• 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

雄性特异性转录的基因编码Ancylostoma 属的 ASPs 和 Kunitz 型蛋白酶抑制剂。

Male-enriched transcription of genes encoding ASPs and Kunitz-type protease inhibitors in Ancylostoma species.

机构信息

Departamento de Parasitologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Avenida Presidente Antônio Carlos 6627, Campus Pampulha, CEP 31270-901 Belo Horizonte, Minas Gerais, Brazil.

出版信息

Mol Cell Probes. 2009 Dec;23(6):298-303. doi: 10.1016/j.mcp.2009.07.004. Epub 2009 Jul 29.

DOI:10.1016/j.mcp.2009.07.004
PMID:19646525
Abstract

Various transcripts coding for proteins considered to be central to parasite-host interactions were identified previously as male-enriched in the hookworm Ancylostoma braziliense. Among these genes were an ASP-5-like homologue and a Kunitz-type protease inhibitor. The present study extends this previous work to investigate similar molecules in other hookworms (Ancylostomatidae). Specifically, partial cDNA sequences encoding three different ASP molecules and two different Kunitz-type protease inhibitors were isolated, and the differential transcription between adult male and female worms was compared by conventional and quantitative reverse transcription (RT)-PCR for three species, A. braziliense, Ancylostoma caninum and Ancylostoma ceylanicum. In accordance with previous findings, male-enriched transcription was observed for all molecules explored. Based on this information, it is hypothesized that adult males are responsible for producing proteins essential to the survival of hookworms inside the host and for supporting developmental and reproductive processes in female worms.

摘要

先前已鉴定出与寄生虫-宿主相互作用相关的蛋白质的各种转录本,在巴西钩虫Ancylostoma braziliense 中被认为是雄性富集的。这些基因包括一个 ASP-5 样同源物和一个 Kunitz 型蛋白酶抑制剂。本研究扩展了之前的工作,以研究其他钩虫(Ancylostomatidae)中的类似分子。具体来说,通过常规和定量逆转录(RT)-PCR 分离编码三种不同 ASP 分子和两种不同 Kunitz 型蛋白酶抑制剂的部分 cDNA 序列,并比较了三种物种(巴西钩虫 Ancylostoma braziliense、犬钩虫Ancylostoma caninum 和斯里兰卡钩虫Ancylostoma ceylanicum)的雌雄成虫之间的差异转录。与先前的发现一致,所有探索的分子都观察到雄性富集转录。基于这些信息,可以假设雄性成虫负责产生对钩虫在宿主内生存至关重要的蛋白质,并支持雌性成虫的发育和生殖过程。

相似文献

1
Male-enriched transcription of genes encoding ASPs and Kunitz-type protease inhibitors in Ancylostoma species.雄性特异性转录的基因编码Ancylostoma 属的 ASPs 和 Kunitz 型蛋白酶抑制剂。
Mol Cell Probes. 2009 Dec;23(6):298-303. doi: 10.1016/j.mcp.2009.07.004. Epub 2009 Jul 29.
2
Identification of gender-regulated genes in Ancylostoma braziliense by real-time RT-PCR.通过实时逆转录聚合酶链反应鉴定巴西钩口线虫中的性别调控基因。
Vet Parasitol. 2008 May 31;153(3-4):277-84. doi: 10.1016/j.vetpar.2008.02.005. Epub 2008 Feb 16.
3
Cloning and characterisation of an aspartyl protease inhibitor (API-1) from Ancylostoma hookworms.来自钩虫的天冬氨酸蛋白酶抑制剂(API-1)的克隆与特性分析
Int J Parasitol. 2005 Mar;35(3):303-13. doi: 10.1016/j.ijpara.2004.11.014. Epub 2005 Jan 8.
4
Confirmation of sex-specific transcripts from Ancylostoma caninum adult worms by semi-quantitative RT-PCR.通过半定量逆转录聚合酶链反应证实犬钩口线虫成虫的性别特异性转录本
Res Vet Sci. 2007 Apr;82(2):215-7. doi: 10.1016/j.rvsc.2006.07.002. Epub 2006 Sep 26.
5
Molecular cloning of a novel multidomain Kunitz-type proteinase inhibitor from the hookworm Ancylostoma caninum.来自犬钩虫的一种新型多结构域库尼茨型蛋白酶抑制剂的分子克隆
J Parasitol. 2003 Apr;89(2):402-7. doi: 10.1645/0022-3395(2003)089[0402:MCOANM]2.0.CO;2.
6
A case of mistaken identity--reappraisal of the species of canid and felid hookworms (Ancylostoma) present in Australia and India.一例身份误认——对澳大利亚和印度存在的犬科和猫科钩虫(钩口线虫属)物种的重新评估
Parasitology. 2007 Jan;134(Pt 1):113-9. doi: 10.1017/S0031182006001211. Epub 2006 Sep 21.
7
Application of a species-specific PCR-RFLP to identify Ancylostoma eggs directly from canine faeces.应用种特异性聚合酶链反应-限制性片段长度多态性技术直接从犬粪便中鉴定钩虫卵。
Vet Parasitol. 2004 Sep 2;123(3-4):245-55. doi: 10.1016/j.vetpar.2004.05.026.
8
Cloning, yeast expression, isolation, and vaccine testing of recombinant Ancylostoma-secreted protein (ASP)-1 and ASP-2 from Ancylostoma ceylanicum.来自锡兰钩虫的重组钩虫分泌蛋白(ASP)-1和ASP-2的克隆、酵母表达、分离及疫苗测试
J Infect Dis. 2004 Mar 1;189(5):919-29. doi: 10.1086/381901. Epub 2004 Feb 6.
9
Differential diagnosis of dog hookworms based on PCR-RFLP from the ITS region of their rDNA.基于核糖体DNA ITS区域的PCR-RFLP技术对犬钩虫的鉴别诊断
Vet Parasitol. 2006 Sep 10;140(3-4):373-7. doi: 10.1016/j.vetpar.2006.04.012. Epub 2006 May 18.
10
Gene expression profiles associated with the transition to parasitism in Ancylostoma caninum larvae.与犬钩虫幼虫向寄生状态转变相关的基因表达谱
Mol Biochem Parasitol. 2005 Sep;143(1):39-48. doi: 10.1016/j.molbiopara.2005.04.012.

引用本文的文献

1
Hookworm genes encoding intestinal excreted-secreted proteins are transcriptionally upregulated in response to the host's immune system.编码肠道排泄分泌蛋白的钩虫基因在宿主免疫系统的作用下转录上调。
bioRxiv. 2025 Feb 3:2025.02.01.636063. doi: 10.1101/2025.02.01.636063.
2
Twenty-five-year research progress in hookworm excretory/secretory products.钩虫排泄/分泌产物 25 年研究进展。
Parasit Vectors. 2020 Mar 14;13(1):136. doi: 10.1186/s13071-020-04010-8.
3
Sex-biased gene expression and sequence conservation in Atlantic and Pacific salmon lice (Lepeophtheirus salmonis).
大西洋鲑鱼虱和太平洋鲑鱼虱(鲑鱼虱属)中的性别偏向基因表达与序列保守性
BMC Genomics. 2016 Jul 4;17:483. doi: 10.1186/s12864-016-2835-7.
4
Twenty-first century progress toward the global control of human hookworm infection.21 世纪全球控制人类钩虫感染的进展。
Curr Infect Dis Rep. 2011 Jun;13(3):210-7. doi: 10.1007/s11908-011-0182-z.
5
Identification and characterization of a serine protease inhibitor with two trypsin inhibitor-like domains from the human hookworm Ancylostoma duodenale.鉴定和表征人十二指肠钩虫Ancylostoma duodenale 中的一种具有两个胰蛋白酶抑制剂样结构域的丝氨酸蛋白酶抑制剂。
Parasitol Res. 2011 Feb;108(2):287-95. doi: 10.1007/s00436-010-2055-z. Epub 2010 Sep 18.
6
Massively parallel sequencing and analysis of the Necator americanus transcriptome.大规模平行测序和分析美洲钩虫转录组。
PLoS Negl Trop Dis. 2010 May 11;4(5):e684. doi: 10.1371/journal.pntd.0000684.