Nash T E, Conrad J T, Mowatt M R
Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland 20892-0425, USA.
J Eukaryot Microbiol. 1995 Sep-Oct;42(5):604-9. doi: 10.1111/j.1550-7408.1995.tb05914.x.
Giardia lamblia trophozoites undergo antigenic variation by modulating the expression of variant-specific surface proteins (VSP), which are encoded by a number of small multigene families. We characterized the genomic copy of the VSP gene expressed by the cloned trophozoite line H7, derived from the isolate GS/M, in addition to a related, but nonexpressed, family member. The coding regions of the two genes encode closely related polypeptides (86% identity). However, differences in the coding region of these genes reside solely in an 873 bp segment. Only four differences were found between the 5' flanking sequences (465 bp). The proximal 205 base pairs downstream from the coding regions were identical, but thereafter the sequences diverged (37% identity over the next 391 bp). Mapping studies indicated that no other VSP gene was located within 4 kb pairs of the expressed H7 VSP gene, and transcripts from the nonexpressed gene were detected in neither GS/H7 nor heterogeneous trophozoites populations derived from this cloned line. Any mechanisms responsible for the differential expression of VSP genes must reconcile the near identity of DNA sequences that flank the coding regions of expressed and nonexpressed VSP genes.
蓝氏贾第鞭毛虫滋养体通过调节可变特异性表面蛋白(VSP)的表达来进行抗原变异,这些蛋白由多个小多基因家族编码。我们对克隆的滋养体系H7(源自分离株GS/M)所表达的VSP基因的基因组拷贝进行了表征,此外还研究了一个相关但不表达的家族成员。这两个基因的编码区编码密切相关的多肽(同一性为86%)。然而,这些基因编码区的差异仅存在于一个873 bp的片段中。在5'侧翼序列(465 bp)之间仅发现四个差异。编码区下游近端的205个碱基对是相同的,但此后序列发生分歧(在接下来的391 bp中同一性为37%)。图谱研究表明,在表达的H7 VSP基因的4 kb对范围内没有其他VSP基因,并且在GS/H7或源自该克隆系的异质滋养体群体中均未检测到来自未表达基因的转录本。负责VSP基因差异表达的任何机制都必须协调已表达和未表达VSP基因编码区侧翼DNA序列的近乎同一性。