Stahl H D, Crewther P E, Anders R F, Kemp D J
Walter and Eliza Hall Institute of Medical Research, Victoria, Australia.
Mol Biol Med. 1987 Aug;4(4):199-211.
The falciparum interspersed repeat antigen (FIRA) plays a dominant role in the human antibody response to the malaria parasite Plasmodium falciparum. We have therefore determined the complete sequence of a genomic clone encoding FIRA. The FIRA gene contains a single intervening sequence, located immediately 3' to the putative hydrophobic core of a signal sequence in the short (100 amino acids) exon 1. The second exon largely encodes blocks of 13 hexapeptide repeats based loosely on the consensus sequence Pro-Val-Thr-Thr-Gln-Glu. The first block encoded 39 hexapeptides followed by about nine blocks of 13 hexapeptides interspersed between a conserved region of 81 amino acids, which is itself repeated along the molecule. Although deletions of repeats in this and four other independent clones make the exact number of blocks uncertain, this structure is supported by genomic blotting studies. As 31 variants of the repeat have been identified so far, we suggest that this extreme repeat variability must have important implications for the host immune response.
恶性疟原虫散布重复抗原(FIRA)在人类针对疟原虫恶性疟原虫的抗体反应中起主导作用。因此,我们已经确定了编码FIRA的基因组克隆的完整序列。FIRA基因包含一个单一的间隔序列,位于短(100个氨基酸)外显子1中信号序列推定的疏水核心的紧挨着的3'端。第二个外显子主要编码基于一致序列Pro-Val-Thr-Thr-Gln-Glu松散排列的13个六肽重复序列块。第一个块编码39个六肽,随后是大约九个13个六肽的块,散布在一个81个氨基酸的保守区域之间,该保守区域本身沿分子重复。尽管这个克隆和其他四个独立克隆中重复序列的缺失使得块的确切数量不确定,但这种结构得到了基因组印迹研究的支持。由于到目前为止已经鉴定出31种重复序列变体,我们认为这种极端的重复序列变异性必定对宿主免疫反应具有重要影响。