Barber J C K, Rodrigues R, Maloney V K, Taborda F, do C Rodrigues M, Bateman M S
Department of Human Genetics and Genomic Medicine, Faculty of Medicine, Southampton General Hospital, University of Southampton, Southampton, UK.
Cytogenet Genome Res. 2013;141(1):64-9. doi: 10.1159/000350870. Epub 2013 May 4.
Microscopically visible copy number variations within the proximal short arm heterochromatin and proximal long arm of chromosome 9 have been described as euchromatic variants (EVs) and are derived from extensive segmental duplications (SDs) that map to both the proximal short and long arms of chromosome 9. Recently, 3-4 additional copies of an SD cassette were found in 2 families with duplication EVs of 9q13-q21. Here, we report a third family with a duplication EV of 9q13-q21.1 that was ascertained at prenatal diagnosis for advanced maternal age and found in the fetus and her phenotypically normal mother. Dual-colour fluorescence in situ hybridization with bacterial artificial chromosomes RP11-246P17 and RP11-211E19 was consistent with the EV chromosome having 1-2 additional copies of a similar SD cassette, except that the SD-boundary clone RP11-88I18 was not apparently included. It is important to distinguish the 9q13-q21.1 EVs from possible pathogenic imbalances of chromosome 9, especially at prenatal diagnosis, as these EVs have no established phenotypic or reproductive consequences. The nature of the G-dark bands in 9q13-q21 EVs is briefly discussed.
在显微镜下可见的9号染色体近端短臂异染色质和近端长臂内的拷贝数变异已被描述为常染色质变异(EVs),它们源自广泛的片段重复(SDs),这些片段重复映射到9号染色体的近端短臂和长臂。最近,在2个患有9q13-q21重复EVs的家族中发现了3 - 4个额外的SD盒拷贝。在此,我们报告了第3个患有9q13-q21.1重复EVs的家族,该家族在产前诊断时因产妇年龄较大而被确定,在胎儿及其表型正常的母亲中发现。用细菌人工染色体RP11-246P17和RP11-211E19进行双色荧光原位杂交,结果与该EV染色体具有1 - 2个类似SD盒的额外拷贝一致,只是明显不包括SD边界克隆RP11-88I18。将9q13-q21.1 EVs与9号染色体可能的致病性失衡区分开来很重要,尤其是在产前诊断时,因为这些EVs没有既定的表型或生殖后果。本文简要讨论了9q13-q21 EVs中G暗带的性质。