From the Département de Biochimie, Faculté de Médecine et des Sciences de la Santé, Université de Sherbrooke, Sherbrooke, Quebec J1E 4K8, Canada.
J Biol Chem. 2014 Apr 4;289(14):10168-81. doi: 10.1074/jbc.M113.543678. Epub 2014 Feb 25.
Meiosis requires copper to undertake its program in which haploid gametes are produced from diploid precursor cells. In Schizosaccharomyces pombe, copper is transported by three members of the copper transporter (Ctr) family, namely Ctr4, Ctr5, and Ctr6. Although central for sexual differentiation, very little is known about the expression profile, cellular localization, and physiological contribution of the Ctr proteins during meiosis. Analysis of gene expression of ctr4(+) and ctr5(+) revealed that they are primarily expressed in early meiosis under low copper conditions. In the case of ctr6(+), its expression is broader, being detected throughout the entire meiotic process with an increase during middle- and late-phase meiosis. Whereas the expression of ctr4(+) and ctr5(+) is exclusively dependent on the presence of Cuf1, ctr6(+) gene expression relies on two distinct regulators, Cuf1 and Mei4. Ctr4 and Ctr5 proteins co-localize at the plasma membrane shortly after meiotic induction, whereas Ctr6 is located on the membrane of vacuoles. After meiotic divisions, Ctr4 and Ctr5 disappear from the cell surface, whereas Ctr6 undergoes an intracellular re-location to co-localize with the forespore membrane. Under copper-limiting conditions, disruption of ctr4(+) and ctr6(+) results in altered SOD1 activity, whereas these mutant cells exhibit substantially decreased levels of CAO activity mostly in early- and middle-phase meiosis. Collectively, these results emphasize the notion that Ctr proteins exhibit differential expression, localization, and contribution in delivering copper to SOD1 and Cao1 proteins during meiosis.
减数分裂需要铜来完成其程序,在此过程中,由二倍体前体细胞产生单倍体配子。在酿酒酵母中,铜由三种铜转运蛋白(Ctr)家族成员 Ctr4、Ctr5 和 Ctr6 转运。尽管它们对性别分化至关重要,但对于 Ctr 蛋白在减数分裂过程中的表达谱、细胞定位和生理贡献知之甚少。对 ctr4(+)和 ctr5(+)基因表达的分析表明,它们主要在低铜条件下的早期减数分裂中表达。对于 ctr6(+),其表达更为广泛,在整个减数分裂过程中都有检测到,在中晚期减数分裂中增加。虽然 ctr4(+)和 ctr5(+)的表达完全依赖于 Cuf1 的存在,但 ctr6(+)基因的表达依赖于两个不同的调节剂,Cuf1 和 Mei4。Ctr4 和 Ctr5 蛋白在减数分裂诱导后不久就会在质膜上共定位,而 Ctr6 则位于液泡的膜上。减数分裂后,Ctr4 和 Ctr5 从细胞表面消失,而 Ctr6 则在细胞内重新定位,与前孢子膜共定位。在铜限制条件下,ctr4(+)和 ctr6(+)的破坏会导致 SOD1 活性改变,而这些突变细胞的 CAO 活性显著降低,主要在早期和中期减数分裂中。总之,这些结果强调了 Ctr 蛋白在减数分裂过程中表现出不同的表达、定位和对 SOD1 和 Cao1 蛋白的铜输送的贡献。