The mouse Smcx gene exhibits developmental and tissue specific variation in degree of escape from X inactivation

被引:46
作者
Sheardown, S
Norris, D
Fisher, A
Brockdorff, N
机构
[1] HAMMERSMITH HOSP, ROYAL POSTGRAD MED SCH,MRC,CTR CLIN SCI, COMPARAT BIOL GRP, LONDON W12 0NN, ENGLAND
[2] HAMMERSMITH HOSP, ROYAL POSTGRAD MED SCH,MRC,CTR CLIN SCI, LYMPHOCYTE DEV GRP, LONDON W12 0NN, ENGLAND
基金
英国医学研究理事会;
关键词
D O I
10.1093/hmg/5.9.1355
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 Smcx gene is the first known example of a non-pseudoautosomal X-linked gene in mouse that normally escapes X chromosome inactivation. We have analysed the kinetics of escape at different stages of development, and in adult tissues. Our results demonstrate that Smcx exhibits partial escape from X inactivation in embryos, in extraembryonic lineages where paternally imprinted X inactivation occurs and also in adult tissues. The degree of escape in different tissues is highly variable, the level of transcript from the inactive X allele representing between 20% and 70% of the active X allele. Partial escape is also seen in clones derived from haematopoietic stem cells, suggesting that partial repression of the inactive X allele is at the level of individual cells. This contrasts with classical position effect variegation (PEV), where a given gene is either active or silent in a given cell and its clonal derivatives, We discuss the implications of these results with respect to mechanisms of X inactivation and escape.
引用
收藏
页码:1355 / 1360
页数:6
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