Capozzi Oronzo, Purgato Stefania, Verdun di Cantogno Ludovica, Grosso Enrico, Ciccone Roberto, Zuffardi Orsetta, Della Valle Giuliano, Rocchi Mariano
Department of Genetics and Microbiology, University of Bari, Bari, Italy.
Chromosoma. 2008 Aug;117(4):339-44. doi: 10.1007/s00412-008-0150-z. Epub 2008 Feb 15.
It has been hypothesized that human clinical neocentromeres and evolutionary novel centromeres (ENC) represent two faces of the same phenomenon. However, there are only two reports of loci harboring both a novel centromere and a clinical neocentromere. We suggest that only the tip of the iceberg has been scratched because most neocentromerization events have a very low chance of being observed. In support of this view, we report here on a neocentromere at 9q33.1 that emerged in a ring chromosome of about 12 Mb. The ring was produced by a balanced rearrangement that was fortuitously discovered because of its malsegregation in the propositus. Chromatin-immunoprecipitation-on-chip experiments using anti-centromere protein (CENP)-A and anti-CENP-C antibodies strongly indicated that a novel centromeric domain was present in the ring, in a chromosomal domain where an ENC emerged in the ancestor to Old World monkeys.
据推测,人类临床新着丝粒和进化上的新型着丝粒(ENC)代表了同一现象的两个方面。然而,仅有两份关于同时含有新型着丝粒和临床新着丝粒位点的报告。我们认为目前所了解的只是冰山一角,因为大多数新着丝粒形成事件被观察到的可能性非常低。为支持这一观点,我们在此报告一个位于9q33.1的新着丝粒,它出现在一条约12 Mb的环状染色体上。该环是由一次平衡重排产生的,由于其在先证者中发生错误分离而被偶然发现。使用抗着丝粒蛋白(CENP)-A和抗CENP-C抗体进行的芯片染色质免疫沉淀实验有力地表明,在该环中存在一个新型着丝粒结构域,该结构域位于旧世界猴祖先中出现ENC的染色体区域。