Fletcher Terace M
University of Miami School of Medicine, Department of Biochemistry and Molecular Biology, 1011 NW 15 Street, Rm. 210 (R629), Miami, FL 33136, USA.
IUBMB Life. 2003 Aug;55(8):443-9. doi: 10.1080/15216540310001612228.
Telomeres, nucleoprotein complexes at the end of eukaryotic chromosomes, have vital roles in chromosome integrity. Telomere chromatin structure is both intricate and dynamic allowing for a variety of responses to several stimuli. A critical determinant in telomere structure is the G-strand overhang. Facilitated by telomeric proteins, the G-strand overhang stabilizes telomere higher-order assemblies most likely by adopting unusual DNA structures. These structures influence activities that occur at the chromosome end. Dysfunctional telomeres induce signals resulting in cell growth arrest or death. To overcome telomere dysfunction, cancer cells activate the DNA polymerase, telomerase. The presence of telomerase at the telomere may establish a particular telomeric state. If the chromosome ends of cancer and normal cells exist in different states, cancer-specific telomere structures would offer a unique chemotherapeutic target.
端粒是真核染色体末端的核蛋白复合体,在染色体完整性方面发挥着至关重要的作用。端粒染色质结构既复杂又动态,能够对多种刺激产生多种反应。端粒结构的一个关键决定因素是G链悬突。在端粒蛋白的促进下,G链悬突很可能通过采用异常的DNA结构来稳定端粒高阶组装体。这些结构影响着发生在染色体末端的活动。功能失调的端粒会引发信号,导致细胞生长停滞或死亡。为了克服端粒功能障碍,癌细胞会激活DNA聚合酶端粒酶。端粒酶在端粒处的存在可能会建立一种特定的端粒状态。如果癌细胞和正常细胞的染色体末端处于不同状态,癌症特异性的端粒结构将提供一个独特的化疗靶点。