• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

恶性疟原虫中钙调蛋白基因的阶段特异性表达。

Stage-specific expression of the calmodulin gene in Plasmodium falciparum.

作者信息

Orfa Rojas M, Wasserman M

机构信息

Facultad de Ciencias Universidad Nacional, Bogotá, Colombia.

出版信息

J Biochem. 1995 Dec;118(6):1118-23. doi: 10.1093/oxfordjournals.jbchem.a124996.

DOI:10.1093/oxfordjournals.jbchem.a124996
PMID:8720124
Abstract

We studied the synthesis of calmodulin mRNA and of calmodulin during the asexual cell cycle of Plasmodium falciparum. The expression of the gene was low during the early stages of the erythrocytic asexual cycle. When the parasites were 28 h old the level of mRNA increased steadily to reach a peak at the age of 40 h. During the last 8 h of the cycle a constant decrease in the amount of calmodulin mRNA was observed. The synthesis of the protein followed the expression pattern of the mRNA, but without the final decrease. The average amounts of calmodulin measured were 2.5 +/- 0.9 ng/10(8) 14-h-old rings, 4.38 +/- 0.35 ng/10(8) 36-h-old trophozoites, 11.8 +/- 1.45 ng/10(8) 44-h-old trophozoites, and 19.6 +/- 1.9 ng/10(8) 48-h-old schizonts. The in vivo stability of mRNA in different developmental stages was evaluated by pulse and chase experiments. The RNA of very mature trophozoites was quickly degraded, in contrast with the high stability shown by the RNA in other stages. The results here suggest that the calmodulin gene expression in Plasmodium does not follow a housekeeping pattern of expression such as in other eukaryotic cells, but that it is regulated at the level of transcription and RNA degradation.

摘要

我们研究了恶性疟原虫无性细胞周期中钙调蛋白mRNA及钙调蛋白的合成。在红细胞无性周期的早期阶段,该基因的表达水平较低。当疟原虫发育至28小时龄时,mRNA水平稳步上升,并在40小时龄时达到峰值。在周期的最后8小时内,观察到钙调蛋白mRNA的量持续下降。蛋白质的合成遵循mRNA的表达模式,但没有最后的下降阶段。所测得的钙调蛋白平均量分别为:14小时龄环状体为2.5±0.9 ng/10⁸个;36小时龄滋养体为4.38±0.35 ng/10⁸个;44小时龄滋养体为11.8±1.45 ng/10⁸个;48小时龄裂殖体为19.6±1.9 ng/10⁸个。通过脉冲追踪实验评估了不同发育阶段mRNA在体内的稳定性。与其他阶段RNA所显示的高稳定性相反,非常成熟的滋养体的RNA迅速降解。这里的结果表明,疟原虫中钙调蛋白基因的表达并不遵循如其他真核细胞那样的持家基因表达模式,而是在转录和RNA降解水平受到调控。

相似文献

1
Stage-specific expression of the calmodulin gene in Plasmodium falciparum.恶性疟原虫中钙调蛋白基因的阶段特异性表达。
J Biochem. 1995 Dec;118(6):1118-23. doi: 10.1093/oxfordjournals.jbchem.a124996.
2
Differential transcription of histone genes in asexual and sexual stages of Plasmodium falciparum.
Int J Parasitol. 1999 Sep;29(9):1447-9. doi: 10.1016/s0020-7519(99)00090-9.
3
Whole-genome analysis of mRNA decay in Plasmodium falciparum reveals a global lengthening of mRNA half-life during the intra-erythrocytic development cycle.恶性疟原虫mRNA降解的全基因组分析揭示了红细胞内发育周期中mRNA半衰期的整体延长。
Genome Biol. 2007;8(7):R134. doi: 10.1186/gb-2007-8-7-r134.
4
Expression of housekeeping genes during the asexual cell cycle of Plasmodium falciparum.恶性疟原虫无性细胞周期中管家基因的表达
Parasitol Res. 2002 Mar;88(3):267-71. doi: 10.1007/s00436-001-0526-y.
5
Use of variability in the stage-specific transcription levels of Plasmodium falciparum in the selection of target genes.利用恶性疟原虫阶段特异性转录水平的变异性来选择靶基因。
Parasitol Int. 2001 Sep;50(3):165-73. doi: 10.1016/s1383-5769(01)00075-7.
6
[Transcription profile of PfRON4 gene in Plasmodium falciparum erythrocytic stage].[恶性疟原虫红细胞内期PfRON4基因的转录谱]
Zhongguo Ji Sheng Chong Xue Yu Ji Sheng Chong Bing Za Zhi. 2009 Jun;27(3):206-9.
7
PfMyb1, a Plasmodium falciparum transcription factor, is required for intra-erythrocytic growth and controls key genes for cell cycle regulation.PfMyb1是一种恶性疟原虫转录因子,是红细胞内生长所必需的,并控制细胞周期调控的关键基因。
J Mol Biol. 2005 Feb 11;346(1):29-42. doi: 10.1016/j.jmb.2004.11.045. Epub 2004 Dec 21.
8
Global analysis of transcript and protein levels across the Plasmodium falciparum life cycle.恶性疟原虫生命周期中转录本和蛋白质水平的全局分析。
Genome Res. 2004 Nov;14(11):2308-18. doi: 10.1101/gr.2523904.
9
Antisense oligonucleotides targeting malarial aldolase inhibit the asexual erythrocytic stages of Plasmodium falciparum.靶向疟原虫醛缩酶的反义寡核苷酸可抑制恶性疟原虫的无性红细胞期。
Mol Biochem Parasitol. 1999 Jul 30;102(1):91-101. doi: 10.1016/s0166-6851(99)00087-0.
10
Plasmodium falciparum: alterations in organelle transcript abundance during the erythrocytic cycle.恶性疟原虫:红细胞内期循环中细胞器转录本丰度的变化
Exp Parasitol. 1995 May;80(3):430-40. doi: 10.1006/expr.1995.1055.

引用本文的文献

1
Identification of putative potassium channel homologues in pathogenic protozoa.鉴定致病原生动物中的假定钾通道同源物。
PLoS One. 2012;7(2):e32264. doi: 10.1371/journal.pone.0032264. Epub 2012 Feb 21.
2
Quantitative proteomics reveals new insights into erythrocyte invasion by Plasmodium falciparum.定量蛋白质组学揭示了恶性疟原虫入侵红细胞的新见解。
Mol Cell Proteomics. 2012 Feb;11(2):M111.010645. doi: 10.1074/mcp.M111.010645. Epub 2011 Oct 24.
3
Role of cis-regulatory elements on the ring-specific hrp3 promoter in the human parasite Plasmodium falciparum.
环特异性 hrp3 启动子 cis 调控元件在人类寄生虫疟原虫中的作用。
Parasitol Res. 2010 Mar;106(4):833-45. doi: 10.1007/s00436-010-1738-9. Epub 2010 Feb 3.
4
An enhancer-like region regulates hrp3 promoter stage-specific gene expression in the human malaria parasite Plasmodium falciparum.一个类似增强子的区域调控人类疟原虫恶性疟原虫中hrp3启动子的阶段特异性基因表达。
Biochim Biophys Acta. 2007 Jul-Aug;1769(7-8):506-13. doi: 10.1016/j.bbaexp.2007.04.009. Epub 2007 May 8.