Liang Desheng, Wu Lingqian, Pan Qian, Harada Naoki, Long Zhigao, Xia Kun, Yoshiura Koh-Ichiro, Dai Heping, Niikawa Norio, Cai Fang, Xia Jiahui
National Laboratory of Medical Genetics of China, Xiangya Hospital, Central South University, Changsha, China.
Am J Med Genet A. 2006 Feb 1;140(3):238-44. doi: 10.1002/ajmg.a.31077.
A male patient with mental retardation (MR) and mild facial features was shown by high-resolution G-banding to have pericentric inversion of chromosome 12 with an unknown segment inserted into the long arm of the inverted chromosome [46,XY,inv(12)(pter-->p11.2::q14.1-->p11.2::?::q14.1-->qter)]. Both the inverted chromosome 12 and clinical manifestations were transmitted to his son. Karyotypes of the propositus' parents were normal. Studies with fluorescence in situ hybridization (FISH) in both the propositus and his son revealed that the extra segment was derived from 12p. Further FISH mapping and the genome-wide copy number detection by GeneChip Mapping 100K Array showed that an 11-Mb segment of 12p between two BAC clones, RP11-22H10 and RP11-977P2, was inserted at one of the reunion points in the long arm of the inv(12) chromosome. Analysis of parent-child transmissions of duplicated alleles using microsatellite markers defined the maternal origin of the chromosomal anomaly in the propositus and suggested a mechanism of its formation through a sister-chromatid rearrangement (SCR), that is, mismatched pairing and unequal crossover between sister chromatids as well as three break rearrangements including a U type rearrangement. Karyotypes of the propositus and his son were thus inv(12)(pter-->p11.22::q14.1-->p12.3::q14.1-->qter). This is the first report of "pure" proximal 12p-trisomy including p12.3-p11.22 region.
一名患有智力迟钝(MR)且面部特征轻微的男性患者,经高分辨率G显带分析显示,其12号染色体发生了臂间倒位,一条未知片段插入到了倒位染色体的长臂中[46,XY,inv(12)(pter→p11.2::q14.1→p11.2::?::q14.1→qter)]。倒位的12号染色体及临床表现均遗传给了他的儿子。先证者父母的核型正常。对先证者及其儿子进行荧光原位杂交(FISH)研究发现,额外片段源自12p。进一步的FISH定位以及通过基因芯片Mapping 100K Array进行的全基因组拷贝数检测表明,在两个BAC克隆RP11-22H10和RP11-977P2之间的12p上一个11-Mb的片段插入到了inv(12)染色体长臂的一个重聚点处。使用微卫星标记对重复等位基因的亲子传递进行分析,确定了先证者染色体异常的母系起源,并提示其形成机制为姐妹染色单体重排(SCR),即姐妹染色单体之间错配配对和不等交换以及包括U型重排在内的三次断裂重排。因此,先证者及其儿子的核型为inv(12)(pter→p11.22::q14.1→p12.3::q14.1→qter)。这是关于包括p12.3 - p11.22区域的“纯”近端12p三体的首次报道。