Glaser R L, Karpen G H, Spradling A C
Howard Hughes Medical Institute Research Laboratories, Carnegie Institution of Washington, Baltimore, MD 21210.
Chromosoma. 1992 Dec;102(1):15-9. doi: 10.1007/BF00352285.
Differential DNA replication is widely held to influence polytene chromosome structure by causing the dramatic reductions in heterochromatic DNA content that are characteristic of most endopolyploid cells. The "underreplication model" of heterochromatic sequence underrepresentation predicts that replication intermediates should populate regions of DNA between fully polytenized euchromatic sequences and underpolytenized heterochromatic sequences. We directly tested this prediction using Dp1187, a 1300 kb Drosophila minichromosome containing well-defined heterochromatic regions. DNA from a euchromatic/heterochromatic junction region of Dp1187, demonstrating a significant gradient of underrepresentation in larval salivary glands, lacked the stalled replication forks predicted by the underreplication model. We consider an alternative mechanism leading to heterochromatic sequence underrepresentation involving a process of DNA elimination.
差异DNA复制被广泛认为通过导致大多数内多倍体细胞特有的异染色质DNA含量急剧减少来影响多线染色体结构。异染色质序列代表性不足的“复制不足模型”预测,复制中间体应该存在于完全多线化的常染色质序列和多线化不足的异染色质序列之间的DNA区域。我们使用Dp1187(一个包含明确异染色质区域的1300 kb果蝇微型染色体)直接测试了这一预测。来自Dp1187常染色质/异染色质交界区域的DNA在幼虫唾液腺中表现出明显的代表性不足梯度,但缺乏复制不足模型预测的停滞复制叉。我们考虑了一种导致异染色质序列代表性不足的替代机制,该机制涉及DNA消除过程。