Regulation of X-Inactivation by Non-Coding RNA Loci

哺乳动物在雌性发育早期通过转录沉默一条X染色体来实现剂量补偿。X染色体失活(XCI)是由X染色体失活中心控制的，X染色体失活中心是控制X染色体计数、选择和沉默的必要和充分的顺式作用中心。我们的长期目标是了解每一步的分子基础。目前已知的是，X失活中心的非编码产物Xist RNA“绘制”了失活的X，并需要启动该X的全局沉默。从上一个资助期开始的工作导致在X失活中心发现了两个新的非编码RNA基因座。Xist是Xist的反义基因，它抑制Xist的表达，并指定未来活跃的Xist。Xite是一个与低水平基因间转录本相关的基因，它正向调节TSix的表达。因此，X失活中心的所有已知调控元件都会产生非编码RNA。这项拟议的研究将剖析TSix和Xite的作用机制。具体地说，拟议的研究将(1)确定Xite和tSix如何抑制Xist RNA的传播，(2)定义X失活印记和选择的分子基础，以及(3)测试Xite是否是Xce(“X控制元件”)，Xce是XCI等位基因比率的长期难以捉摸的修饰物，它与X连锁疾病女性携带者XCI的不利偏斜有关。作为哺乳动物中为数不多的反义基因之一，tSix是反义调控的范例。作为哺乳动物中仅有的两个功能性基因间转录元件之一，Xite将对这一新出现的基因间现象有一个有限的了解。从研究计划中获得的信息也将对人类遗传学、癌症和动物克隆以及染色体、染色质结构和转录调控的基本生物学产生重大影响。

Mammals achieve dosage compensation by transcriptional silencing of one X-chromosome in early female development. X-chromosome inactivation (XCI) is controlled by a master locus known as the "X-inactivation center," a cis-acting center which is both necessary and sufficient to direct X-chromosome counting, choice, and initiation of silencing. Our long term goal is to understand the molecular underpinnings of each step. It is currently known that Xist RNA, a non-coding product of the X-inactivation center, "paints" the inactive X and is required to initiate global silencing of that X. Work from the last funding period led to the discovery of two novel non-coding RNA loci at the X-inactivation center. Tsix, a gene antisense to Xist, inhibits Xist expression and designates the future active X. Xite, a locus associated with low-level intergenic transcripts, positively regulates Tsix expression. Thus, all known regulatory elements at the X-inactivation center make non-coding RNA. The proposed research will dissect the mechanism of action by Tsix and Xite. Specifically, the proposed research will (1) determine how Xite and Tsix inhibit the spread of Xist RNA, (2) define the molecular basis of X-inactivation imprinting and choice, and (3) test if Xite is the Xce ("X-controlling element"), the long-elusive modifier of XCI allele ratios which has been implicated in unfavorable skewing of XCI in female carriers of X-linked disease. As one of very few antisense loci in mammals, Tsix serves as a paradigm for antisense regulation. As one of only two known functional intergenic transcription elements in mammals, Xite will advance a limited knowledge of this emerging intergenic phenomenon. Information gained from the research program will also have significant impact on human genetics, cancer, and animal cloning, as well as on the basic biology of chromosomes, chromatin structure, and transcriptional regulation.