of 83 informative patients (34%) as compared with 10 of 124 informative controls (8%, P < 0.0001). Extreme skewing was present in 16 patients (19%), but only in three controls (2.4%, P < 0.0001). The buccal mucosa, and although less marked, the thyroid specimens also showed skewing. Analysis of two familial cases showed that only the affected individuals demonstrate skewed XCI patterns. Based on these results, skewed XCI mosaicism may play a significant role in the pathogenesis of AITDs.
引用
收藏
页码:791 / 797
页数:7
相关论文
共 30 条
[1]   Merlin-rapid analysis of dense genetic maps using sparse gene flow trees [J].
Abecasis, GR ;
Cherny, SS ;
Cookson, WO ;
Cardon, LR .
NATURE GENETICS, 2002, 30 (01) :97-101
[2]   Microchimerism - An investigative frontier in autoimmunity and transplantation [J].
Adams, KM ;
Nelson, JL .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2004, 291 (09) :1127-1131
[3]  
ALLEN RC, 1992, AM J HUM GENET, V51, P1229
[4]  
Ban Yoshiyuki, 2005, Clin Dev Immunol, V12, P47, DOI 10.1080/17402520400008897
[5]   Linkage analysis of candidate genes in autoimmune thyroid disease. II. Selected gender-related genes and the X-chromosome [J].
Barbesino, G ;
Tomer, Y ;
Concepcion, ES ;
Davies, TF ;
Greenberg, DA .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1998, 83 (09) :3290-3295
[6]   Familial nonrandom inactivation linked to the X inactivation centre in heterozygotes manifesting haemophilia A [J].
Bicocchi, MP ;
Migeon, BR ;
Pasino, M ;
Lanza, T ;
Bottini, F ;
Boeri, E ;
Molinari, AC ;
Corsolini, F ;
Morerio, C ;
Acquila, M .
EUROPEAN JOURNAL OF HUMAN GENETICS, 2005, 13 (05) :635-640
[7]   High frequency of skewed X-chromosome inactivation in females with autoimmune thyroid disease:: A possible explanation for the female predisposition to thyroid autoimmunity [J].
Brix, TH ;
Knudsen, GPS ;
Kristiansen, M ;
Kyvik, KO ;
Orstavik, KH ;
Hegedüs, L .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2005, 90 (11) :5949-5953
[8]   Skewed x-chromosome inactivation: Cause or consequence? [J].
Brown, CJ .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1999, 91 (04) :304-305
[9]   Association between nonrandom X-chromosome inactivation and BRCA1 mutation in germline DNA of patients with ovarian cancer [J].
Buller, RE ;
Sood, AK ;
Lallas, T ;
Buekers, T ;
Skilling, JS .
JNCI-JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1999, 91 (04) :339-346
[10]   The role of X-chromosome inactivation in female predisposition to autoimmunity [J].
Chitnis, S ;
Monteiro, J ;
Glass, D ;
Apatoff, B ;
Salmon, J ;
Concannon, P ;
Gregersen, PK .
ARTHRITIS RESEARCH, 2000, 2 (05) :399-406