Van Dyke D L, Flejter W L, Worsham M J, Roberson J R, Higgins J V, Herr H M, Knuutila S, Wang N, Babu V R, Weiss L
Am J Hum Genet. 1986 Jul;39(1):88-95.
It is paradoxical that the inactivated X is the only chromosome that can be identified in the interphase nucleus, yet in metaphase, it is indistinguishable from its genetically active homolog unless special culture and staining procedures are employed. A specific inactivation-associated fold in proximal Xq resolves that paradox. We describe here how the fold in the proximal long arm can be used as a simple and reliable marker to identify the inactivated X in G-, Q-, or R-banded preparations. Several examples are given, including localization of the inactivation center to band Xq13 or q21.1, identification of nonrandom inactivation in X-chromosome rearrangements, identification of multiple active X chromosomes in tumor cell lines, analysis of X-inactivation patterns in female carriers of the fragile site at Xq27, and comparison of X-inactivation patterns among primate species.
矛盾的是,失活的X染色体是唯一在间期核中可被识别的染色体,但在中期,除非采用特殊的培养和染色程序,否则它与其具有遗传活性的同源染色体无法区分。近端Xq中特定的失活相关折叠解决了这一矛盾。我们在此描述近端长臂中的这种折叠如何能够用作一种简单可靠的标记,以在G带、Q带或R带制备物中识别失活的X染色体。给出了几个例子,包括将失活中心定位到Xq13或q21.1带、识别X染色体重排中的非随机失活、识别肿瘤细胞系中的多个活性X染色体、分析Xq27处脆性位点女性携带者的X失活模式以及比较灵长类物种之间的X失活模式。