Camargo M, Cervenka J
Am J Hum Genet. 1982 Sep;34(5):757-80.
Combining higher resolution chromosome analysis and bromodeoxyuridine (BrdU) incorporation, our study demonstrates that: (1) Human chromosomes synthesize DNA in a segmental but highly coordinated fashion. Each chromosome replicates according to its innate pattern of chromosome structure (banding). (2) R-positive bands are demonstrated as the initiation sites of DNA synthesis in all human chromosomes, including late-replicating chromosomes such as the LX and Y. (3) Replication is clearly biphasic in the sense that late-replicating elements, such as G-bands, the Yh, C-bands, and the entire LX, initiate replication after it has been completed in the autosomal R-bands (euchromatin) with minimal or no overlap. The chronological priority of R-band replication followed by G-bands is also retained in the facultative heterochromatin or late-replicating X chromosome (LX). Therefore, the inclusion of G-bands as a truly late-replicating chromatin type or G(Q)-heterochromatin is suggested. (4) Lateral asymmetry (LA) in the Y chromosome can be detected after less than half-cycle in 5-bromodeoxyuridine (BrdUrd), and the presence of at least two regions of LA in this chromosome is confirmed. (5) Finally, the replicational map of human chromosomes is presented, and a model of replication chronology is suggested. Based on this model, a system of nomenclature is proposed to place individual mitoses (or chromosomes) within S-phase, according to their pattern of replication banding. Potential applications of this methodology in clinical and theoretical cytogenetics are suggested.
结合高分辨率染色体分析和溴脱氧尿苷(BrdU)掺入技术,我们的研究表明:(1)人类染色体以片段化但高度协调的方式合成DNA。每条染色体根据其固有的染色体结构(带型)模式进行复制。(2)在所有人类染色体中,包括LX和Y等晚复制染色体,R阳性带被证明是DNA合成的起始位点。(3)复制显然是双相的,即晚复制元件,如G带、Yh、C带和整个LX,在常染色体R带(常染色质)完成复制后才开始复制,且重叠极少或没有重叠。R带复制先于G带的时间顺序在兼性异染色质或晚复制X染色体(LX)中也得以保留。因此,建议将G带归为真正的晚复制染色质类型或G(Q)异染色质。(4)在5-溴脱氧尿苷(BrdUrd)处理不到半个周期后即可检测到Y染色体的侧向不对称(LA),并证实该染色体中至少存在两个LA区域。(5)最后,展示了人类染色体的复制图谱,并提出了复制时间顺序模型。基于该模型,提出了一种命名系统,根据其复制带型模式将单个有丝分裂(或染色体)置于S期内。还提出了该方法在临床和理论细胞遗传学中的潜在应用。