Diana L. Bordin , Kayla Grooms , Nicola P. Montaldo , Sarah L. Fordyce Martin , Pål Sætrom , Leona D. Samson , Magnar Bjørås , Barbara van Loon
{"title":"\"烷基腺嘌呤 DNA 糖基化酶的缺失会改变发育中小鼠大脑的基因表达,并导致焦虑减少和记忆力增强\"","authors":"Diana L. Bordin , Kayla Grooms , Nicola P. Montaldo , Sarah L. Fordyce Martin , Pål Sætrom , Leona D. Samson , Magnar Bjørås , Barbara van Loon","doi":"10.1016/j.dnarep.2024.103632","DOIUrl":null,"url":null,"abstract":"<div><p>Neurodevelopment is a tightly coordinated process, during which the genome is exposed to spectra of endogenous agents at different stages of differentiation. Emerging evidence indicates that DNA damage is an important feature of developing brain, tightly linked to gene expression and neuronal activity. Some of the most frequent DNA damage includes changes to DNA bases, which are recognized by DNA glycosylases and repaired through base excision repair (BER) pathway. The only mammalian DNA glycosylase able to remove frequent alkylated DNA based is alkyladenine DNA glycosylase (Aag, aka Mpg). We recently demonstrated that, besides its role in DNA repair, AAG affects expression of neurodevelopmental genes in human cells. Aag was further proposed to act as reader of epigenetic marks, including 5-hydroxymethylcytosine (5hmC), in the mouse brain. Despite the potential Aag involvement in the key brain processes, the impact of Aag loss on developing brain remains unknown. Here, by using Aag knockout (<em>Aag</em><sup><em>-/-</em></sup>) mice, we show that Aag absence leads to reduced DNA break levels, evident in lowered number of γH2AX foci in postnatal day 5 (P5) hippocampi. This is accompanied by changes in 5hmC signal intensity in different hippocampal regions. Transcriptome analysis of hippocampi and prefrontal cortex, at different developmental stages, indicates that lack of Aag alters gene expression, primarily of genes involved in regulation of response to stress. Across all developmental stages tested aldehyde dehydrogenase 2 (<em>Aldh2</em>) emerged as one of the most prominent genes deregulated in Aag-dependent manner. In line with the changes in hippocampal DNA damage levels and the gene expression, adult <em>Aag</em><sup><em>-/-</em></sup> mice exhibit altered behavior, evident in decreased anxiety levels determined in the Elevated Zero Maze and increased alternations in the Elevated T Maze tests. Taken together these results suggests that Aag has functions in modulation of genome dynamics during brain development, important for animal behavior.</p></div>","PeriodicalId":300,"journal":{"name":"DNA Repair","volume":"135 ","pages":"Article 103632"},"PeriodicalIF":3.0000,"publicationDate":"2024-01-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.sciencedirect.com/science/article/pii/S1568786424000089/pdfft?md5=dfe89041e60b27b790f705d233362d1d&pid=1-s2.0-S1568786424000089-main.pdf","citationCount":"0","resultStr":"{\"title\":\"Loss of alkyladenine DNA glycosylase alters gene expression in the developing mouse brain and leads to reduced anxiety and improved memory\",\"authors\":\"Diana L. Bordin , Kayla Grooms , Nicola P. Montaldo , Sarah L. Fordyce Martin , Pål Sætrom , Leona D. Samson , Magnar Bjørås , Barbara van Loon\",\"doi\":\"10.1016/j.dnarep.2024.103632\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Neurodevelopment is a tightly coordinated process, during which the genome is exposed to spectra of endogenous agents at different stages of differentiation. Emerging evidence indicates that DNA damage is an important feature of developing brain, tightly linked to gene expression and neuronal activity. Some of the most frequent DNA damage includes changes to DNA bases, which are recognized by DNA glycosylases and repaired through base excision repair (BER) pathway. The only mammalian DNA glycosylase able to remove frequent alkylated DNA based is alkyladenine DNA glycosylase (Aag, aka Mpg). We recently demonstrated that, besides its role in DNA repair, AAG affects expression of neurodevelopmental genes in human cells. Aag was further proposed to act as reader of epigenetic marks, including 5-hydroxymethylcytosine (5hmC), in the mouse brain. Despite the potential Aag involvement in the key brain processes, the impact of Aag loss on developing brain remains unknown. Here, by using Aag knockout (<em>Aag</em><sup><em>-/-</em></sup>) mice, we show that Aag absence leads to reduced DNA break levels, evident in lowered number of γH2AX foci in postnatal day 5 (P5) hippocampi. This is accompanied by changes in 5hmC signal intensity in different hippocampal regions. Transcriptome analysis of hippocampi and prefrontal cortex, at different developmental stages, indicates that lack of Aag alters gene expression, primarily of genes involved in regulation of response to stress. Across all developmental stages tested aldehyde dehydrogenase 2 (<em>Aldh2</em>) emerged as one of the most prominent genes deregulated in Aag-dependent manner. In line with the changes in hippocampal DNA damage levels and the gene expression, adult <em>Aag</em><sup><em>-/-</em></sup> mice exhibit altered behavior, evident in decreased anxiety levels determined in the Elevated Zero Maze and increased alternations in the Elevated T Maze tests. 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引用次数: 0
摘要
神经系统的发育是一个紧密协调的过程,在这一过程中,基因组在不同的分化阶段会受到各种内源因子的影响。新的证据表明,DNA 损伤是大脑发育的一个重要特征,与基因表达和神经元活动密切相关。一些最常见的 DNA 损伤包括 DNA 碱基的改变,这些改变会被 DNA 糖基化酶识别,并通过碱基切除修复(BER)途径进行修复。哺乳动物 DNA 糖基化酶中唯一能去除频繁发生的烷基化 DNA 碱基的是烷基腺嘌呤 DNA 糖基化酶(Aag,又名 Mpg)。我们最近证实,除了在 DNA 修复中发挥作用外,AAG 还会影响人类细胞中神经发育基因的表达。我们还进一步提出,Aag 是小鼠大脑中包括 5-羟甲基胞嘧啶(5hmC)在内的表观遗传标记的阅读器。尽管Aag可能参与了大脑的关键过程,但Aag缺失对发育中大脑的影响仍然未知。在这里,通过使用 Aag 基因敲除(Aag-/-)小鼠,我们发现 Aag 缺失会导致 DNA 断裂水平降低,这在出生后第 5 天(P5)海马中的γH2AX 病灶数量减少上很明显。与此同时,不同海马区的 5hmC 信号强度也发生了变化。对不同发育阶段的海马和前额叶皮层进行的转录组分析表明,缺乏 Aag 会改变基因的表达,主要是参与调控应激反应的基因。在测试的所有发育阶段中,醛脱氢酶 2(Aldh2)是最主要的基因之一,其表达受 Aag 依赖性影响。与海马 DNA 损伤水平和基因表达的变化相一致,成年 Aag-/- 小鼠的行为也发生了改变,这表现在高架零迷宫中焦虑水平的降低和高架 T 型迷宫测试中交替行为的增加。综上所述,这些结果表明,Aag 在大脑发育过程中具有调节基因组动态的功能,这对动物行为非常重要。
Loss of alkyladenine DNA glycosylase alters gene expression in the developing mouse brain and leads to reduced anxiety and improved memory
Neurodevelopment is a tightly coordinated process, during which the genome is exposed to spectra of endogenous agents at different stages of differentiation. Emerging evidence indicates that DNA damage is an important feature of developing brain, tightly linked to gene expression and neuronal activity. Some of the most frequent DNA damage includes changes to DNA bases, which are recognized by DNA glycosylases and repaired through base excision repair (BER) pathway. The only mammalian DNA glycosylase able to remove frequent alkylated DNA based is alkyladenine DNA glycosylase (Aag, aka Mpg). We recently demonstrated that, besides its role in DNA repair, AAG affects expression of neurodevelopmental genes in human cells. Aag was further proposed to act as reader of epigenetic marks, including 5-hydroxymethylcytosine (5hmC), in the mouse brain. Despite the potential Aag involvement in the key brain processes, the impact of Aag loss on developing brain remains unknown. Here, by using Aag knockout (Aag-/-) mice, we show that Aag absence leads to reduced DNA break levels, evident in lowered number of γH2AX foci in postnatal day 5 (P5) hippocampi. This is accompanied by changes in 5hmC signal intensity in different hippocampal regions. Transcriptome analysis of hippocampi and prefrontal cortex, at different developmental stages, indicates that lack of Aag alters gene expression, primarily of genes involved in regulation of response to stress. Across all developmental stages tested aldehyde dehydrogenase 2 (Aldh2) emerged as one of the most prominent genes deregulated in Aag-dependent manner. In line with the changes in hippocampal DNA damage levels and the gene expression, adult Aag-/- mice exhibit altered behavior, evident in decreased anxiety levels determined in the Elevated Zero Maze and increased alternations in the Elevated T Maze tests. Taken together these results suggests that Aag has functions in modulation of genome dynamics during brain development, important for animal behavior.
期刊介绍:
DNA Repair provides a forum for the comprehensive coverage of DNA repair and cellular responses to DNA damage. The journal publishes original observations on genetic, cellular, biochemical, structural and molecular aspects of DNA repair, mutagenesis, cell cycle regulation, apoptosis and other biological responses in cells exposed to genomic insult, as well as their relationship to human disease.
DNA Repair publishes full-length research articles, brief reports on research, and reviews. The journal welcomes articles describing databases, methods and new technologies supporting research on DNA repair and responses to DNA damage. Letters to the Editor, hot topics and classics in DNA repair, historical reflections, book reviews and meeting reports also will be considered for publication.