Marella Narasimharao V, Zeitz Michael J, Malyavantham Kishore S, Pliss Artem, Matsui Sei-ichi, Goetze Sandra, Bode Juergen, Raska Ivan, Berezney Ronald
Department of Biological Sciences, University at Buffalo, State University of New York, Buffalo, NY 14260, USA.
Chromosome Res. 2008;16(8):1177-92. doi: 10.1007/s10577-008-1267-x. Epub 2008 Nov 15.
The organization of the type I interferon (IFN) gene cluster (9p21.3) was studied in a human osteosarcoma cell line (MG63). Array comparative genomic hybridization (aCGH) showed an amplification of approximately 6-fold which ended at both ends of the gene cluster with a deletion that extended throughout the 9p21.3 band. Spectral karyotyping (SKY) combined with fluorescence in-situ hybridization (FISH) identified an arrangement of the gene cluster in a ladder-like array of 5-7 'bands' spanning a single chromosome termed the 'IFN chromosome'. Chromosome painting revealed that the IFN chromosome is derived from components of chromosomes 4, 8 and 9. Labelling with centromeric probes demonstrated a ladder-like amplification of centromeric 4 and 9 sequences that co-localized with each other and a similar banding pattern of chromosome 4, as well as alternating with the IFN gene clusters. In contrast, centromere 8 was not detected on the IFN chromosome. One of the amplified centromeric 9 bands was identified as the functional centromere based on its location at the chromosome constriction and immunolocalization of the CENP-C protein. A model is presented for the generation of the IFN chromosome that involves breakage-fusion-bridge events.
在人骨肉瘤细胞系(MG63)中研究了I型干扰素(IFN)基因簇(9p21.3)的组织情况。阵列比较基因组杂交(aCGH)显示约6倍的扩增,该扩增在基因簇的两端终止,同时存在贯穿9p21.3带的缺失。光谱核型分析(SKY)结合荧光原位杂交(FISH)确定基因簇以一种阶梯状阵列排列,该阵列跨越一条称为“IFN染色体”的单一染色体,包含5 - 7个“带”。染色体涂染显示IFN染色体源自4号、8号和9号染色体的成分。用着丝粒探针标记显示着丝粒4和9的序列呈阶梯状扩增,它们相互共定位,4号染色体具有相似的带型模式,并且与IFN基因簇交替出现。相比之下,在IFN染色体上未检测到8号着丝粒。基于其位于染色体缢缩处以及CENP - C蛋白的免疫定位,其中一个扩增的9号着丝粒带被确定为功能着丝粒。提出了一个涉及断裂 - 融合 - 桥事件的IFN染色体生成模型。