蓝藻中 m4C DNA 甲基化对四吡咯生物合成的表观遗传控制

Nils Schmidt, Nils Stappert, Kaori Nimura-Matsune, Satoru Watanabe, Roman Sobotka, Martin Hagemann, Wolfgang R. Hess
{"title":"蓝藻中 m4C DNA 甲基化对四吡咯生物合成的表观遗传控制","authors":"Nils Schmidt, Nils Stappert, Kaori Nimura-Matsune, Satoru Watanabe, Roman Sobotka, Martin Hagemann, Wolfgang R. Hess","doi":"10.1101/2024.08.20.608618","DOIUrl":null,"url":null,"abstract":"Epigenetic DNA modifications are pivotal in eukaryotic gene expression, but their regulatory significance in bacteria is less understood. In Synechocystis 6803, the DNA methyltransferase M.Ssp6803II modifies the first cytosine in the GGCC motif, forming N4-methylcytosine (GGm4CC). Deleting the sll0729 gene (deltall0729) caused a bluish phenotype due to reduced chlorophyll levels, which was reversed by suppressor mutations. Re-sequencing of seven suppressor clones revealed a common GGCC to GGTC mutation in the slr1790 promoter's discriminator sequence, encoding protoporphyrinogen IX oxidase, HemJ, crucial for tetrapyrrole biosynthesis. Transcriptomic and qPCR analyses indicated aberrant slr1790 expression in deltall0729 mutants. This aberration led to the accumulation of coprotoporphyrin III and protoporphyrin IX, indicative of impaired HemJ activity. To confirm the importance of DNA methylation in hemJ expression, native and mutated hemJ promoter variants were introduced into the wild type, followed by sll0729 deletion. The sll0729 deletion segregated in strains with the GGTC motif in the hemJ promoter, resulting in wild-type-like pigmentation, whereas freshly prepared deltall0729 mutants with the native hemJ promoter exhibited the bluish phenotype. These findings demonstrate that hemJ is tightly regulated in Synechocystis and that N4-methylcytosine is essential for proper hemJ expression.","PeriodicalId":501357,"journal":{"name":"bioRxiv - Microbiology","volume":null,"pages":null},"PeriodicalIF":0.0000,"publicationDate":"2024-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Epigenetic control of tetrapyrrole biosynthesis by m4C DNA methylation in a cyanobacterium\",\"authors\":\"Nils Schmidt, Nils Stappert, Kaori Nimura-Matsune, Satoru Watanabe, Roman Sobotka, Martin Hagemann, Wolfgang R. Hess\",\"doi\":\"10.1101/2024.08.20.608618\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Epigenetic DNA modifications are pivotal in eukaryotic gene expression, but their regulatory significance in bacteria is less understood. In Synechocystis 6803, the DNA methyltransferase M.Ssp6803II modifies the first cytosine in the GGCC motif, forming N4-methylcytosine (GGm4CC). Deleting the sll0729 gene (deltall0729) caused a bluish phenotype due to reduced chlorophyll levels, which was reversed by suppressor mutations. Re-sequencing of seven suppressor clones revealed a common GGCC to GGTC mutation in the slr1790 promoter's discriminator sequence, encoding protoporphyrinogen IX oxidase, HemJ, crucial for tetrapyrrole biosynthesis. Transcriptomic and qPCR analyses indicated aberrant slr1790 expression in deltall0729 mutants. This aberration led to the accumulation of coprotoporphyrin III and protoporphyrin IX, indicative of impaired HemJ activity. To confirm the importance of DNA methylation in hemJ expression, native and mutated hemJ promoter variants were introduced into the wild type, followed by sll0729 deletion. The sll0729 deletion segregated in strains with the GGTC motif in the hemJ promoter, resulting in wild-type-like pigmentation, whereas freshly prepared deltall0729 mutants with the native hemJ promoter exhibited the bluish phenotype. These findings demonstrate that hemJ is tightly regulated in Synechocystis and that N4-methylcytosine is essential for proper hemJ expression.\",\"PeriodicalId\":501357,\"journal\":{\"name\":\"bioRxiv - Microbiology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-09-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"bioRxiv - Microbiology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1101/2024.08.20.608618\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"bioRxiv - Microbiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1101/2024.08.20.608618","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

表观遗传 DNA 修饰在真核生物基因表达中起着关键作用,但它们在细菌中的调控意义却鲜为人知。在 Synechocystis 6803 中,DNA 甲基转移酶 M.Ssp6803II 会修饰 GGCC 矩阵中的第一个胞嘧啶,形成 N4-甲基胞嘧啶(GGm4CC)。删除 sll0729 基因(deltall0729)会导致叶绿素水平降低而出现蓝色表型,而抑制基因突变可逆转这种表型。对 7 个抑制基因克隆重新测序后发现,在 slr1790 启动子的鉴别序列中存在一个由 GGCC 到 GGTC 的共同突变,该基因编码原卟啉原 IX 氧化酶 HemJ,对四吡咯的生物合成至关重要。转录组和 qPCR 分析表明,在 deltall0729 突变体中,slr1790 表达异常。这种异常导致共卟啉 III 和原卟啉 IX 的积累,表明 HemJ 活性受损。为了证实DNA甲基化在hemJ表达中的重要性,将原生和突变的hemJ启动子变体引入野生型,然后进行sll0729缺失。sll0729缺失在带有hemJ启动子中GGTC基序的菌株中发生分离,导致类似野生型的色素沉着,而带有原生hemJ启动子的新鲜制备的deltall0729突变体则表现出蓝色表型。这些发现表明,hemJ 在 Synechocystis 中受到严格调控,而 N4-甲基胞嘧啶是正常表达 hemJ 的必要条件。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Epigenetic control of tetrapyrrole biosynthesis by m4C DNA methylation in a cyanobacterium
Epigenetic DNA modifications are pivotal in eukaryotic gene expression, but their regulatory significance in bacteria is less understood. In Synechocystis 6803, the DNA methyltransferase M.Ssp6803II modifies the first cytosine in the GGCC motif, forming N4-methylcytosine (GGm4CC). Deleting the sll0729 gene (deltall0729) caused a bluish phenotype due to reduced chlorophyll levels, which was reversed by suppressor mutations. Re-sequencing of seven suppressor clones revealed a common GGCC to GGTC mutation in the slr1790 promoter's discriminator sequence, encoding protoporphyrinogen IX oxidase, HemJ, crucial for tetrapyrrole biosynthesis. Transcriptomic and qPCR analyses indicated aberrant slr1790 expression in deltall0729 mutants. This aberration led to the accumulation of coprotoporphyrin III and protoporphyrin IX, indicative of impaired HemJ activity. To confirm the importance of DNA methylation in hemJ expression, native and mutated hemJ promoter variants were introduced into the wild type, followed by sll0729 deletion. The sll0729 deletion segregated in strains with the GGTC motif in the hemJ promoter, resulting in wild-type-like pigmentation, whereas freshly prepared deltall0729 mutants with the native hemJ promoter exhibited the bluish phenotype. These findings demonstrate that hemJ is tightly regulated in Synechocystis and that N4-methylcytosine is essential for proper hemJ expression.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信