Heard E, Avner P, Rothstein R
Unité de Génétique Moléculaire Murine, CNRS URA 1445, Institut Pasteur, Paris, France.
Nucleic Acids Res. 1994 May 25;22(10):1830-7. doi: 10.1093/nar/22.10.1830.
Two mouse YACs, PA-2 and PA-3, contain the Xist gene and are 460 kb and 3.3 Mb long respectively. While PA-2 is non-chimeric, PA-3 contains a substantial proportion of non-contiguous DNA. As a prerequisite to functional studies of the role of this region in X inactivation, we have created a deletion series of YACs that are spaced at approximately 50 kb intervals and were able to eliminate the unwanted chimeric sequences in YAC PA-3. For this purpose, we have constructed mouse B1 fragmentation vectors based on those described for human Alu fragmentation. Having created this series of YAC deletion derivatives, we were able to eliminate efficiently the 10-15% aberrant YACs that arise during the course of a fragmentation experiment by assessing their marker content. The overlap and the opposite orientation of the two YAC inserts permitted the creation of deletions on both sides of the 500 kb region around Xist. The use of this series of YACs in a biological assay will help us define the extent of the sequences necessary to bring about X chromosome inactivation.
两个小鼠YAC(PA - 2和PA - 3)包含Xist基因,长度分别为460 kb和3.3 Mb。PA - 2是非嵌合的,而PA - 3包含相当比例的非连续DNA。作为研究该区域在X染色体失活中作用的功能研究的前提,我们构建了一系列YAC缺失体,间隔约50 kb,并且能够消除YAC PA - 3中不需要的嵌合序列。为此,我们基于用于人类Alu片段化的载体构建了小鼠B1片段化载体。构建了这一系列YAC缺失衍生物后,通过评估其标记物含量,我们能够有效消除在片段化实验过程中出现的10% - 15%的异常YAC。两个YAC插入片段的重叠和相反方向允许在Xist周围500 kb区域的两侧产生缺失。在生物学分析中使用这一系列YAC将有助于我们确定导致X染色体失活所需序列的范围。