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本文引用的文献

1
The diferric-tyrosyl radical cluster of ribonucleotide reductase and cytosolic iron-sulfur clusters have distinct and similar biogenesis requirements.核糖核苷酸还原酶的双铁-酪氨酰自由基簇和胞质铁硫簇具有不同但又相似的生物合成需求。
J Biol Chem. 2017 Jul 7;292(27):11445-11451. doi: 10.1074/jbc.M117.786178. Epub 2017 May 17.
2
The ZIP family zinc transporters support the virulence of Cryptococcus neoformans.ZIP家族锌转运蛋白支持新型隐球菌的毒力。
Med Mycol. 2016 Aug 1;54(6):605-15. doi: 10.1093/mmy/myw013. Epub 2016 Apr 26.
3
The Role of Copper and Zinc Toxicity in Innate Immune Defense against Bacterial Pathogens.铜和锌毒性在针对细菌病原体的固有免疫防御中的作用
J Biol Chem. 2015 Jul 31;290(31):18954-61. doi: 10.1074/jbc.R115.647099. Epub 2015 Jun 8.
4
Functional characterization of new mutations in Wilson disease gene (ATP7B) using the yeast model.利用酵母模型对威尔逊病基因(ATP7B)新突变进行功能表征。
J Trace Elem Med Biol. 2015;31:33-6. doi: 10.1016/j.jtemb.2015.02.006. Epub 2015 Mar 5.
5
Leu1 plays a role in iron metabolism and is required for virulence in Cryptococcus neoformans.亮氨酸1在铁代谢中起作用,是新生隐球菌毒力所必需的。
Fungal Genet Biol. 2015 Feb;75:11-9. doi: 10.1016/j.fgb.2014.12.006. Epub 2014 Dec 29.
6
Extracellular zinc competitively inhibits manganese uptake and compromises oxidative stress management in Streptococcus pneumoniae.细胞外锌竞争性抑制肺炎链球菌对锰的摄取,并损害其氧化应激管理能力。
PLoS One. 2014 Feb 18;9(2):e89427. doi: 10.1371/journal.pone.0089427. eCollection 2014.
7
Transition metal ions at the crossroads of mucosal immunity and microbial pathogenesis.处于黏膜免疫与微生物致病机制交叉点的过渡金属离子。
Front Cell Infect Microbiol. 2014 Jan 24;4:2. doi: 10.3389/fcimb.2014.00002. eCollection 2014.
8
Cryptococcus neoformans copper detoxification machinery is critical for fungal virulence.新生隐球菌铜解毒机制对真菌毒力至关重要。
Cell Host Microbe. 2013 Mar 13;13(3):265-76. doi: 10.1016/j.chom.2013.02.002.
9
Activation of an essential calcium signaling pathway in Saccharomyces cerevisiae by Kch1 and Kch2, putative low-affinity potassium transporters.酿酒酵母中假定的低亲和力钾转运蛋白Kch1和Kch2对一种必需钙信号通路的激活作用。
Eukaryot Cell. 2013 Feb;12(2):204-14. doi: 10.1128/EC.00299-12. Epub 2012 Nov 30.
10
Quantitative imaging of mitochondrial and cytosolic free zinc levels in an in vitro model of ischemia/reperfusion.在缺血/再灌注的体外模型中定量成像线粒体和细胞质游离锌水平。
J Bioenerg Biomembr. 2012 Apr;44(2):253-63. doi: 10.1007/s10863-012-9427-2. Epub 2012 Mar 20.

液泡锌转运蛋白 Zrc1 是人类真菌病原体新型隐球菌细胞内过量锌解毒所必需的。

Vacuolar zinc transporter Zrc1 is required for detoxification of excess intracellular zinc in the human fungal pathogen Cryptococcus neoformans.

机构信息

Department of Systems Biotechnology, Chung-Ang University, Anseong, 17546, Republic of Korea.

Michael Smith Laboratories, University of British Columbia, Vancouver, B.C., V6T 1Z4, Canada.

出版信息

J Microbiol. 2018 Jan;56(1):65-71. doi: 10.1007/s12275-018-7475-y. Epub 2018 Jan 4.

DOI:10.1007/s12275-018-7475-y
PMID:29299844
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7552933/
Abstract

Zinc is an important transition metal in all living organisms and is required for numerous biological processes. However, excess zinc can also be toxic to cells and cause cellular stress. In the model fungus Saccharomyces cerevisiae, a vacuolar zinc transporter, Zrc1, plays important roles in the storage and detoxification of excess intracellular zinc to protect the cell. In this study, we identified an ortholog of the S. cerevisiae ZRC1 gene in the human fungal pathogen Cryptococcus neoformans. Zrc1 was localized in the vacuolar membrane in C. neoformans, and a mutant lacking ZRC1 showed significant growth defects under high-zinc conditions. These results suggested a role for Zrc1 in zinc detoxification. However, contrary to our expectation, the expression of Zrc1 was induced in cells grown in zinc-limited conditions and decreased upon the addition of zinc. These expression patterns were similar to those of Zip1, the high-affinity zinc transporter in the plasma membrane of C. neoformans. Furthermore, we used the zrc1 mutant in a murine model of cryptococcosis to examine whether a mammalian host could inhibit the survival of C. neoformans using zinc toxicity. We found that the mutant showed no difference in virulence compared with the wildtype strain. This result suggests that Zrc1-mediated zinc detoxification is not required for the virulence of C. neoformans, and imply that zinc toxicity may not be an important aspect of the host immune response to the fungus.

摘要

锌是所有生物体内的一种重要过渡金属,是许多生物过程所必需的。然而,过量的锌也可能对细胞有毒,并导致细胞应激。在模式真菌酿酒酵母中,液泡锌转运蛋白 Zrc1 在储存和解毒过量的细胞内锌以保护细胞方面发挥着重要作用。在这项研究中,我们在人类真菌病原体新生隐球菌中鉴定了酿酒酵母 ZRC1 基因的同源物。Zrc1 在 C. neoformans 的液泡膜中定位,并且缺乏 ZRC1 的突变体在高锌条件下表现出明显的生长缺陷。这些结果表明 Zrc1 在锌解毒中起作用。然而,与我们的预期相反,在锌限制条件下生长的细胞中 Zrc1 的表达被诱导,并且在添加锌时表达减少。这些表达模式与新生隐球菌质膜中高亲和力锌转运蛋白 Zip1 的表达模式相似。此外,我们在隐球菌病的小鼠模型中使用 zrc1 突变体来检查哺乳动物宿主是否可以利用锌毒性抑制新生隐球菌的存活。我们发现突变体与野生型菌株相比在毒力上没有差异。该结果表明 Zrc1 介导的锌解毒对于新生隐球菌的毒力不是必需的,并且暗示锌毒性可能不是宿主对真菌免疫反应的一个重要方面。