Bhaud Y, Géraud M L, Ausseil J, Soyer-Gobillard M O, Moreau H
Observatoire Océanologique de Banyuls, Laboratoire Arago, UMR CNRS 7628, Banyuls-sur-Mer France.
J Eukaryot Microbiol. 1999 May-Jun;46(3):259-67. doi: 10.1111/j.1550-7408.1999.tb05123.x.
Nuclei of the dinoflagellate Crypthecodinium cohnii strain Whd were isolated and nuclear proteins were extracted in three fractions, corresponding to the increasing affinity of these proteins to genomic DNA. One fraction contained two major bands (48- and 46-kDa) and antibodies specific to this fraction revealed two major bands by Western blot on nuclear extracts, corresponding to the 46- and 48-kDa bands. The 48-kDa protein was detected in G1 phase but not in M phase cells. An expression cDNA library of C. cohnii was screened with these antibodies, and two different open reading frames were isolated. Dinoflagellate nuclear associated protein (Dinap1), one of these coding sequences, was produced in E. coli and appeared to correspond to the 48-kDa nuclear protein. No homologue of this sequence was found in the data bases, but two regions were identified, one including two putative zinc finger repeats, and one coding for two potential W/W domains. The second coding sequence showed a low similarity to non-specific sterol carrier proteins. Immunocytolocalization with specific polyclonal antibodies to recombinant Dinap1 showed that the nucleus was immunoreactive only during the G1 phase: the nucleoplasm was immunostained, while chromosome cores and nuclear envelopes were negative.
对海洋双鞭毛虫寇氏隐甲藻(Crypthecodinium cohnii)菌株Whd的细胞核进行了分离,并将核蛋白提取为三个组分,这三个组分分别对应这些蛋白与基因组DNA的亲和力递增情况。其中一个组分包含两条主要条带(48 kDa和46 kDa),针对该组分的特异性抗体在对核提取物进行蛋白质免疫印迹时显示出两条主要条带,分别对应46 kDa和48 kDa的条带。48 kDa的蛋白在G1期细胞中被检测到,但在M期细胞中未被检测到。用这些抗体筛选寇氏隐甲藻的表达cDNA文库,分离出两个不同的开放阅读框。其中一个编码序列,即双鞭毛虫核相关蛋白(Dinap1),在大肠杆菌中表达,似乎对应于48 kDa的核蛋白。在数据库中未发现该序列的同源物,但鉴定出两个区域,一个区域包含两个假定的锌指重复序列,另一个区域编码两个潜在的W/W结构域。第二个编码序列与非特异性固醇载体蛋白具有较低的相似性。用针对重组Dinap1的特异性多克隆抗体进行免疫细胞定位显示,仅在G1期细胞核具有免疫反应性:核质被免疫染色,而染色体核心和核膜呈阴性。