Banchev T, Srebreva L, Zlatanova J, Tsanev R
Institute of Molecular Biology, Bulgarian Academy of Sciences, Sofia.
Exp Cell Res. 1988 Jul;177(1):1-8. doi: 10.1016/0014-4827(88)90019-5.
By using affinity-purified antibodies to H10 and to H1AB the localization of these histones was studied by indirect immunofluorescence in the nuclei of proliferating (EAT and uninduced Friend cells) and of differentiating (induced Friend cells) cell populations. While with H1AB antibodies a bright fluorescence all over the chromatin was obtained, the localization of H10 varied depending on the state of the cell population. In the proliferating EAT cells it was localized strictly in the nucleoli. The Friend cell population revealed a heterogeneous picture with two types of H10 localization-nucleolar predominating in uninduced cell populations and peripheral predominating in induced cells. A comparison with literature data suggests that H10 seems to be associated with chromatin regions containing active genes.
通过使用针对H10和H1AB的亲和纯化抗体,采用间接免疫荧光法研究了这些组蛋白在增殖细胞群(EAT细胞和未诱导的Friend细胞)以及分化细胞群(诱导的Friend细胞)细胞核中的定位。使用H1AB抗体时,整个染色质呈现明亮荧光,而H10的定位则因细胞群状态而异。在增殖的EAT细胞中,H10严格定位于核仁。Friend细胞群呈现出异质性图像,有两种H10定位类型——在未诱导细胞群中核仁占主导,在诱导细胞中周边占主导。与文献数据比较表明,H10似乎与含有活性基因的染色质区域相关。