Leonardson K E, Levy S B
Department of Medicine, New England Medical Center, Boston, Massachusetts.
Exp Cell Res. 1989 Jan;180(1):209-19. doi: 10.1016/0014-4827(89)90225-5.
Serial examination of five newly derived Friend murine tumors during early subcutaneous passages showed continuing changes in chromatin composition and structure over the first 10 to 20 passages followed by a period of stabilization over the subsequent 20 passages. These changes were reflected in a decrease in two major histone variants, H2A.1 and H2B.2, with a coordinate increase in histone variants, H2A.2 and H2B.1, and a changing nucleosome repeat length (NRL). The absolute values differed among the five tumors, but all five showed the same general direction of change. There was no obvious relationship among the NRL, H2A, and H2B histone variant values. A low H2A.1/H2A.2 ratio was found in Friend tumors of high malignant potential. Cell lines derived in vitro also showed directional changes in the H2A and H2B variants similar to those of their tumor cell parents, but with different kinetics. Our findings suggest that Friend tumor establishment is accompanied by an early period of chromatin reorganization marked by changes in several parameters of chromatin structure.
在早期皮下传代过程中对五个新衍生的Friend小鼠肿瘤进行的连续检查显示,在最初的10至20代中染色质组成和结构持续变化,随后在接下来的20代中出现一段稳定期。这些变化表现为两种主要组蛋白变体H2A.1和H2B.2减少,同时组蛋白变体H2A.2和H2B.1协同增加,并且核小体重复长度(NRL)发生变化。五个肿瘤的绝对值有所不同,但所有五个肿瘤都显示出相同的总体变化趋势。NRL、H2A和H2B组蛋白变体值之间没有明显关系。在具有高恶性潜能的Friend肿瘤中发现H2A.1/H2A.2比值较低。体外衍生的细胞系在H2A和H2B变体中也显示出与肿瘤细胞亲本相似的方向变化,但动力学不同。我们的研究结果表明,Friend肿瘤的形成伴随着染色质重组的早期阶段,其特征是染色质结构的几个参数发生变化。