Bittel D C, Theodoro M F, Kibiryeva N, Fischer W, Talebizadeh Z, Butler M G
Section of Medical Genetics and Molecular Medicine, Children's Mercy Hospitals and Clinics and University of Missouri - Kansas City School of Medicine, Kansas City, Missouri 64108, USA.
J Med Genet. 2008 May;45(5):309-13. doi: 10.1136/jmg.2007.055244. Epub 2007 Dec 21.
X-chromosome inactivation (XCI) is the mechanism by which gene dosage uniformity is achieved between female mammals with two X chromosomes and male mammals with a single X chromosome, and is thought to occur randomly. For molecular genetic testing, accessible tissues (eg blood) are commonly studied, but the relationship with inaccessible tissues (eg brain) is poorly understood. For accessible tissues to be informative for genetic analysis, a high degree of concordance of genetic findings among tissue types is required.
To determine the relationship among multiple tissues within females at different ages (fetus to 82 years).
XCI patterns were analysed using the polymorphic androgen receptor (AR) gene assay. DNA was isolated from 26 different human females without history of malignancy, using 34 autopsy tissues representing the three embryonic germ layers.
33 of the 280 tissue samples analysed from 13 of the 26 females showed skewed XCI values (>80:20%). Average XCI value was not significantly different among the tissues, but a trend for increasing XCI variability was observed with age in blood and other tissues studied (eg the SD for all tissues studied for the 0-2 years group was 9.9% compared with 14.8% in the >60 years group). We found a significant correlation (r(s) = 0.51, p = 0.035) between XCI values for blood and/or spleen and brain tissue, and in most other tissues representing the three embryonic germ layers.
In our study, XCI data were comparable among accessible (eg blood) and inaccessible tissues (eg brain) in females at various ages, and may be useful for genetic testing. A trend was seen for greater XCI variability with increasing age, particularly in older women (>60 years).
X染色体失活(XCI)是一种机制,通过该机制,具有两条X染色体的雌性哺乳动物与具有一条X染色体的雄性哺乳动物之间可实现基因剂量均等,并且认为其随机发生。对于分子遗传学检测,通常研究可获取的组织(如血液),但对其与不可获取组织(如脑)之间的关系了解甚少。为了使可获取组织对遗传分析具有参考价值,需要不同组织类型之间的遗传结果具有高度一致性。
确定不同年龄(从胎儿到82岁)女性体内多种组织之间的关系。
使用多态性雄激素受体(AR)基因检测分析XCI模式。从26名无恶性肿瘤病史的不同人类女性中分离DNA,使用代表三个胚胎胚层的34份尸检组织。
在26名女性中的13名所分析的280个组织样本中,有33个显示XCI值偏斜(>80:20%)。各组织之间的平均XCI值无显著差异,但在所研究的血液和其他组织中,观察到XCI变异性随年龄增加的趋势(例如,0至2岁组所有研究组织的标准差为9.9%,而>60岁组为14.8%)。我们发现血液和/或脾脏与脑组织以及代表三个胚胎胚层的大多数其他组织的XCI值之间存在显著相关性(r(s)=0.51,p=0.035)。
在我们的研究中,不同年龄女性的可获取组织(如血液)和不可获取组织(如脑)之间的XCI数据具有可比性,可能对基因检测有用。随着年龄增加,尤其是老年女性(>60岁),XCI变异性有增大的趋势。