Fitzgerald P H, Morris C M
Hum Genet. 1984;67(4):385-90. doi: 10.1007/BF00291396.
About 20% of leukemic bone marrow cells from each of two patients with B-cell lymphoid leukemias showed apparent translocations which appeared to be the result of telomeric association. In one patient, whole chromosomes were associated telomere to telomere in pairs; in the other patient, telomeres of whole chromosomes were associated with breakpoints located close to the proximal or distal ends of the heterochromatic band 1q12. Repeated base sequences, particularly (CA)n sequences, are believed to be the basis of telomere pairing, and likewise repeated base sequences of heterochromatin may explain the association of 1qh and telomeres. Telomeric association may be considered as a potential origin of new stable cytogenetic combinations that have a role in oncogene transposition and tumor etiology.
两名B细胞淋巴样白血病患者的白血病骨髓细胞中,各约20%显示出明显的易位,这些易位似乎是端粒联合的结果。在一名患者中,整条染色体端粒与端粒成对联合;在另一名患者中,整条染色体的端粒与位于异染色质带1q12近端或远端附近的断点联合。重复碱基序列,尤其是(CA)n序列,被认为是端粒配对的基础,同样,异染色质的重复碱基序列可能解释1qh与端粒的联合。端粒联合可被视为新的稳定细胞遗传学组合的潜在起源,这些组合在癌基因转位和肿瘤病因学中起作用。