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AMPKα 亚基 Ssp2 和糖原合成酶激酶 Gsk3/Gsk31 参与了裂殖酵母固醇调节元件结合蛋白 (SREBP) 活性的调节。

AMPKα Subunit Ssp2 and Glycogen Synthase Kinases Gsk3/Gsk31 are involved in regulation of sterol regulatory element-binding protein (SREBP) activity in fission yeast.

机构信息

Department of Microbial and Biochemical Pharmacy, School of Pharmacy, China Medical University, Shenyang, Liaoning Province, China.

Division of Food and Drug Evaluation Science, Kobe University Graduate School of Medicine, Kobe, Japan.

出版信息

PLoS One. 2020 Feb 13;15(2):e0228845. doi: 10.1371/journal.pone.0228845. eCollection 2020.

Abstract

Sterol regulatory element-binding protein (SREBP), a highly conserved family of membrane-bound transcription factors, is an essential regulator for cellular cholesterol and lipid homeostasis in mammalian cells. Sre1, the homolog of SREBP in the fission yeast Schizosaccharomyces pombe (S. pombe), regulates genes involved in the transcriptional responses to low sterol as well as low oxygen. Previous study reported that casein kinase 1 family member Hhp2 phosphorylated the Sre1 N-terminal transcriptional factor domain (Sre1N) and accelerated Sre1N degradation, and other kinases might exist for regulating the Sre1 function. To gain insight into the mechanisms underlying the Sre1 activity and to identify additional kinases involved in regulation of Sre1 function, we developed a luciferase reporter system to monitor the Sre1 activity through its binding site called SRE2 in living yeast cells. Here we showed that both ergosterol biosynthesis inhibitors and hypoxia-mimic CoCl2 caused a dose-dependent increase in the Sre1 transcription activity, concurrently, these induced transcription activities were almost abolished in Δsre1 cells. Surprisingly, either AMPKα Subunit Ssp2 deletion or Glycogen Synthase Kinases Gsk3/Gsk31 double deletion significantly suppressed ergosterol biosynthesis inhibitors- or CoCl2-induced Sre1 activity. Notably, the Δssp2Δgsk3Δgsk31 mutant showed further decreased Sre1 activity when compared with their single or double deletion. Consistently, the Δssp2Δgsk3Δgsk31 mutant showed more marked temperature sensitivity than any of their single or double deletion. Moreover, the fluorescence of GFP-Sre1N localized at the nucleus in wild-type cells, but significantly weaker nuclear fluorescence of GFP-Sre1N was observed in Δssp2, Δgsk3Δgsk31, Δssp2Δgsk3, Δssp2Δgsk31 or Δssp2Δgsk3Δgsk31 cells. On the other hand, the immunoblot showed a dramatic decrease in GST-Sre1N levels in the Δgsk3Δgsk31 or the Δssp2Δgsk3Δgsk31 cells but not in the Δssp2 cells. Altogether, our findings suggest that Gsk3/Gsk31 may regulate Sre1N degradation, while Ssp2 may regulate not only the degradation of Sre1N but also its translocation to the nucleus.

摘要

固醇调节元件结合蛋白(SREBP)是一个高度保守的膜结合转录因子家族,是哺乳动物细胞中细胞胆固醇和脂质稳态的重要调节剂。裂殖酵母 Schizosaccharomyces pombe(S. pombe)中的 Sre1 同源物是 SREBP 的同源物,它调节参与低固醇和低氧转录反应的基因。先前的研究表明,酪蛋白激酶 1 家族成员 Hhp2 磷酸化 Sre1 N 端转录因子结构域(Sre1N)并加速 Sre1N 降解,并且可能存在其他激酶来调节 Sre1 功能。为了深入了解 Sre1 活性的机制,并确定参与 Sre1 功能调节的其他激酶,我们开发了一种荧光素酶报告系统,通过其在活酵母细胞中的结合位点 SRE2 来监测 Sre1 活性。在这里,我们发现,麦角固醇生物合成抑制剂和缺氧模拟物 CoCl2 都导致 Sre1 转录活性呈剂量依赖性增加,同时,这些诱导的转录活性在Δsre1 细胞中几乎被消除。令人惊讶的是,AMPKα 亚基 Ssp2 缺失或糖原合酶激酶 Gsk3/Gsk31 双缺失显著抑制了麦角固醇生物合成抑制剂或 CoCl2 诱导的 Sre1 活性。值得注意的是,与单或双缺失相比,Δssp2Δgsk3Δgsk31 突变体显示出进一步降低的 Sre1 活性。一致地,与任何单或双缺失体相比,Δssp2Δgsk3Δgsk31 突变体表现出更明显的温度敏感性。此外,GFP-Sre1N 的荧光在野生型细胞中定位于细胞核,但在Δssp2、Δgsk3Δgsk31、Δssp2Δgsk3、Δssp2Δgsk31 或Δssp2Δgsk3Δgsk31 细胞中观察到 GFP-Sre1N 的核荧光明显减弱。另一方面,免疫印迹显示,GST-Sre1N 水平在Δgsk3Δgsk31 或Δssp2Δgsk3Δgsk31 细胞中急剧下降,但在Δssp2 细胞中没有下降。总之,我们的发现表明,Gsk3/Gsk31 可能调节 Sre1N 的降解,而 Ssp2 可能不仅调节 Sre1N 的降解,还调节其向核内的易位。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1c36/7018046/4222ec629c2b/pone.0228845.g001.jpg

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