畜牧兽医学报 ›› 2022, Vol. 53 ›› Issue (5): 1354-1363.doi: 10.11843/j.issn.0366-6964.2022.05.004

• 综述 • 上一篇    下一篇

恶性疟原虫ApiAP2蛋白质家族研究进展

郑雨昕, 张义伟, 姜宁*   

  1. 沈阳农业大学动物科学与医学学院, 沈阳 110161
  • 收稿日期:2021-07-30 出版日期:2022-05-23 发布日期:2022-05-25
  • 通讯作者: 姜宁,主要从事人畜共患病相关研究,E-mail:jiangning1969@163.com
  • 作者简介:郑雨昕(1998-),女,蒙古族,辽宁喀左人,硕士生,主要从事人兽共患寄生虫病研究,E-mail:zheng_yuxin2021@163.com
  • 基金资助:
    国家自然科学基金(81772219)

Research Advance on ApiAP2 Family of Plasmodium falciparum

ZHENG Yuxin, ZHANG Yiwei, JIANG Ning*   

  1. College of Animal Science and Veterinary Medicine, Shenyang Agricultural University, Shenyang 110161, China
  • Received:2021-07-30 Online:2022-05-23 Published:2022-05-25

摘要: 疟疾是由顶复门寄生虫——疟原虫引起的一种人畜共患病。疟原虫不仅可以感染人,还能够感染家禽、鼠、食蟹猴等多种动物,其中,鸡疟原虫病、鼠疟原虫病对畜牧业影响较大。为完成其复杂的生命周期,疟原虫需要严格的基因调控,而转录因子对基因表达的调控作用十分关键。截至目前,ApiAP2 蛋白质家族是在所有顶复门原虫中作为候选转录因子出现的唯一蛋白质家族。论文在总结已有研究的基础上,预测恶性疟原虫ApiAP2 蛋白质家族中未知功能蛋白质的调控机制,并开展对ApiAP2 蛋白质家族发生蛋白质翻译后修饰功能的展望,为畜牧业研发原虫病疫苗提供借鉴与参考。

关键词: 疟疾, 恶性疟原虫, ApiAP2蛋白质家族, 基因调控, 转录因子, 蛋白质翻译后修饰

Abstract: Malaria is a zoonosis caused by Plasmodium which belongs to Apicomplexan. Plasmodium can not only infect human beings, but also poultries, mice, cynomolgus macaques and many kinds of animals, among which Plasmodium gallinaceum and rodent malaria have a great impact on animal husbandry. Plasmodium requires a strict gene regulation to complete its complex life cycle and transcription factors play very essential roles in regulating gene expression. Up to now, apicomplexan AP2 (ApiAP2) family is the only candidate that appears as transcription factors in Apicomplexan. On the basis of summarizing the previous studies, this article predicts the regulatory mechanism that the function of proteins is unknown in ApiAP2 family of Plasmodium falciparum, also explores the prospect of the post-translational modification in ApiAP2 family, which provides reference for animal husbandry to develop vaccine of protozoal diseases.

Key words: malaria, Plasmodium falciparum, ApiAP2 protein family, gene regulation, transcription factor, post-translational modification

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