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人类感染的肠上皮细胞内共生菌属的端粒到端粒基因组组装。

Telomere-to-Telomere genome assemblies of human-infecting Encephalitozoon species.

机构信息

Department of Biology, Illinois Institute of Technology, Chicago, IL, USA.

出版信息

BMC Genomics. 2023 May 4;24(1):237. doi: 10.1186/s12864-023-09331-3.

Abstract

BACKGROUND

Microsporidia are diverse spore forming, fungal-related obligate intracellular pathogens infecting a wide range of hosts. This diversity is reflected at the genome level with sizes varying by an order of magnitude, ranging from less than 3 Mb in Encephalitozoon species (the smallest known in eukaryotes) to more than 50 Mb in Edhazardia spp. As a paradigm of genome reduction in eukaryotes, the small Encephalitozoon genomes have attracted much attention with investigations revealing gene dense, repeat- and intron-poor genomes characterized by a thorough pruning of molecular functions no longer relevant to their obligate intracellular lifestyle. However, because no Encephalitozoon genome has been sequenced from telomere-to-telomere and since no methylation data is available for these species, our understanding of their overall genetic and epigenetic architectures is incomplete.

METHODS

In this study, we sequenced the complete genomes from telomere-to-telomere of three human-infecting Encephalitozoon spp. -E. intestinalis ATCC 50506, E. hellem ATCC 50604 and E. cuniculi ATCC 50602- using short and long read platforms and leveraged the data generated as part of the sequencing process to investigate the presence of epigenetic markers in these genomes. We also used a mixture of sequence- and structure-based computational approaches, including protein structure prediction, to help identify which Encephalitozoon proteins are involved in telomere maintenance, epigenetic regulation, and heterochromatin formation.

RESULTS

The Encephalitozoon chromosomes were found capped by TTAGG 5-mer telomeric repeats followed by telomere associated repeat elements (TAREs) flanking hypermethylated ribosomal RNA (rRNA) gene loci featuring 5-methylcytosines (5mC) and 5-hemimethylcytosines (5hmC), themselves followed by lesser methylated subtelomeres and hypomethylated chromosome cores. Strong nucleotide biases were identified between the telomeres/subtelomeres and chromosome cores with significant changes in GC/AT, GT/AC and GA/CT contents. The presence of several genes coding for proteins essential to telomere maintenance, epigenetic regulation, and heterochromatin formation was further confirmed in the Encephalitozoon genomes.

CONCLUSION

Altogether, our results strongly support the subtelomeres as sites of heterochromatin formation in Encephalitozoon genomes and further suggest that these species might shutdown their energy-consuming ribosomal machinery while dormant as spores by silencing of the rRNA genes using both 5mC/5hmC methylation and facultative heterochromatin formation at these loci.

摘要

背景

微孢子虫是一种多样化的孢子形成的真菌相关专性细胞内病原体,感染范围广泛的宿主。这种多样性在基因组水平上反映出来,大小相差一个数量级,从不到 3 Mb 的脑炎原生动物物种(真核生物中已知最小的)到超过 50 Mb 的埃达瓦迪亚属物种。作为真核生物中基因组减少的典范,小的脑炎原生动物基因组引起了广泛关注,研究表明它们的基因组密集、重复和内含子少,特征是对不再与其专性细胞内生活方式相关的分子功能进行了彻底的修剪。然而,由于没有从端粒到端粒测序的脑炎原生动物基因组,并且这些物种没有甲基化数据,我们对它们的整体遗传和表观遗传结构的理解并不完整。

方法

在这项研究中,我们使用短读和长读平台从端粒到端粒测序了三种感染人类的脑炎原生动物物种——E. intestinalis ATCC 50506、E. hellem ATCC 50604 和 E. cuniculi ATCC 50602——的完整基因组,并利用测序过程中生成的数据来研究这些基因组中是否存在表观遗传标记。我们还使用了一系列基于序列和结构的计算方法,包括蛋白质结构预测,来帮助确定哪些脑炎原生动物蛋白参与端粒维持、表观遗传调控和异染色质形成。

结果

脑炎原生动物染色体的 5 个末端被 TTAGG 5 个碱基的端粒重复序列所封闭,然后是端粒相关重复元件(TAREs),这些元件侧翼是富含 5-甲基胞嘧啶(5mC)和 5-羟甲基胞嘧啶(5hmC)的核糖体 RNA(rRNA)基因座,自身紧随其后的是甲基化程度较低的亚端粒和低甲基化的染色体核心。在端粒/亚端粒和染色体核心之间发现了强烈的核苷酸偏倚,GC/AT、GT/AC 和 GA/CT 含量有显著变化。在脑炎原生动物基因组中进一步证实了几个编码端粒维持、表观遗传调控和异染色质形成所必需蛋白的基因的存在。

结论

总的来说,我们的结果强烈支持在脑炎原生动物基因组中,亚端粒是异染色质形成的部位,并进一步表明这些物种在休眠时作为孢子可能会通过 rRNA 基因的 5mC/5hmC 甲基化和这些位点的兼性异染色质形成来沉默核糖体机制,从而关闭其耗能的核糖体机制。

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