Goodwin E H, Meyne J, Bailey S M, Quigley D
Los Alamos National Laboratory, Life Sciences Division, Mail Stop M888, Los Alamos, NM 87545, USA.
Chromosoma. 1996;104(5):345-7. doi: 10.1007/BF00337223.
Lateral asymmetry refers to unequal fluorescent intensity between adjacent regions of sister chromatids. It has been observed in the centromeric regions of mitotic chromosomes of mouse or human origin when cells are grown in 5-bromo-2'-deoxyuridine (BrdU) for a single round of DNA synthesis. The chromosome-orientation fluorescence in situ hybridization (CO-FISH) technique was used with pseudodiploid mouse cells to show that the regions of asymmetrical brightness coincide with major satellite repetitive DNA, and that the more heavily BrdU-substituted chromatid is the one that fluoresces less brightly. These observations support a 20 year old hypothesis on the origin of lateral asymmetry. Other observations suggest that differential loss of DNA from the heavily substituted chromatid also contributes to lateral asymmetry.
侧向不对称是指姐妹染色单体相邻区域之间荧光强度不等。当细胞在5-溴-2'-脱氧尿苷(BrdU)中生长进行一轮DNA合成时,在小鼠或人类有丝分裂染色体的着丝粒区域已观察到这种现象。染色体定向荧光原位杂交(CO-FISH)技术用于假二倍体小鼠细胞,结果表明亮度不对称的区域与主要卫星重复DNA一致,且BrdU取代程度更高的染色单体荧光亮度更低。这些观察结果支持了一个关于侧向不对称起源的已有20年历史的假说。其他观察结果表明,高度取代的染色单体DNA的差异丢失也导致了侧向不对称。