Voullaire L E, Slater H R, Petrovic V, Choo K H
Murdoch Institute for Research into Birth Defects, Royal Children's Hospital, Parkville, Victoria, Australia.
Am J Hum Genet. 1993 Jun;52(6):1153-63.
We report the investigation of an unusual human supernumerary marker chromosome 10 designated "mar del(10)." This marker is present together with two other marker chromosomes in the karyotype of a boy with mild developmental delay. It has a functional centromere at a primary constriction and is mitotically stable. Fluorescence in situ hybridization (FISH) using alpha-satellite and satellite III DNA as probes failed to detect any signal at the primary constriction site. CENP-B protein could not be demonstrated, although the presence of at least some centromeric proteins was confirmed using a CREST antiserum. Consideration of these and other cytogenetic and FISH results supports a mechanism of formation of the mar del(10) chromosome involving the activation of a latent intercalary centromere at 10q25.
我们报告了对一条异常的人类额外标记染色体10(命名为“mar del(10)”)的研究。在一名轻度发育迟缓男孩的核型中,这条标记染色体与另外两条标记染色体一同存在。它在一个初级缢痕处有一个功能性着丝粒,并且在有丝分裂中是稳定的。使用α-卫星DNA和卫星III DNA作为探针进行荧光原位杂交(FISH),未能在初级缢痕位点检测到任何信号。尽管使用CREST抗血清证实至少存在一些着丝粒蛋白,但未能证明CENP-B蛋白的存在。综合这些及其他细胞遗传学和FISH结果,支持了mar del(10)染色体的形成机制,该机制涉及10q25处潜在的中间着丝粒的激活。