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一种阐明真核生物铁代谢的遗传学方法。

A genetic approach to elucidating eukaryotic iron metabolism.

作者信息

Klausner R D, Dancis A

机构信息

Cell Biology and Metabolism Branch, NICHD, NIH, Bethesda, MD 20892.

出版信息

FEBS Lett. 1994 Nov 28;355(2):109-13. doi: 10.1016/0014-5793(94)01111-7.

DOI:10.1016/0014-5793(94)01111-7
PMID:7982480
Abstract

Studies of mutants of the yeast Saccharomyces cerevisiae have led to the identification of genes required for high affinity iron uptake. Reduction of iron (III) outside the cell is accomplished by means of reductases encoded by FRE1 and FRE2, homologues of the gp91-phox component of the oxygen reductase of human granulocytes. High affinity iron (II) transport from the exterior to the interior of the cell occurs by means of a transport system that has not been molecularly characterized. However, the transport process requires the activity of a copper-containing oxidase encoded by FET3. The amino acid sequence of this protein resembles other multi-copper oxidases, including mammalian ceruloplasmin. High affinity copper uptake mediated by the copper transport protein encoded by CTR1 is required to provide the FET3 protein with copper, and thus copper uptake is indirectly required for ferrous iron uptake. These genetic elements of yeast and their relationships may be conserved in complex eukaryotic organisms.

摘要

对酿酒酵母突变体的研究已导致鉴定出高亲和力铁摄取所需的基因。细胞外铁(III)的还原是通过由FRE1和FRE2编码的还原酶完成的,FRE1和FRE2是人类粒细胞氧还原酶的gp91-phox成分的同源物。细胞外高亲和力铁(II)从细胞外转运到细胞内是通过一个尚未进行分子特征描述的转运系统实现的。然而,转运过程需要由FET3编码的含铜氧化酶的活性。该蛋白质的氨基酸序列类似于其他多铜氧化酶,包括哺乳动物的铜蓝蛋白。由CTR1编码的铜转运蛋白介导的高亲和力铜摄取是为FET3蛋白提供铜所必需的,因此亚铁摄取间接需要铜摄取。酵母的这些遗传元件及其关系可能在复杂的真核生物中保守。

相似文献

1
A genetic approach to elucidating eukaryotic iron metabolism.一种阐明真核生物铁代谢的遗传学方法。
FEBS Lett. 1994 Nov 28;355(2):109-13. doi: 10.1016/0014-5793(94)01111-7.
2
Molecular biology of iron acquisition in Saccharomyces cerevisiae.酿酒酵母中铁摄取的分子生物学
Mol Microbiol. 1996 Apr;20(1):27-34. doi: 10.1111/j.1365-2958.1996.tb02485.x.
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AFT1: a mediator of iron regulated transcriptional control in Saccharomyces cerevisiae.AFT1:酿酒酵母中铁调节转录控制的一种介导因子。
EMBO J. 1995 Mar 15;14(6):1231-9. doi: 10.1002/j.1460-2075.1995.tb07106.x.
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Metalloregulation of FRE1 and FRE2 homologs in Saccharomyces cerevisiae.酿酒酵母中FRE1和FRE2同源物的金属调控
J Biol Chem. 1998 Sep 11;273(37):23716-21. doi: 10.1074/jbc.273.37.23716.
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The AFT1 transcriptional factor is differentially required for expression of high-affinity iron uptake genes in Saccharomyces cerevisiae.AFT1转录因子对于酿酒酵母中高亲和力铁摄取基因的表达有不同的需求。
Yeast. 1997 Jun 15;13(7):621-37. doi: 10.1002/(SICI)1097-0061(19970615)13:7<621::AID-YEA121>3.0.CO;2-U.
6
Cytochrome P-450 reductase is responsible for the ferrireductase activity associated with isolated plasma membranes of Saccharomyces cerevisiae.细胞色素P-450还原酶负责与酿酒酵母分离的质膜相关的铁还原酶活性。
FEMS Microbiol Lett. 1997 Nov 1;156(1):147-52. doi: 10.1111/j.1574-6968.1997.tb12720.x.
7
Genetic analysis of iron uptake in the yeast Saccharomyces cerevisiae.酿酒酵母中铁摄取的遗传分析。
J Pediatr. 1998 Mar;132(3 Pt 2):S24-9. doi: 10.1016/s0022-3476(98)70524-4.
8
Evidence for Cu(II) reduction as a component of copper uptake by Saccharomyces cerevisiae.铜(II)还原作为酿酒酵母摄取铜的一个组成部分的证据。
J Biol Chem. 1995 Jan 6;270(1):128-34. doi: 10.1074/jbc.270.1.128.
9
Reductive iron uptake by Candida albicans: role of copper, iron and the TUP1 regulator.白色念珠菌对还原性铁的摄取:铜、铁及TUP1调节因子的作用
Microbiology (Reading). 2002 Jan;148(Pt 1):29-40. doi: 10.1099/00221287-148-1-29.
10
Two distinctly regulated genes are required for ferric reduction, the first step of iron uptake in Saccharomyces cerevisiae.在酿酒酵母中,铁摄取的第一步即铁还原需要两个调控方式截然不同的基因。
Mol Cell Biol. 1994 May;14(5):3065-73. doi: 10.1128/mcb.14.5.3065-3073.1994.

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