Wolff D J, Brown C J, Schwartz S, Duncan A M, Surti U, Willard H F
Department of Genetics and Center for Human Genetics, Case Western Reserve University, Cleveland, OH 44106.
Am J Hum Genet. 1994 Jul;55(1):87-95.
The abnormal phenotype and/or mental retardation seen in persons with small marker X (mar(X)) chromosomes has been hypothesized to be due to the loss of the X inactivation center (XIC) at Xq13.2, resulting in two active copies of genes in the pericentromeric region. In order to define precisely the DNA content of mar(X) chromosomes and to correlate phenotype with karyotype, we studied small mar(X) chromosomes, using FISH with probes in the juxtacentromeric region. One of the probes was a 40-kb genomic cosmid for the XIST gene, which maps to the smallest interval known to contain the XIC and is thought to be involved in X inactivation. Our findings reveal that small mar(X) chromosomes do not include the XIC and therefore cannot be subject to X inactivation, supporting the premise that abnormal dosage of expressed genes in the pericentromeric region of the X generates the aberrant phenotype seen in patients with small mar(X) chromosomes.
小标记X(mar(X))染色体患者中出现的异常表型和/或智力迟钝被推测是由于Xq13.2处X失活中心(XIC)的缺失,导致着丝粒周围区域的基因有两个活性拷贝。为了精确界定mar(X)染色体的DNA含量,并将表型与核型相关联,我们使用近着丝粒区域的探针进行荧光原位杂交(FISH),研究了小mar(X)染色体。其中一个探针是针对XIST基因的40 kb基因组黏粒,该基因定位于已知包含XIC的最小区间,并且被认为参与X失活。我们的研究结果表明,小mar(X)染色体不包含XIC,因此不能进行X失活,这支持了以下前提:X着丝粒周围区域中表达基因的剂量异常会导致小mar(X)染色体患者出现异常表型。