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鉴定与 SREBP 通路相关的潜在新基因。

Identification of Potential New Genes Related to the SREBP Pathway in .

机构信息

Departamento de Ciencias Ecológicas, Facultad de Ciencias, Universidad de Chile, Las Palmeras 3425, Santiago 7800003, Chile.

Facultad de Ciencias, Universidad de Chile, Las Palmeras 3425, Santiago 7800003, Chile.

出版信息

Biomolecules. 2024 Jun 29;14(7):778. doi: 10.3390/biom14070778.

Abstract

The sterol regulatory element-binding protein (SREBP) pathway is an integral cellular mechanism that regulates lipid homeostasis, in which transcriptional activator SREBPs regulate the expression of various genes. In the carotenogenic yeast , Sre1 (the yeast SREBP homolog) regulates lipid biosynthesis and carotenogenesis, among other processes. Despite the characterization of several components of the SREBP pathway across various eukaryotes, the specific elements of this pathway in remain largely unknown. This study aimed to explore the potential regulatory mechanisms of the SREBP pathway in using the strain CBS. as a model, which is known to have Sre1 in its active state under standard culture conditions, resulting in a carotenoid-overproducing phenotype. This strain was subjected to random mutagenesis with N-methyl-N'-nitro-N-nitrosoguanidine (NTG), followed by a screening methodology that focused on identifying mutants with altered Sre1 activation phenotypes. Single-nucleotide polymorphism (SNP) analysis of 20 selected mutants detected 5439 single-nucleotide variants (SNVs), narrowing them down to 1327 SNPs of interest after a series of filters. Classification based on SNP impact identified 116 candidate genes, including 49 genes with high impact and 68 genes with deleterious moderate-impact mutations. BLAST, InterProScan, and gene ontology enrichment analyses highlighted 25 genes as potential participants in regulating Sre1 in . The key findings of this study include the identification of genes potentially encoding proteins involved in protein import/export to the nucleus, sterol biosynthesis, the ubiquitin-proteasome system, protein regulatory activities such as deacetylases, a subset of kinases and proteases, as well as transcription factors that could be influential in SREBP regulation. These findings are expected to significantly contribute to the current understanding of the intricate regulation of the transcription factor Sre1 in , providing valuable groundwork for future research and potential biotechnological applications.

摘要

固醇调节元件结合蛋白(SREBP)途径是一种调节脂质稳态的细胞内机制,其中转录激活因子 SREBPs 调节各种基因的表达。在产类胡萝卜素酵母中,Sre1(酵母 SREBP 同源物)调节脂质生物合成和类胡萝卜素生成等过程。尽管在各种真核生物中已经对 SREBP 途径的几个组成部分进行了描述,但在 中该途径的具体元素在很大程度上仍然未知。本研究旨在使用已知在标准培养条件下处于激活状态的 Sre1 的 CBS 菌株作为模型,探索 SREBP 途径在 中的潜在调控机制,导致类胡萝卜素过度产生的表型。该菌株用 N-甲基-N'-硝基-N-亚硝基胍(NTG)进行随机诱变,然后采用一种筛选方法,重点鉴定 Sre1 激活表型改变的突变体。对 20 个选定突变体进行单核苷酸多态性(SNP)分析,检测到 5439 个单核苷酸变异(SNV),经过一系列筛选后,将其缩小到 1327 个感兴趣的 SNP。基于 SNP 影响的分类确定了 116 个候选基因,其中包括 49 个高影响基因和 68 个具有有害中效影响突变的基因。BLAST、InterProScan 和基因本体富集分析突出了 25 个可能参与调节 的 Sre1 的基因。本研究的关键发现包括鉴定出潜在编码参与核蛋白输入/输出、固醇生物合成、泛素-蛋白酶体系统、蛋白调节活性(如去乙酰化酶)、一组激酶和蛋白酶以及转录因子的蛋白质的基因,这些基因可能在 SREBP 调节中发挥作用。这些发现有望极大地促进对 的转录因子 Sre1 复杂调控的现有理解,为未来的研究和潜在的生物技术应用提供有价值的基础。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6441/11274570/cb104d1b1dd1/biomolecules-14-00778-g001.jpg

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