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首页> 外文期刊>Genes and genomics >Transcriptome analysis of Delta mig1 Delta mig2 mutant reveals their roles in methanol catabolism, peroxisome biogenesis and autophagy in methylotrophic yeast Pichia pastoris
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Transcriptome analysis of Delta mig1 Delta mig2 mutant reveals their roles in methanol catabolism, peroxisome biogenesis and autophagy in methylotrophic yeast Pichia pastoris

机译:Delta mig1 delta mig2突变体的转录组分析揭示了它们在甲醇分解代谢,过氧缺血性生物发生和甲基嗜型酵母酵母酵母碱基碱

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摘要

Two catabolite repressor genes (MIG1 and MIG2) were previously identified in Pichia pastoris, and the derepression of alcohol oxidase (AOX) expression was realized in Delta mig1 or Delta mig1 Delta mig2 mutants grown in glycerol, but not in glucose. In this study, genome-wide RNA-seq analysis of Delta mig1 Delta mig2 and the wild-type strain grown in glycerol revealed that the expression of numerous genes was greatly altered. Nearly 7% (357 genes) of approximately 5276 genes annotated in P. pastoris were significantly upregulated, with at least a two-fold differential expression in Delta mig1 Delta mig2; the genes were mainly related to cell metabolism. Approximately 23% (1197 genes) were significantly downregulated; these were mainly correlated with the physiological characteristics of the cell. The methanol catabolism and peroxisome biogenesis pathways were remarkably enhanced, and the genes AOX1 and AOX2 were upregulated higher than 30-fold, which was consistent with the experimental results of AOX expression. The Mig proteins had a slight effect on autophagy when cells were grown in glycerol. The expression analysis of transcription factors showed that deletion of MIG1 and MIG2 significantly upregulated the binding of an essential transcription activator, Mit1p, with the AOX1 promoter, which suggested that Mig proteins might regulate the AOX1 promoter through the regulation of Mit1p. This work provides a reference for the further exploration of the methanol induction and catabolite repression mechanisms of AOX expression in methylotrophic yeasts.
机译:先前在Pichia Pastoris中鉴定了两种分层压缩机基因(MIG1和MIG2),并且在甘油中生长的Delta Mig1或Delta Mig1 Delta Mig2突变体中实现了醇氧化酶(AOX)表达的DEREPRIANG,但不在葡萄糖中实现。在该研究中,甘油中达到ΔMig1δmig2的基因组RNA-SEQ分析和甘油中生长的野生型菌株显示出大量改变了许多基因的表达。在P. Pastoris中注释的近7%(357个基因)显着上调,在Delta mig1 delta mig2中至少具有两倍的差异表达;该基因主要与细胞代谢有关。大约23%(1197个基因)明显下调;这些主要与细胞的生理特性相关。甲醇分解代谢和过氧化物体生物发生途径显着增强,并且基因AOX1和AOX2上调高于30倍,这与AX表达的实验结果一致。当细胞在甘油中生长细胞时,MIG蛋白对自噬有轻微的影响。转录因子的表达分析表明,MIG1和MIG2的缺失显着上调了必需转录活化剂,MIT1P与AOX1启动子的结合,这表明MIG蛋白可以通过MIT1P调节调节AOX1启动子。这项工作提供了进一步探索甲基营养酵母中αox表达的甲醇诱导和分解代谢抑制机制的参考。

著录项

  • 来源
    《Genes and genomics》 |2018年第4期|共14页
  • 作者单位

    East China Univ Sci &

    Technol State Key Lab Bioreactor Engn Shanghai 200237 Peoples R China;

    East China Univ Sci &

    Technol State Key Lab Bioreactor Engn Shanghai 200237 Peoples R China;

    East China Univ Sci &

    Technol State Key Lab Bioreactor Engn Shanghai 200237 Peoples R China;

    East China Univ Sci &

    Technol State Key Lab Bioreactor Engn Shanghai 200237 Peoples R China;

    East China Univ Sci &

    Technol State Key Lab Bioreactor Engn Shanghai 200237 Peoples R China;

    East China Univ Sci &

    Technol State Key Lab Bioreactor Engn Shanghai 200237 Peoples R China;

    East China Univ Sci &

    Technol State Key Lab Bioreactor Engn Shanghai 200237 Peoples R China;

    East China Univ Sci &

    Technol State Key Lab Bioreactor Engn Shanghai 200237 Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 生物科学;
  • 关键词

    Pichia pastoris; RNA-seq; Mig; Alcohol oxidase; Catabolite repression;

    机译:Pichia Pastoris;RNA-SEQ;mig;酒精氧化酶;抗粘土抑制;

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