Staiano-Coico L, Stollar B D, Darzynkiewicz Z, Dutkowski R, Weksler M E
Mol Cell Biol. 1985 Nov;5(11):3270-3. doi: 10.1128/mcb.5.11.3270-3273.1985.
Although regions of DNA reacting with anti-Z-DNA antibodies have been identified in the polytene chromosomes of Drosophila spp. and the metaphase chromosomes from a number of different mammalian species, the biological role of this DNA is unknown. Flow cytometry was used in the present studies to quantitate the binding of anti-Z-DNA antibodies in quiescent and activated human peripheral blood lymphocytes; the antibody binding was then correlated with cell cycle phase. The data show that quiescent (G0 or G1Q) lymphocytes are heterogeneous with respect to their reaction with anti-Z-DNA antibodies. The transition from quiescence (G1Q) into the cell cycle (G1), which involves decondensation of chromatin, did not result in any significant change in binding of these antibodies. In contrast, progression of cells from G1 through S and G2 is correlated with a 27% decrease in anti-Z-DNA antibody reactivity relative to total DNA content. No significant change was observed during the transition from G2 to mitosis (M).
尽管在果蝇属的多线染色体以及多种不同哺乳动物物种的中期染色体中已鉴定出与抗Z-DNA抗体发生反应的DNA区域,但这种DNA的生物学作用尚不清楚。在本研究中,使用流式细胞术对静止和活化的人外周血淋巴细胞中抗Z-DNA抗体的结合进行定量;然后将抗体结合与细胞周期阶段相关联。数据表明,静止(G0或G1Q)淋巴细胞与抗Z-DNA抗体的反应具有异质性。从静止期(G1Q)过渡到细胞周期(G1),这涉及染色质的解聚,并未导致这些抗体的结合发生任何显著变化。相比之下,细胞从G1期经过S期和G2期的进程与抗Z-DNA抗体反应性相对于总DNA含量降低27%相关。在从G2期到有丝分裂期(M)的转变过程中未观察到显著变化。