Sheardown S A, Duthie S M, Johnston C M, Newall A E, Formstone E J, Arkell R M, Nesterova T B, Alghisi G C, Rastan S, Brockdorff N
X Inactivation Group, MRC Clinical Sciences Centre, United Kingdom.
Cell. 1997 Oct 3;91(1):99-107. doi: 10.1016/s0092-8674(01)80012-x.
The onset of X inactivation is preceded by a marked increase in the level of Xist RNA. Here we demonstrate that increased stability of Xist RNA is the primary determinant of developmental up-regulation. Unstable transcript is produced by both alleles in XX ES cells and in XX embryos prior to the onset of random X inactivation. Following differentiation, transcription of unstable RNA from the active X chromosome allele continues for a period following stabilization and accumulation of transcript on the inactive X allele. We discuss the implications of these findings in terms of models for the initiation of random and imprinted X inactivation.
X染色体失活的起始之前,Xist RNA水平会显著增加。在此我们证明,Xist RNA稳定性的增加是发育上调的主要决定因素。在随机X染色体失活开始之前,XX胚胎干细胞和XX胚胎中的两个等位基因都会产生不稳定的转录本。分化后,来自活性X染色体等位基因的不稳定RNA转录在非活性X等位基因上的转录本稳定并积累后的一段时间内仍会继续。我们根据随机和印记X染色体失活起始的模型来讨论这些发现的意义。