Beletskii A, Hong Y K, Pehrson J, Egholm M, Strauss W M
Harvard Institute of Human Genetics, Beth Israel Deaconess Medical Center, Harvard Medical School, 4 Blackfan Circle, Boston, MA 02115, USA.
Proc Natl Acad Sci U S A. 2001 Jul 31;98(16):9215-20. doi: 10.1073/pnas.161173098.
The noncoding RNA Xist has been shown to be essential for X-chromosome inactivation and to coat the inactive X-chromosome (Xi). Thus, an important question in understanding the formation of Xi is whether the binding reaction of Xist is necessary for X-chromosome inactivation. In this article, we demonstrate the failure of X-chromosome silencing if the association of Xist with the X-chromosome is inhibited. The chromatin-binding region was functionally mapped and evaluated by using an approach for studying noncoding RNA function in living cells that we call peptide nucleic acid (PNA) interference mapping. In the reported experiments, a single 19-bp antisense cell-permeating PNA targeted against a particular region of Xist RNA caused the disruption of the Xi. The association of the Xi with macro-histone H2A is also disturbed by PNA interference mapping.
非编码RNA Xist已被证明对X染色体失活至关重要,并能覆盖失活的X染色体(Xi)。因此,理解Xi形成过程中的一个重要问题是Xist的结合反应对于X染色体失活是否必要。在本文中,我们证明如果Xist与X染色体的结合受到抑制,X染色体沉默就会失败。通过一种我们称为肽核酸(PNA)干扰图谱的方法来研究活细胞中非编码RNA的功能,对染色质结合区域进行了功能定位和评估。在报道的实验中,针对Xist RNA特定区域的单个19碱基对反义细胞穿透PNA导致了Xi的破坏。PNA干扰图谱也扰乱了Xi与巨核组蛋白H2A的结合。