Spittel Hannes, Kubek Florian, Kreskowski Katharina, Ziegler Monika, Klein Elisabeth, Hamid Ahmed B, Kosyakova Nadezda, Radhakrishnan Gopakumar, Junge Annelore, Kozlowski Peter, Schulze Berndt, Martin Thomas, Huhle Dagmar, Mehnert Karl, Rodríguez Laura, Ergun Mehmet A, Sarri Catherine, Militaru Mariela, Stipoljev Fedora, Tittelbach Hanne, Vasheghani Faezeh, de Bello Cioffi Marcelo, Hussein Shaymaa S, Fan Xiaobo, Volleth Marianne, Liehr Thomas
Institute of Human Genetics, Jena University Hospital, Friedrich Schiller University, Jena, Germany.
Cytogenet Genome Res. 2014;142(3):151-60. doi: 10.1159/000360776. Epub 2014 Apr 1.
Small supernumerary marker chromosomes (sSMC) are known for being present in mosaic form as 47,+mar/46 in >50% of the cases with this kind of extra chromosomes. However, no detailed studies have been done for the mitotic stability of sSMC so far, mainly due to the lack of a corresponding in vitro model system. Recently, we established an sSMC-cell bank (Else Kröner-Fresenius-sSMC-cellbank) with >150 cell lines. Therefore, 93 selected sSMC cases were studied here for the presence of the corresponding marker chromosomes before and after Epstein-Barr virus-induced immortalization. The obtained results showed that dicentric inverted duplicated-shaped sSMC are by far more stable in vitro than monocentric centric minute- or ring-shaped sSMC. Simultaneously, a review of the literature revealed that a comparable shape-dependent mitotic stability can be found in vivo in sSMC carriers. Additionally, a possible impact of the age of the sSMC carrier on mitotic stability was found: sSMC cell lines established from patients between 10-20 years of age were predominantly mitotically unstable. The latter finding was independent of the sSMC shape. The present study shows that in vitro models can lead to new and exciting insights into the biology of this genetically and clinically heterogeneous patient group.
小额外标记染色体(sSMC)在超过50%的此类额外染色体病例中以47,+mar/46的嵌合形式存在。然而,迄今为止,尚未对sSMC的有丝分裂稳定性进行详细研究,主要原因是缺乏相应的体外模型系统。最近,我们建立了一个包含150多个细胞系的sSMC细胞库(Else Kröner - Fresenius - sSMC细胞库)。因此,在此研究了93例选定的sSMC病例,观察在爱泼斯坦 - 巴尔病毒诱导永生化前后相应标记染色体的存在情况。所得结果表明,双着丝粒倒位重复形sSMC在体外远比单着丝粒中心微小形或环形sSMC稳定。同时,文献综述显示,在sSMC携带者体内也能发现类似的形状依赖性有丝分裂稳定性。此外,还发现了sSMC携带者年龄对有丝分裂稳定性可能产生的影响:从10至20岁患者中建立的sSMC细胞系主要有丝分裂不稳定。后一发现与sSMC形状无关。本研究表明,体外模型能够为这个遗传和临床异质性患者群体的生物学特性带来新的、令人兴奋的见解。