Howe L, Itoh T, Katagiri C, Ausió J
Department of Biochemistry and Microbiology, University of Victoria, B.C., Canada.
Biochemistry. 1998 May 19;37(20):7077-82. doi: 10.1021/bi980410o.
It has long been proposed that selective binding of histone H1 is, in part, responsible for the differential developmental regulation of the oocyte and somatic 5S rRNA genes in Xenopus laevis. In this study we show that histone H1 binds both oocyte and somatic genes equally after reconstitution into mononucleosomes or oligonucleosome arrays. Furthermore, we show that the binding of histone H1 selectively represses only oocyte gene transcription and that an RNA polymerase III transcription complex is able to initiate transcription of nucleosomal somatic templates regardless of whether histone H1 is present. These results support a model in which the differential regulation of the 5S rRNA genes is not simply due to the prevention of histone H1 binding by transcription complexes on the somatic genes, but rather to a difference in the histone H1 interaction with the somatic and oocyte genes.
长期以来,人们一直认为组蛋白H1的选择性结合在一定程度上导致了非洲爪蟾卵母细胞和体细胞5S rRNA基因的差异发育调控。在本研究中,我们发现,在重构为单核小体或寡核小体阵列后,组蛋白H1与卵母细胞基因和体细胞基因的结合能力相同。此外,我们还发现,组蛋白H1的结合仅选择性地抑制卵母细胞基因的转录,并且无论组蛋白H1是否存在,RNA聚合酶III转录复合物都能够起始核小体体细胞模板的转录。这些结果支持了这样一种模型,即5S rRNA基因的差异调控并非简单地由于转录复合物对体细胞基因上组蛋白H1结合的阻止,而是由于组蛋白H1与体细胞基因和卵母细胞基因相互作用的差异。