Yanagi Akira
Department of Biotechnology, Senshu University of Ishinomaki, Ishinomaki 986, Japan.
Dev Growth Differ. 1992 Dec;34(6):613-618. doi: 10.1111/j.1440-169X.1992.tb00029.x.
To know molecular mechanism controlling the differentiation of somatic nuclei (macronuclei) in Paramecium caudatum, I obtained the monoclonal antibody 36B against a macronuclear antigen. Immunocytochemical observations showed that the antigen 36B was dispersed in macronuclei. But in late stationary phase, large aggregation of the antigen was observed in some stocks, though this was not observed in another stock. In addition, the 36B-positive portion in macronuclei seemed to contain smaller amount of DNA than the remaining portion. These observations suggest that the antigen 36B exists in nucleoli in the macronucleus. In the late stage of conjugation, the antigen 36B was retained in the degenerating fragments derived from old macronuclei as long as the fragments persisted. In the beginning of the development of new macronuclei, the antigen 36B was not observed in four macronuclear anlagen, but after a while it appeared in all of them. This shows that the macronuclear anlagen newly get the antigen 36B during their development. Since the appearance of the antigen 36B coincides with the stage when macronuclei are known to be transcriptionally active, the antigen 36B may be involved in the expression of genes in macronuclei. This is consistent with the possibility that the antigen 36B may be a component of nucleoli.
为了解控制尾草履虫体细胞核(大核)分化的分子机制,我获得了一种针对大核抗原的单克隆抗体36B。免疫细胞化学观察表明,抗原36B分散在大核中。但在静止后期,在一些品系中观察到该抗原大量聚集,不过在另一个品系中未观察到这种现象。此外,大核中36B阳性部分的DNA含量似乎比其余部分少。这些观察结果表明,抗原36B存在于大核的核仁中。在接合后期,只要旧大核衍生的退化片段持续存在,抗原36B就会保留在这些片段中。在新大核发育初期,在四个大核原基中未观察到抗原36B,但过了一段时间后,在所有大核原基中都出现了。这表明大核原基在发育过程中重新获得了抗原36B。由于抗原36B的出现与已知大核转录活跃的阶段一致,抗原36B可能参与大核中的基因表达。这与抗原36B可能是核仁成分的可能性相符。