Dulermo Rémi, Dulermo Thierry, Gamboa-Meléndez Heber, Thevenieau France, Nicaud Jean-Marc
INRA, UMR1319 Micalis, Jouy-en-Josas, France AgroParisTech, UMR Micalis, Jouy-en-Josas, France.
AgroParisTech, UMR Micalis, Jouy-en-Josas, France.
Eukaryot Cell. 2015 May;14(5):511-25. doi: 10.1128/EC.00051-15. Epub 2015 Mar 27.
Peroxisomes are essential organelles in the cells of most eukaryotes, from yeasts to mammals. Their role in β-oxidation is particularly essential in yeasts; for example, in Saccharomyces cerevisiae, fatty acid oxidation takes place solely in peroxisomes. In this species, peroxisome biogenesis occurs when lipids are present in the culture medium, and it involves the Pex11p protein family: ScPex11p, ScPex25p, ScPex27p, and ScPex34p. Yarrowia lipolytica has three Pex11p homologues, which are YALI0C04092p (YlPex11p), YALI0C04565p (YlPex11C), and YALI0D25498p (Pex11/25p). We found that these genes are regulated by oleic acid, and as has been observed in other organisms, YlPEX11 deletion generated giant peroxisomes when mutant yeast were grown in oleic acid medium. Moreover, ΔYlpex11 was unable to grow on fatty acid medium and showed extreme dose-dependent sensitivity to oleic acid. Indeed, when the strain was grown in minimum medium with 0.5% glucose and 3% oleic acid, lipid body lysis and cell death were observed. Cell death and lipid body lysis may be partially explained by an imbalance in the expression of the genes involved in lipid storage, namely, DGA1, DGA2, and LRO1, as well as that of TGL4, which is involved in lipid remobilization. TGL4 deletion and DGA2 overexpression resulted in decreased oleic acid sensitivity and delayed cell death of ΔYlpex11, which probably stemmed from the release of free fatty acids into the cytoplasm. All these results show that YlPex11p plays an important role in lipid homeostasis in Y. lipolytica.
过氧化物酶体是大多数真核生物细胞中不可或缺的细胞器,从酵母到哺乳动物皆是如此。它们在β-氧化中的作用在酵母中尤为重要;例如,在酿酒酵母中,脂肪酸氧化仅发生在过氧化物酶体中。在该物种中,当过氧化物酶体生物发生在培养基中存在脂质时发生,并且涉及Pex11p蛋白家族:ScPex11p、ScPex25p、ScPex27p和ScPex34p。解脂耶氏酵母有三个Pex11p同源物,分别是YALI0C04092p(YlPex11p)、YALI0C04565p(YlPex11C)和YALI0D25498p(Pex11/25p)。我们发现这些基因受油酸调控,并且正如在其他生物体中所观察到的那样,当突变酵母在油酸培养基中生长时,YlPEX11缺失会产生巨大的过氧化物酶体。此外,ΔYlpex11无法在脂肪酸培养基上生长,并且对油酸表现出极端的剂量依赖性敏感性。实际上,当该菌株在含有0.5%葡萄糖和3%油酸的基本培养基中生长时,观察到脂质体裂解和细胞死亡。细胞死亡和脂质体裂解可能部分归因于参与脂质储存的基因(即DGA1、DGA2和LRO1)以及参与脂质转运的TGL4的表达失衡。TGL4缺失和DGA2过表达导致ΔYlpex11的油酸敏感性降低和细胞死亡延迟,这可能源于游离脂肪酸释放到细胞质中。所有这些结果表明,YlPex11p在解脂耶氏酵母的脂质稳态中起重要作用。