Dancis A
Cell Biology and Metabolism Branch, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA.
J Pediatr. 1998 Mar;132(3 Pt 2):S24-9. doi: 10.1016/s0022-3476(98)70524-4.
We used the methods of yeast genetics to identify genes involved in acquisition of iron by eukaryotic cells.
Mutants were identified with defects in cellular iron uptake. These were organized into an upstream group and a downstream group. The upstream group was involved in the delivery of copper to the multicopper oxidase FET3. Mutants of this group were characterized by defective iron uptake that could be corrected by exposure of the cells to large amounts of copper. The downstream group was more directly involved in iron uptake. Mutant phenotypes from these genes could not be corrected by copper exposure.
Genes in the upstream group encoded the regulator of copper transport, MAC1, and two copper transporters, CTR1 and CCC2. Genes in the downstream group encoded the multicopper oxidase FET3 and its partner the iron permease FTR1. In addition, the downstream genes encoded the surface reductases FRE1 and FRE2 and the iron regulatory protein AFT1.
The iron and copper uptake processes in yeast intersect because the FET3 gene encodes a multicopper oxidase that is required for iron transport. In human beings, an analogous function may be served by ceruloplasmin, a multicopper oxidase with a role in iron homeostasis.
我们运用酵母遗传学方法来鉴定真核细胞获取铁过程中涉及的基因。
鉴定出细胞铁摄取存在缺陷的突变体。这些突变体被分为上游组和下游组。上游组参与将铜传递至多铜氧化酶FET3。该组突变体的特征是铁摄取存在缺陷,可通过将细胞暴露于大量铜来纠正。下游组更直接参与铁摄取。这些基因的突变体表型不能通过铜暴露来纠正。
上游组的基因编码铜转运调节因子MAC1以及两种铜转运蛋白CTR1和CCC2。下游组的基因编码多铜氧化酶FET3及其伴侣铁通透酶FTR1。此外,下游基因编码表面还原酶FRE1和FRE2以及铁调节蛋白AFT1。
酵母中的铁摄取和铜摄取过程相互交叉,因为FET3基因编码一种铁转运所需的多铜氧化酶。在人类中,一种类似的功能可能由铜蓝蛋白来发挥,铜蓝蛋白是一种在铁稳态中起作用的多铜氧化酶。