Department of Pharmaceutical Chemistry, University of California, San Francisco, CA, USA.
mBio. 2013 May 21;4(3):e00321-13. doi: 10.1128/mBio.00321-13.
The cell membrane of a Giardia lamblia trophozoite is covered with a single species of variant-specific surface protein (VSP) that is replaced by another VSP every 6 to 13 generations of cell growth, possibly for an evasion of host immunity. Experimentally, only six VSP species have been verified to localize to the cell membrane thus far. By assuming that VSP contains multiple CXXC motifs, 219 vsp genes were annotated in GiardiaDB of the WB isolate. By further assuming that VSP possesses both CXXC motifs and a CRGKA tail at the C terminus, Adam et al. (BMC Genomics 11:424, 2010) identified a total of 303 potential vsp genes in Giardia WB. The discrepancies between these two assumed VSP identities have caused some confusion. Here, we used experimental approaches to further verify what is required of the structures of a VSP to localize to the surface of cell membrane. The data led to the following conclusions. (i) The C-terminal CRGKA sequence is not essential for localizing VSPs to the cell membrane. (ii) A "motif 1" of 45 residues, consisting of two CXXCs separated by 12 to 15 amino acid residues, located close to the C terminus and a hydrophobic "motif 2" of 38 residues at the C terminus are both essential and sufficient for localizing the protein to the cell membrane. (ii) An N-terminal sequence upstream from motif 1 is not required for targeting VSPs to the cell membrane. By these criteria, we are able to identify 73 open reading frames as the putative vsp genes in Giardia. IMPORTANCE The intestinal pathogen Giardia lamblia expresses only one variant-specific surface protein (VSP) on the cell membrane surface at a given time, but it changes spontaneously every 6 to 13 generations of growth, presumably for evading the host immunity. Only 6 VSPs have been empirically shown to localize to the cell membrane surface thus far. Here, we used mutations of VSPs and methods of identifying their locations in Giardia cells and found that a "motif 1" of 45 residues, consisting of two CXXCs separated by 12 to 15 amino acid residues, located close to the C terminus and a hydrophobic "motif 2" of 38 residues at the C terminus are the only essential and sufficient structural requirements for localizing a protein to the cell membrane. By these criteria, 73 genes are identified in the Giardia WB strain genome database as the putative repertoire of VSPs.
蓝氏贾第鞭毛虫滋养体的细胞膜覆盖着单一的变异表面蛋白 (VSP),每 6 到 13 代细胞生长就会被另一种 VSP 取代,这可能是为了逃避宿主免疫。实验表明,迄今为止,只有六种 VSP 物种被证实定位于细胞膜。通过假设 VSP 包含多个 CXXC 基序,在 WB 分离株的 GiardiaDB 中注释了 219 个 vsp 基因。通过进一步假设 VSP 具有 CXXC 基序和 C 末端的 CRGKA 尾巴,Adam 等人(BMC Genomics 11:424, 2010)在 Giardia WB 中总共鉴定了 303 个潜在的 vsp 基因。这两种假设的 VSP 身份之间的差异造成了一些混淆。在这里,我们使用实验方法进一步验证了将 VSP 定位于细胞膜表面所需的结构。这些数据得出了以下结论。(i)C 端 CRGKA 序列对于将 VSP 定位于细胞膜不是必需的。(ii)靠近 C 端的由两个 CXXC 组成的 45 个残基的“基序 1”和 C 端的 38 个残基的疏水性“基序 2”都是必需的和充分的,足以将蛋白质定位于细胞膜。(ii)位于基序 1 上游的 N 端序列不是将 VSP 靶向细胞膜所必需的。根据这些标准,我们能够鉴定出 73 个开放阅读框作为贾第虫中的推定 vsp 基因。重要性肠道病原体蓝氏贾第鞭毛虫在给定时间仅在细胞膜表面表达一种变异表面蛋白 (VSP),但它会自发地每 6 到 13 代生长就发生改变,大概是为了逃避宿主免疫。迄今为止,只有 6 种 VSP 被经验证定位于细胞膜表面。在这里,我们使用 VSP 的突变和鉴定它们在贾第虫细胞中的位置的方法,发现由两个 CXXC 组成的 45 个残基的“基序 1”,间隔 12 到 15 个氨基酸残基,靠近 C 端和 C 端的 38 个残基的疏水性“基序 2”是将蛋白质定位于细胞膜的唯一必需和充分的结构要求。根据这些标准,在 Giardia WB 菌株基因组数据库中鉴定出 73 个基因作为 VSP 的假定基因库。