Xu C W, Hines J C, Engel M L, Russell D G, Ray D S
Molecular Biology Institute, University of California, Los Angeles 90095-1570, USA.
Mol Cell Biol. 1996 Feb;16(2):564-76. doi: 10.1128/MCB.16.2.564.
Kinetoplast DNA (kDNA), the mitochondrial DNA of trypanosomatids, consists of thousands of minicircles and 20 to 30 maxicircles catenated into a single large network and exists in the cell as a highly organized compact disc structure. To investigate the role of kinetoplast-associated proteins in organizing and condensing kDNA networks into this disc structure, we have cloned three genes encoding kinetoplast-associated proteins. The KAP2, KAP3, and KAP4 genes encode proteins p18, p17, and p16, respectively. These proteins are small basic proteins rich in lysine and alanine residues and contain 9-amino-acid cleavable presequences. Proteins p17 and p18 are closely related to each other, with 48% identical residues and carboxyl tails containing almost exclusively lysine, alanine, and serine or threonine residues. These proteins have been expressed as Met-His6-tagged recombinant proteins and purified by metal chelate chromatography. Each of the recombinant proteins is capable of compacting kDNA networks in vitro and was shown to bind preferentially to a specific fragment of minicircle DNA. Expression of each of these proteins in an Escherichia coli mutant lacking the HU protein rescued a defect in chromosome condensation and segregation in the mutant cells and restored a near-normal morphological appearance. Proteins p16, p17, and p18 have been localized within the cell by immunofluorescence methods and appear to be present throughout the kDNA. Electron-microscopic immunolocalization of p16 shows that p16 is present both within the kDNA disc and in the mitochondrial matrix at opposite edges of the kDNA disc. Our results suggest that nucleus-encoded H1-like proteins may be involved in the organization and segregation of kDNA networks in trypanosomatids.
动质体DNA(kDNA)是锥虫的线粒体DNA,由数千个微小环和20至30个大环连环形成一个单一的大网络,并以高度组织化的致密盘状结构存在于细胞中。为了研究与动质体相关的蛋白质在将kDNA网络组织和浓缩成这种盘状结构中的作用,我们克隆了三个编码与动质体相关蛋白质的基因。KAP2、KAP3和KAP4基因分别编码蛋白质p18、p17和p16。这些蛋白质是富含赖氨酸和丙氨酸残基的小碱性蛋白质,并含有9个氨基酸的可裂解前导序列。蛋白质p17和p18彼此密切相关,有48%的相同残基,其羧基末端几乎只包含赖氨酸、丙氨酸以及丝氨酸或苏氨酸残基。这些蛋白质已被表达为带有甲硫氨酸-组氨酸六聚体标签的重组蛋白,并通过金属螯合层析法进行纯化。每种重组蛋白都能够在体外压缩kDNA网络,并显示出优先结合微小环DNA的特定片段。在缺乏HU蛋白的大肠杆菌突变体中表达这些蛋白质中的每一种,都挽救了突变细胞中染色体浓缩和分离的缺陷,并恢复了接近正常的形态外观。通过免疫荧光方法已将蛋白质p16、p17和p18定位在细胞内,并且似乎在整个kDNA中都存在。p16的电子显微镜免疫定位显示,p16既存在于kDNA盘内,也存在于kDNA盘相对边缘的线粒体基质中。我们的结果表明,核编码的类H1蛋白可能参与锥虫中kDNA网络的组织和分离。