• 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

恶性疟原虫染色体的长程限制图谱:地理上遥远分离株之间的交叉与大小变异

Long-range restriction maps of Plasmodium falciparum chromosomes: crossingover and size variation among geographically distant isolates.

作者信息

Sinnis P, Wellems T E

机构信息

Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, Bethesda, Maryland 20892.

出版信息

Genomics. 1988 Nov;3(4):287-95. doi: 10.1016/0888-7543(88)90117-6.

DOI:10.1016/0888-7543(88)90117-6
PMID:3072285
Abstract

Homologous chromosomes from the human malaria parasite Plasmodium falciparum exhibit striking size polymorphism from isolate to isolate. To examine the structural basis for these variations, we have determined full-length restriction maps of chromosome 4 from three P. falciparum clones. Two clones, HB3 and 3D7, are derived from geographically distant strains, while the third, XP5, is the product of an HB3/3D7 cross. The restriction maps show that, while the overall structure and organization of chromosome 4 from each clone are similar, large-scale variations occur within a few hundred kilobase pairs of the chromosome ends. An apparent crossover between the 3D7 and the HB3 parent chromosomes accounts for a chromosome of intermediate size in clone XP5. Similar restriction studies extended to other parasite chromosomes will ultimately yield a long-range physical map of the P. falciparum genome.

摘要

来自人类疟原虫恶性疟原虫的同源染色体在不同分离株之间表现出显著的大小多态性。为了研究这些变异的结构基础,我们确定了来自三个恶性疟原虫克隆的4号染色体的全长限制性图谱。两个克隆HB3和3D7来自地理上遥远的菌株,而第三个克隆XP5是HB3/3D7杂交的产物。限制性图谱表明,虽然每个克隆的4号染色体的总体结构和组织相似,但在染色体末端的几百千碱基对内发生了大规模变异。3D7和HB3亲本染色体之间明显的交叉导致了克隆XP5中出现中等大小的染色体。扩展到其他寄生虫染色体的类似限制性研究最终将产生恶性疟原虫基因组的长程物理图谱。

相似文献

1
Long-range restriction maps of Plasmodium falciparum chromosomes: crossingover and size variation among geographically distant isolates.恶性疟原虫染色体的长程限制图谱:地理上遥远分离株之间的交叉与大小变异
Genomics. 1988 Nov;3(4):287-95. doi: 10.1016/0888-7543(88)90117-6.
2
Chromosome 9 from independent clones and isolates of Plasmodium falciparum undergoes subtelomeric deletions with similar breakpoints in vitro.
Mol Biochem Parasitol. 1990 Apr;40(1):137-45. doi: 10.1016/0166-6851(90)90087-3.
3
Rapid whole genome optical mapping of Plasmodium falciparum.快速全基因组光学图谱绘制恶性疟原虫。
Malar J. 2011 Aug 26;10:252. doi: 10.1186/1475-2875-10-252.
4
Interchromosomal exchange of a large subtelomeric segment in a Plasmodium falciparum cross.恶性疟原虫杂交中一个大的亚端粒片段的染色体间交换。
EMBO J. 1994 Sep 1;13(17):4174-80. doi: 10.1002/j.1460-2075.1994.tb06735.x.
5
Repetitive sequences upstream of the pfg27/25 gene determine polymorphism in laboratory and natural lines of Plasmodium falciparum.恶性疟原虫实验室株和自然株中,pfg27/25基因上游的重复序列决定了其多态性。
Mol Biochem Parasitol. 2000 Oct;110(2):247-57. doi: 10.1016/s0166-6851(00)00274-7.
6
A genetic map and recombination parameters of the human malaria parasite Plasmodium falciparum.人类疟原虫恶性疟原虫的遗传图谱及重组参数
Science. 1999 Nov 12;286(5443):1351-3. doi: 10.1126/science.286.5443.1351.
7
Genetic hypervariability of telomere-related sequences is associated with meiosis in Plasmodium falciparum.端粒相关序列的遗传高变异性与恶性疟原虫的减数分裂有关。
Nucleic Acids Res. 1988 Jul 25;16(14B):6973-85. doi: 10.1093/nar/16.14.6973.
8
Chromosomes of malaria parasites.
Trends Genet. 1989 Oct;5(10):337-42. doi: 10.1016/0168-9525(89)90139-x.
9
7H8/6, a multicopy DNA probe for distinguishing isolates of Plasmodium falciparum.7H8/6,一种用于区分恶性疟原虫分离株的多拷贝DNA探针。
Mol Biochem Parasitol. 1991 Aug;47(2):197-206. doi: 10.1016/0166-6851(91)90179-a.
10
Kinetic and molecular properties of the dihydrofolate reductase from pyrimethamine-sensitive and pyrimethamine-resistant clones of the human malaria parasite Plasmodium falciparum.来自人类疟原虫恶性疟原虫的乙胺嘧啶敏感和耐药克隆的二氢叶酸还原酶的动力学和分子特性。
Mol Pharmacol. 1987 Apr;31(4):430-7.

引用本文的文献

1
Genomics and Genetics: New Insights into Malaria Pathogenesis, Drug Resistance, Epidemiology, and Evolution.基因组学与遗传学:疟疾发病机制、耐药性、流行病学和进化的新见解。
Clin Microbiol Rev. 2019 Jul 31;32(4). doi: 10.1128/CMR.00019-19. Print 2019 Sep 18.
2
Profile of Thomas E. Wellems.托马斯·E·韦勒姆斯简介。
Proc Natl Acad Sci U S A. 2010 Aug 3;107(31):13567-9. doi: 10.1073/pnas.1008826107. Epub 2010 Jul 19.
3
Targeted terminal deletions as a tool for functional genomics studies in Plasmodium.靶向末端缺失作为疟原虫功能基因组学研究的一种工具。
Genome Res. 2000 Sep;10(9):1414-20. doi: 10.1101/gr.140000.
4
Optical mapping of Plasmodium falciparum chromosome 2.恶性疟原虫2号染色体的光学图谱
Genome Res. 1999 Feb;9(2):175-81.
5
Malaria's Eve: evidence of a recent population bottleneck throughout the world populations of Plasmodium falciparum.疟疾前夕:恶性疟原虫全球种群近期出现种群瓶颈的证据。
Proc Natl Acad Sci U S A. 1998 Apr 14;95(8):4425-30. doi: 10.1073/pnas.95.8.4425.
6
Expressed var genes are found in Plasmodium falciparum subtelomeric regions.在恶性疟原虫的亚端粒区域发现了表达的var基因。
Mol Cell Biol. 1997 Feb;17(2):604-11. doi: 10.1128/MCB.17.2.604.
7
The var genes of Plasmodium falciparum are located in the subtelomeric region of most chromosomes.恶性疟原虫的变异基因位于大多数染色体的亚端粒区域。
EMBO J. 1996 Aug 1;15(15):4069-77.
8
Interchromosomal exchange of a large subtelomeric segment in a Plasmodium falciparum cross.恶性疟原虫杂交中一个大的亚端粒片段的染色体间交换。
EMBO J. 1994 Sep 1;13(17):4174-80. doi: 10.1002/j.1460-2075.1994.tb06735.x.
9
Evidence that a point mutation in dihydrofolate reductase-thymidylate synthase confers resistance to pyrimethamine in falciparum malaria.二氢叶酸还原酶-胸苷酸合成酶中的点突变赋予恶性疟原虫对乙胺嘧啶耐药性的证据。
Proc Natl Acad Sci U S A. 1988 Dec;85(23):9114-8. doi: 10.1073/pnas.85.23.9114.
10
Evidence for a switching mechanism in the invasion of erythrocytes by Plasmodium falciparum.恶性疟原虫侵入红细胞过程中转换机制的证据。
J Clin Invest. 1990 Aug;86(2):618-24. doi: 10.1172/JCI114753.