首页> 外文期刊>Proceedings of the National Academy of Sciences of the United States of America >Epigenetic control of the variable expression of a Plasmodium falciparum receptor protein for erythrocyte invasion
【24h】

Epigenetic control of the variable expression of a Plasmodium falciparum receptor protein for erythrocyte invasion

机译:恶性疟原虫受体蛋白对红细胞侵袭的可变表达的表观遗传控制

获取原文
获取原文并翻译 | 示例
       

摘要

Plasmodium falciparum can invade erythrocytes by redundant receptors, some of which have variable expression. A P. falciparum clone Dd2 requiring erythrocyte sialic acid for invasion can be switched to a sialic acid-independent progeny clone Dd2NM by growing the Dd2 clone with neuraminidase-treated erythrocytes. The RH4 gene is transcriptionally up-regulated in Dd2NM compared to Dd2, despite the absence of DNA changes in and around the gene. We determined the epigenetic modifications around the transcription start site (TSS) at the time of expression of RH4 in Dd2NM (44 h) and at an earlier time when RH4 is not expressed (24 h). At 44 h, the occupancy of the +1 nucleosome site downstream of the TSS of the active RH4 gene in Dd2NM was markedly reduced compared to Dd2; no difference was observed at 24 h. At 44 h, histone modifications associated with up-regulation were positively correlated to the active RH4 gene of Dd2NM compared to Dd2; no differences were observed at 24 h. Histone H3K9 trimethylation (a marker for silencing) was higher in Dd2 than Dd2NM along the 5-UTRs of the RH4 gene at both 44 and 24 h. Our data indicate that the failure of Dd2 to express the sialic acid-independent invasion receptor gene RH4 is associated with the epigenetic silencing mark H3K9 trimethylation present throughout the cycle.
机译:恶性疟原虫可以通过多余的受体侵入红细胞,其中一些受体具有可变的表达。通过用神经氨酸酶处理的红细胞使Dd2克隆生长,可以将需要红细胞唾液酸入侵的恶性疟原虫克隆Dd2切换为不依赖唾液酸的后代克隆Dd2NM。与Dd2相比,RHd4基因在Dd2NM中的转录上调,尽管该基因及其周围没有DNA改变。我们确定了在Dd2NM中表达RH4时(44小时)和不表达RH4的较早时间(24小时)周围转录起始位点(TSS)的表观遗传修饰。在第44小时,与Dd2相比,Dd2NM中活性RH4基因的TSS下游+1核小体位点的占有率显着降低。 24小时未观察到差异。与Dd2相比,在44 h时,与上调相关的组蛋白修饰与Dd2NM的活性RH4基因正相关。 24小时未观察到差异。在第44和24小时,沿着RH4基因的5-UTR,组蛋白H3K9三甲基化(沉默的标志)在Dd2中高于Dd2NM。我们的数据表明,Dd2表达唾液酸非依赖性入侵受体基因RH4的失败与整个周期中存在的表观遗传沉默标记H3K9三甲基化有关。

著录项

  • 来源
  • 作者单位

    Laboratory of Malaria Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD 20852;

    rnLaboratory of Malaria Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD 20852;

    rnLaboratory of Malaria Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD 20852;

    rnLaboratory of Malaria Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD 20852;

    rnLaboratory of Malaria Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD 20852;

    rnLaboratory of Molecular Immunology, The National Heart, Lung, and Blood Institute, National Institutes of Health, Bethesda, MD 20892;

    rnLaboratory of Molecular Biology, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, MD 20892;

    rnLaboratory of Malaria Vector Research, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Rockville, MD 20852;

  • 收录信息 美国《科学引文索引》(SCI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

    epigenetic mark; histone modification; nucleosome;

    机译:表观遗传标记组蛋白修饰;核小体;
  • 入库时间 2022-08-18 00:41:11

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号