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抗坏血酸过氧化物酶 4 参与莱茵衣藻耐受光氧化胁迫。

Ascorbate peroxidase 4 plays a role in the tolerance of Chlamydomonas reinhardtii to photo-oxidative stress.

机构信息

Department of Marine Biotechnology and Resources, National Sun Yat-Sen University, Kaohsiung, 80424, Taiwan.

Doctoral Degree Program in Marine Biotechnology, National Sun Yat-Sen University, Kaohsiung, 80424, Taiwan.

出版信息

Sci Rep. 2020 Aug 6;10(1):13287. doi: 10.1038/s41598-020-70247-z.

Abstract

Ascorbate peroxidase (APX; EC 1.11.1.11) activity and transcript levels of CrAPX1, CrAPX2, and CrAPX4 of Chlamydomonas reinhardtii increased under 1,400 μE·m·s condition (HL). CrAPX4 expression was the most significant. So, CrAPX4 was downregulated using amiRNA technology to examine the role of APX for HL acclimation. The CrAPX4 knockdown amiRNA lines showed low APX activity and CrAPX4 transcript level without a change in CrAPX1 and CrAPX2 transcript levels, and monodehydroascorbate reductase (MDAR), dehydroascorbate reductase (DHAR), and glutathione reductase (GR) activities and transcript levels. Upon exposure to HL, CrAPX4 knockdown amiRNA lines appeared a modification in the expression of genes encoding the enzymes in the ascorbate-glutathione cycle, including an increase in transcript level of CrVTC2, a key enzyme for ascorbate (AsA) biosynthesis but a decrease in MDAR and DHAR transcription and activity after 1 h, followed by increases in reactive oxygen species production and lipid peroxidation after 6 h and exhibited cell death after 9 h. Besides, AsA content and AsA/DHA (dehydroascorbate) ratio decreased in CrAPX4 knockdown amiRNA lines after prolonged HL treatment. Thus, CrAPX4 induction together with its association with the modulation of MDAR and DHAR expression for AsA regeneration is critical for Chlamydomonas to cope with photo-oxidative stress.

摘要

抗坏血酸过氧化物酶(APX;EC 1.11.1.11)活性和莱茵衣藻 CrAPX1、CrAPX2 和 CrAPX4 的转录水平在 1400 μE·m·s 条件(HL)下增加。CrAPX4 的表达最为显著。因此,使用 amiRNA 技术下调 CrAPX4 的表达,以研究 APX 在 HL 适应中的作用。CrAPX4 敲低 amiRNA 系表现出低 APX 活性和 CrAPX4 转录水平,而 CrAPX1 和 CrAPX2 转录水平没有变化,并且单脱氢抗坏血酸还原酶(MDAR)、脱氢抗坏血酸还原酶(DHAR)和谷胱甘肽还原酶(GR)活性和转录水平没有变化。在暴露于 HL 后,CrAPX4 敲低 amiRNA 系表现出参与抗坏血酸-谷胱甘肽循环的酶编码基因的表达修饰,包括关键酶 CrVTC2 的转录水平增加,但 MDAR 和 DHAR 的转录和活性在 1 小时后降低,随后在 6 小时后产生更多的活性氧物质和脂质过氧化,并且在 9 小时后出现细胞死亡。此外,在长时间 HL 处理后,CrAPX4 敲低 amiRNA 系中的抗坏血酸含量和抗坏血酸/脱氢抗坏血酸(DHA)比降低。因此,CrAPX4 的诱导及其与 MDAR 和 DHAR 表达的调节一起,对于莱茵衣藻应对光氧化应激至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/786d/7414030/c3b8e24210c4/41598_2020_70247_Fig1_HTML.jpg

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