Popova Bilyana C, Tada Takashi, Takagi Nobuo, Brockdorff Neil, Nesterova Tatyana B
Developmental Epigenetics, Medical Research Council Clinical Sciences Center, Imperial College Faculty of Medicine, Hammersmith Hospital, DuCane Road, London W12 ONN, United Kingdom.
Proc Natl Acad Sci U S A. 2006 May 16;103(20):7706-11. doi: 10.1073/pnas.0602021103. Epub 2006 May 5.
X inactivation in female mammals involves transcriptional silencing of an entire chromosome in response to a cis-acting noncoding RNA, the X inactive-specific transcript (Xist). Xist can also inactivate autosomal sequences, for example, in X;autosome translocations; but here, silencing appears to be relatively inefficient. This variation has been attributed to either attenuated spreading of Xist RNA at the onset of X inactivation or inefficient maintenance of autosomal silencing. Evidence to date has favored the latter. Here, we demonstrate attenuated spreading of Xist RNA at the onset of X inactivation in the T(X;4)37H X;autosome translocation. Our findings provide direct evidence that underlying chromosome/chromatin features can disrupt spreading of the primary inactivating signal.
雌性哺乳动物中的X染色体失活涉及整条染色体的转录沉默,这是对一种顺式作用非编码RNA——X染色体失活特异性转录本(Xist)的响应。Xist也能使常染色体序列失活,例如在X;常染色体易位中;但在此情况下,沉默似乎相对低效。这种差异被归因于X染色体失活开始时Xist RNA的扩散减弱或常染色体沉默的维持效率低下。迄今为止的证据支持后者。在这里,我们证明了在T(X;4)37H X;常染色体易位中,X染色体失活开始时Xist RNA的扩散减弱。我们的发现提供了直接证据,表明潜在的染色体/染色质特征可破坏初级失活信号的扩散。