Bobek L A, LoVerde P T, Rekosh D M
Department of Microbiology, State University of New York at Buffalo 14214.
Exp Parasitol. 1989 Jan;68(1):17-30. doi: 10.1016/0014-4894(89)90004-0.
Eggshell protein genes of Schistosoma mansoni that encode a 14 kDa protein have been shown to be highly conserved and expressed in a sex-, tissue-, and temporal-specific manner. To initiate studies on the eggshell protein genes of S. haematobium, a cDNA probe, pSMf 61-46, representing a S. mansoni eggshell protein mRNA was used to screen a S. haematobium genomic library. Of the seven independent recombinant clones isolated, two (lambda SH 2-1 and lambda SH 6-1) were analyzed and compared to those of S. mansoni. lambda SH 2-1 and lambda SH 6-1 each contain a different genomic copy of the gene encoding a 19.8 and 17.6 kDa protein, respectively. This is due to an additional 78 bp present in the coding region of lambda SH 2-1 relative to lambda SH 6-1. The rest of the coding sequences are identical, and the 5' and 3' untranslated regions are nearly identical. The deduced amino acid sequences of S. haematobium eggshell proteins are very rich in glycine (47 and 50%) when compared to 43.5% glycine in the protein encoded by S. mansoni. Long stretches of glycines, as many as 15 in a row, occur in the S. haematobium sequence. DNA comparison of the eggshell protein genes of the two schistosome species yielded an overall homology of 83.1%. The homology is much higher in the 5' and 3' untranslated regions than in the protein-coding regions. Genomic clones of both species contained second open reading frames, which appeared to be kept open as a consequence of the amino acid composition of the other. There are no introns in S. haematobium or S. mansoni eggshell protein genes, and the genomic Southern data indicated a similar arrangement of these genes in the genome of both species. Primer extension experiments and dideoxynucleotide sequencing of the RNA determined the mRNA cap site sequence as ATCAT and ATCAC in lambda SH 2-1 and lambda SH 6-1, respectively. Northern blot analysis determined the size of the mRNA to be about 1.0 kp. Expression of the RNA from these genes appears to be regulated in a manner similar to the corresponding genes in S. mansoni. mRNA is found only in mature females and first appears at 70 days after infection of hamsters. DNA sequence comparisons of the 5' flanking regions of S. haematobium and S. mansoni eggshell protein genes to each other and to those of silkmoth and Drosophila revealed several short sequence elements that are shared.(ABSTRACT TRUNCATED AT 400 WORDS)
编码一种14 kDa蛋白的曼氏血吸虫卵壳蛋白基因已被证明高度保守,并以性别、组织和时间特异性的方式表达。为了启动对埃及血吸虫卵壳蛋白基因的研究,使用代表曼氏血吸虫卵壳蛋白mRNA的cDNA探针pSMf 61 - 46筛选埃及血吸虫基因组文库。在分离出的7个独立重组克隆中,分析了其中2个(λSH 2 - 1和λSH 6 - 1)并与曼氏血吸虫的克隆进行比较。λSH 2 - 1和λSH 6 - 1分别包含编码19.8 kDa和17.6 kDa蛋白的基因的不同基因组拷贝。这是因为相对于λSH 6 - 1,λSH 2 - 1的编码区存在额外的78 bp。其余编码序列相同,5'和3'非翻译区几乎相同。与曼氏血吸虫编码的蛋白中43.5%的甘氨酸相比,埃及血吸虫卵壳蛋白的推导氨基酸序列富含甘氨酸(分别为47%和50%)。在埃及血吸虫序列中出现了长达15个连续的甘氨酸长片段。两种血吸虫卵壳蛋白基因的DNA比较显示总体同源性为83.1%。5'和3'非翻译区的同源性比蛋白编码区高得多。两个物种的基因组克隆都包含第二个开放阅读框,由于另一个的氨基酸组成,这些开放阅读框似乎保持开放状态。埃及血吸虫和曼氏血吸虫卵壳蛋白基因中没有内含子,基因组Southern数据表明这两个物种基因组中这些基因的排列相似。引物延伸实验和RNA的双脱氧核苷酸测序确定λSH 2 - 1和λSH 6 - 1中mRNA帽位点序列分别为ATCAT和ATCAC。Northern印迹分析确定mRNA大小约为1.0 kp。这些基因的RNA表达调控方式似乎与曼氏血吸虫中的相应基因相似。mRNA仅在成熟雌性中发现,并且在仓鼠感染后70天首次出现。埃及血吸虫和曼氏血吸虫卵壳蛋白基因5'侧翼区彼此之间以及与家蚕和果蝇的5'侧翼区的DNA序列比较揭示了几个共享的短序列元件。(摘要截短至400字)