Conraths F J, Schützle B, Schares G, Christ H, Hobom G, Zahner H
Institut für Parasitologie, Justus-Liebig-Universität, Giessen, Germany.
Mol Biochem Parasitol. 1993 Jul;60(1):111-20. doi: 10.1016/0166-6851(93)90034-u.
The transcription and translation of the gene encoding gp22, a major constituent of the microfilarial sheath of the filarial parasite Litomosoides carinii were studied by in situ hybridisation and immunohistology. Transcription of the gp22 gene is confined to oocytes and embryos in the reproductive organs of adult female worms. It starts in oocytes in the rhachis zone, is maximal in multicellular embryos and decreases slowly as the microfilariae develop. Blood microfilariae lack the gp22 transcript. The gp22 gene product is first detectable in parasites recovered on day 32 post infection. Expression of gp22 begins in multicellular embryos in the uteri of mature female worms and can be detected in all further developed intrauterine stages. The gp22 gene product appears to be exported by the embryonic cells and becomes integrated into the sheath where it may contribute to the flexibility of the latter structure.
利用原位杂交和免疫组织学方法,对丝虫寄生虫卡里尼丝虫微丝蚴鞘主要成分gp22编码基因的转录和翻译进行了研究。gp22基因的转录局限于成年雌虫生殖器官中的卵母细胞和胚胎。它起始于中轴区的卵母细胞,在多细胞胚胎中达到最大值,并随着微丝蚴的发育而缓慢下降。血液中的微丝蚴缺乏gp22转录本。gp22基因产物在感染后第32天回收的寄生虫中首次可检测到。gp22的表达始于成熟雌虫子宫内的多细胞胚胎,并可在所有进一步发育的子宫内阶段检测到。gp22基因产物似乎由胚胎细胞输出,并整合到鞘中,可能有助于后者结构的柔韧性。